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Acneiform eruptions in dermatology : a differential diagnosis

https://libcat.nshealth.ca/en/permalink/provcat33764
Joshua A. Zeichner, editor. --New York: Springer , c2014.
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Dermatologists commonly treat acne, which affects 40 to 50 million Americans each year and about 85 percent of all patients at some point in their lives. Dermatologists, primary care doctors, and pediatricians see these patients every day in practice. It is important to treat the skin effectively not only to reduce the risk of physical scarring, but also to address the negative psychosocial impact this disease carries. Improving the skin can improve self-confidence, interpersonal relationships,…
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Other Authors
Zeichner, Joshua
Responsibility
Joshua A. Zeichner, editor
Place of Publication
New York
Publisher
Springer
Date of Publication
c2014
Physical Description
1 online resource (xxi, 418 pages)
ISBN
9781461483441 (electronic bk.)
9781461483434
Subjects (MeSH)
Acne Vulgaris - diagnosis
Acne Vulgaris - therapy
Acneiform Eruptions
Diagnosis, Differential
Skin Diseases - diagnosis
Skin Diseases - therapy
Skin Manifestations
Subjects (LCSH)
Acne - Diagnosis
Acne Vulgaris - diagnosis
Dermatology
Abstract
Dermatologists commonly treat acne, which affects 40 to 50 million Americans each year and about 85 percent of all patients at some point in their lives. Dermatologists, primary care doctors, and pediatricians see these patients every day in practice. It is important to treat the skin effectively not only to reduce the risk of physical scarring, but also to address the negative psychosocial impact this disease carries. Improving the skin can improve self-confidence, interpersonal relationships, and performance in school or at work. Acneiform Eruptions in Dermatology is a practical, full-color guide to the differential diagnosis of acne vulgaris and the treatment of acne-like conditions. It is organized into sections by subtype of condition (e.g., infections, genetic syndromes, medication-caused) and includes a section of variants of acne that may be misdiagnosed. Within the sections, individual chapters discuss each variant of the condition and begin with a helpful bulleted summary of its defining clinical features. Extensive color clinical images appear throughout the book.
Contents
Part I. Acne Vulgaris -- 1. Acne Pathophysiology -- 2. Clinical Presentation of Acne -- 3. Topical Therapies for Acne -- 4. Systemic Therapies for Acne -- 5. Laser and Light Based Therapies for Acne -- Part II. Infectious Diseases Mimicking Acne Vulgaris -- 6. Bacterial Folliculitis -- 7. Gram Negative Folliculitis -- 8. Hot Tub Folliculitis -- 9. Pityrosporum Folliculitis -- 10. Tinea Barbae -- 11. Flat Warts -- 12. Molluscum Contagiosum -- 13. Herpes Simplex Virus -- 14. Varicella Zoster Virus -- Part III. Variants of Acne Vulgaris -- 15. Acne Conglobata -- 16. Acne Excoriee -- 17. Acne Fulminans -- 18. Acne Mechanica -- 19. Cushing Syndrome -- 20. PAPA Syndrome -- 21. Polycystic Ovary Syndrome -- 22. Pomade Acne -- 23. Post-Adolescent Female Acne -- 24. SAPHO Syndrome -- Part IV. Genetic Syndromes Mimicking Acne Vulgaris -- 25. Apert Syndrome -- 26. Birt Hogg Dube Syndrome -- 27. Brooke Spiegler Syndrome -- 28. Cowden Syndrome -- 29. Gardner Syndrome -- 30. Gorlin Syndrome -- 31. Muir Torre Syndrome -- 32. Reed Syndrome -- 33. Tuberous Sclerosis -- Part V. Other Mimickers of Acne Vulgaris -- 34. Acne Scarring -- 35. Eosinophilic Pustular Folliculitis -- 36. Favre Racouchot -- 37. Hidradenitis Suppurativa -- 38. Perioral Dermatitis -- 39. Photocontact Dermatitis -- 40. Postinflammatory Pigmetnation -- 41. Pseudofolliculitis Barbae -- 42. Pustular Psoriasis -- 43. Rosacea -- 44. Rosacea Fulminans -- 45. Sarcoidosis -- 46. Seborrheic Dermatitis -- 47. Steatocystoma Multiplex -- 48. Xanthomas -- Part VI. Pediatric Dermatoses Mimicking Acne -- 49. Periorifical Granulomatous Dermatitis -- 50. Keratosis Pilaris Atrophicans -- 51. Neonatal and Infantile Acne -- 52. Papular Granuloma Annulare -- 53. Precocious Puberty -- Part VII. Drug Induced Acneiform Eruptions -- 54. Drug Induced Acneiform Eruptions.
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e-Book
Location
Online
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Adolescent Nutrition : Assuring the Needs of Emerging Adults

https://libcat.nshealth.ca/en/permalink/provcat45641
Yolanda N. Evans, Alicia Dixon Docter, editors. --Cham: Springer , c2020.
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Adolescents have unique nutritional needs when compared to young children and adults. As youth go through physical, cognitive, and behavioral development, nutrition needs are dynamic and changing. If these needs go undetected and remain unaddressed, the results can derail physical and social maturation and include life-long effects on health. This comprehensive text offers a multidisciplinary perspective on aspects of adolescent nutrition. Using clinical cases, it covers relevant topics related…
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Other Authors
Evans, Yolanda N.
Dixon Docter, Alicia
Responsibility
Yolanda N. Evans, Alicia Dixon Docter, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2020
Physical Description
1 online resource (xvi, 839 p.) : 42 illus., 25 illus. in color
ISBN
9783030451035
9783030451028 (Print ed.)
9783030451042 (Print ed.)
Subjects (MeSH)
Adolescent Health
Feeding and Eating Disorders
Nutrition Disorders
Nutritional Physiological Phenomena
Specialty
Adolescent Medicine
Nutrition Therapy
Nutritional Sciences
Abstract
Adolescents have unique nutritional needs when compared to young children and adults. As youth go through physical, cognitive, and behavioral development, nutrition needs are dynamic and changing. If these needs go undetected and remain unaddressed, the results can derail physical and social maturation and include life-long effects on health. This comprehensive text offers a multidisciplinary perspective on aspects of adolescent nutrition. Using clinical cases, it covers relevant topics related to adolescent health including normal development, chronic health conditions, and complex biopsychosocial dynamics, among others. The first section of the text contains an overview of adolescent nutrition that is further broken down into more specific topics such as developmental nutrition needs, needs of active youth and athletes and media influences on body image. The next section focuses on health disparities such as culturally appropriate care, health equity, international considerations and food insecurity. The following section specifically addresses eating disorders ranging from anorexia and bulimia to binge eating. Finally, the last section covers additional health considerations such as polycystic ovarian syndrome, teen pregnancy, substance use and gender non-conforming youth. Written by experts in the field, this book is a helpful resource for primary care medical providers, registered dietitians, adolescent medicine specialists as well as advanced practice nurses, physician assistants and athletic trainers.
Contents
Part I. General Adolescent Nutrition -- 1. General Adolescent Development -- 2. Confidentiality -- 3. Communication and Adolescents -- 4. Developmental Nutrition -- 5. Wellness and Excessive Weight Gain -- 6. Ensuring Nutritional Adequacy in the Adolescent and Young Adult Athlete -- 7. Media Influences on Body Image & Eating Behaviors in Adolescents -- Part II. Caring for Diverse Populations -- 8. Supporting & Promoting Adolescent Nutritional Health Equity -- 9. Food Insecurity Among Adolescents and Emerging Adults -- 10. Culturally Appropriate Care -- 11. International Considerations -- 12. Health at Every Size® -- 13. Juvenile Justice -- Part III. Disordered Eating -- 14. Anorexia Nervosa -- 15. Bulimia Nervosa -- 16. Avoidant/Restrictive Food Intake Disorder (ARFID) -- 17. Binge Eating Disorder in Adolescents and Emerging Adults -- 18. Otherwise Specified and Unspecified Feeding or Eating Disorders -- 19. Co-occurring Eating Disorders and Type 1 Diabetes Mellitus -- 20. Co-Occurring Eating Disorders and Orthorexia Nervosa -- Part IV. Additional Health Considerations -- 21. Polycystic Ovarian Syndrome (PCOS) -- 22. Type 1 Diabetes Mellitus -- 23. Type II Diabetes Mellitus -- 24. Nutrition in Adolescent Pregnancy -- 25. Adolescent Substance Use -- 26. Nurturing Healthy Transitions: Nutrition, Exercise, and Body Image for Transgender and Gender Diverse Youth.
Format
e-Book
Location
Online
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Androgen Excess Disorders in Women : Polycystic Ovary Syndrome and Other Disorders

https://libcat.nshealth.ca/en/permalink/provcat29185
edited by Ricardo Azziz, John E. Nestler, Didier Dewailly. (2nd ed.) --Totowa, NJ: Humana Press , c2007.
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Online
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Author
Azziz, Ricardo
Other Authors
Nestler, John E
Dewailly, Didier
Responsibility
edited by Ricardo Azziz, John E. Nestler, Didier Dewailly
Edition
2nd ed.
Place of Publication
Totowa, NJ
Publisher
Humana Press
Date of Publication
c2007
Series Title
Contemporary endocrinology (Totowa, N.J.)
ISBN
9781597451796
Subjects (MeSH)
Adrenocortical hyperfunction
Androgens
Hyperandrogenism
Polycystic Ovary Syndrome
Subjects (LCSH)
Endocrinology 
Gynecology
Format
e-Book
Location
Online
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Atlas of Genetic Diagnosis and Counseling

https://libcat.nshealth.ca/en/permalink/provcat41222
Harold Chen. (Third edition) --New York, NY: Springer , 2017.
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Dr. Harold Chen shares his almost 50 years of clinical genetics practice in this new edition of a comprehensive pictorial atlas, featuring almost 290 genetic disorders, malformations, and malformation syndromes. The author provides a detailed outline for each disorder, describing its genetics, basic defects, clinical features, diagnostic tests, and counseling issues, including recurrence risk, prenatal diagnosis, and management. Numerous color photographs of prenatal ultrasounds, imagings, cyto…
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Author
Chen, Harold
Responsibility
Harold Chen
Edition
Third edition
Place of Publication
New York, NY
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xxiii, 3080 pages) : 1242 illus., 1050 illus. in color
Series Title
Springer reference
ISBN
9781493924011
9781493924004 (print ed.)
Subjects (MeSH)
Genetic Counseling
Genetic Diseases, Inborn
Prenatal Diagnosis
Abstract
Dr. Harold Chen shares his almost 50 years of clinical genetics practice in this new edition of a comprehensive pictorial atlas, featuring almost 290 genetic disorders, malformations, and malformation syndromes. The author provides a detailed outline for each disorder, describing its genetics, basic defects, clinical features, diagnostic tests, and counseling issues, including recurrence risk, prenatal diagnosis, and management. Numerous color photographs of prenatal ultrasounds, imagings, cytogenetics, and postmortem findings illustrate the clinical features of patients at different ages, patients with varying degrees of severity, and the optimal diagnostic strategies. The disorders cited are supplemented by case histories and diagnostic confirmation by cytogenetics, biochemical, and molecular techniques, when available. Since the publication of the previous edition in 2012, the atlas has been widely accepted and used in light of rapid progress in genetic and gnomic information. In this new edition, additional genetic disorders are added, as well as extensive updates to the previous disorders with new illustrations, supplemented by case and family history, clinical features, and laboratory data, especially molecular confirmation if available. The atlas is written in outline format for ease of use. Atlas of Genetic Diagnosis and Counseling, Third Edition is of great value to medical geneticists, genetic counselors, pediatricians, neonatologists, developmental pediatricians, perinatologists, obstetricians, neurologists, pathologists, and any physicians and health care professionals caring for handicapped children such as craniofacial surgeons, plastic surgeons, otolaryngologists, and orthopedists. It is the definitive volume for helping all physicians to understand and recognize genetic diseases and malformation syndrom es and better evaluate, counsel, and manage affected patients.
Contents
Acardia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver Syndrome -- Agnathia -- Aicardi Syndrome -- Alagille Syndrome -- Albinism -- Alpha-Thalassemia X-linked Mental Retardation Syndrome -- Ambiguous Genitalia -- Amniotic Deformity, Adhesions, Mutilations (ADAM) Complex -- Androgen Insensitivity Syndrome -- Angelman Syndrome -- Apert Syndrome -- Aplasia Cutis Congenita -- Arthrogryposis Multiplex Congenita -- Asphyxiating Thoracic Dystrophy -- Ataxia-Telangiectasia -- Atelosteogenesis -- Autism -- Bannayan-Riley-Ruvalcaba Syndrome -- Beckwith-Wiedemann Syndrome -- Behcet Disease -- Biotinidase Deficiency -- Bladder Exstrophy -- Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome -- Body Stalk Anomaly -- Brachydactyly -- Branchial Cleft Anomalies -- Calcinosis Cutis -- Campomelic Dysplasia -- Carpenter Syndrome -- Cat Eye Syndrome -- Celiac Disease -- Cerebral Palsy -- Cerebro-Costo-Mandibular Syndrome -- Charcot-Marie-Tooth Disease -- CHARGE Syndrome -- Cherubism -- Chiari Malformation -- Chondrodysplasia Punctata -- Chromosome Abnormalities in Pediatric Solid Tumors -- Cleft Lip and/or Cleft Palate -- Cleidocranial Dysplasia -- Cloacal Exstrophy -- Clubfoot -- Collodion Baby -- Congenital Adrenal Hyperplasia -- Congenital Cutis Laxa -- Congenital Cytomegalovirus Infection -- Congenital Generalized Lipodystrophy -- Congenital Hemihyperplasia -- Congenital Hydrocephalus -- Congenital Hypothyroidism -- Congenital Muscular Dystrophy -- Congenital Toxoplasmosis -- Conjoined Twins -- Corpus Callosum Agenesis/Dysgenesis -- Craniometaphyseal Dysplasia -- Cri-Du-Chat Syndrome -- Crouzon Syndrome -- Cutaneous Vasculitis -- Cutis Marmorata Telangiectatica Congenita -- Cystic Fibrosis -- Dandy-Walker Malformation -- De Lange Syndrome -- Del(18p) Syndrome -- Del(22q11.2) Syndrome -- Del(Yq) Syndrome -- Diabetic Embryopathy -- Down Syndrome -- Duncan Syndrome -- Dyschondrosteosis -- Dysmelia -- Dysplasia Epiphysealis Hemimelica -- Dystonia -- Dystrophinopathies -- Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome -- Ehlers-Danlos Syndrome -- Ellis-van Creveld Syndrome -- Enchondromatosis -- Epidermolysis Bullosa -- Epidermolytic Palmoplantar Keratoderma -- Faciogenital (Faciodigitogenital) Dysplasia -- Facioscapulohumeral Muscular Dystrophy -- Familial Adenomatous Polyposis -- Familial Hyperlysinemia -- Familial Mediterranean Fever -- Familial Patella Instability -- Familial Spastic Paraplegia -- Fanconi Anemia -- Feingold Syndrome -- Femoral Hypoplasia - Unusual Facies Syndrome -- Fetal Akinesia Deformation Sequence -- Fetal Alcohol Spectrum Disorders -- Fetal Hydantoin Syndrome -- Fibrodysplasia Ossificans Progressiva -- Fibular Hemimelia -- Finlay-Marks Syndrome -- Floppy Infant -- Fragile X Syndrome -- Fraser Syndrome -- Freeman-Sheldon Syndrome -- Friedreich Ataxia -- Frontonasal Dysplasia -- Galactosemia -- Gastroschisis -- Gaucher Disease -- Generalized Arterial Calcification of Infancy -- Genitopatellar Syndrome -- Giant Congenital Melanocytic Nevi -- Gilbert Syndrome -- Glucose-6-Phosphate Dehydrogenase Deficiency -- Glycogen Storage Disease, Type 2 -- Goldenhar Syndrome -- Gorlin Syndrome -- Greig Cephalopolysyndactyly Syndrome -- Growth Hormone Deficiency -- Hallermann-Streiff Syndrome -- Harlequin Ichthyosis -- Hemangiomas of Infancy -- Hemophilia A -- Hereditary Hearing Loss -- Hereditary -- Hemochromatosis -- Hereditary Multiple Exostoses -- Hereditary Sensory and Autonomic Neuropathies -- Herlyn-Werner-Wunderlich Syndrome -- Holoprosencephaly -- Holt-Oram Syndrome -- Huntington Disease -- Hydranencephaly -- Hydrolethalus Syndrome -- Hydrops Fetalis -- Hyper-IgE Syndrome -- Hypertrophic Cardiomyopathy (HCM) -- Hypochondroplasia -- Hypoglossia-Hypodactylia Syndrome -- Hypohidrotic Ectodermal Dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Hypopituitarism -- I(1p), I(1q) Syndrome -- Idic(Yq) Syndrome -- Incontinentia Pigmenti -- Infantile Myofibromatosis -- Ivemark Syndrome -- Jarcho-Levin Syndrome -- Joubert Syndrome -- Kabuki Syndrome -- Kasabach-Merritt Syndrome -- KID Syndrome -- Klinefelter Syndrome -- Klippel-Feil Syndrome -- Klippel-Trenaunay Syndrome -- Kniest Dysplasia -- Larsen Syndrome -- LEOPARD Syndrome -- Lesch-Nyhan Syndrome -- Lethal Multiple Pterygium Syndrome -- Loeys-Dietz Syndrome -- Lowe Syndrome -- Lymphangiomas and Lymphangiomatosis -- M#xf6;bius Syndrome -- Macrodactyly -- Marfan Syndrome -- McCune-Albright Syndrome -- Meckel-Gruber Syndrome -- Megalencephalic Leukoencephalopathy with Subcortical Cysts -- Menkes Disease -- Metachromatic Leukodystrophy -- Miller-Dieker Syndrome -- Mitochondrial Leber Hereditary Optic Neuropathy -- Mitochondrial Myopathy -- Mowat-Wilson Syndrome -- Mucolipidosis 2 -- Mucolipidosis 3 -- Mucopolysaccharidosis 1 (MPS 1) -- Mucopolysaccharidosis 2 -- Mucopolysaccharidosis 3 -- Mucopolysaccharidosis 4 -- Mucopolysaccharidosis 6 -- Multiple Endocrine Neoplasia Syndromes -- Multiple Epiphyseal Dysplasia -- Multiple Pterygium Syndrome -- Myotonic Dystrophy Type 1 -- Nager Acrofacial Dysostosis -- Nail-Patella Syndrome -- Nasal Obstruction in Neonates and Children -- Neonatal Herpes Simplex Infection -- Nephrogenic Diabetes Insipidus -- Netherton Syndrome -- Neu-Laxova Syndrome -- Neural Tube Defects -- Neurofibromatosis 1 -- Neurofibromatosis 2 -- Niemann-Pick Disease -- Noonan Syndrome -- Oblique Facial Cleft Syndrome -- Oligohydramnios Sequence -- Omphalocele -- Opitz Trigonocephaly (C) Syndrome -- Oral-Facial-Digital Syndrome -- Osteogenesis Imperfecta -- Osteogenesis Imperfecta Ehlers-Danlos Overlap Syndrome -- Osteopetrosis -- Osteopoikilosis -- Otopalatodigital Spectrum Disorders -- Pachyonychia Congenita -- Pallister-Killian Syndrome -- Peutz-Jeghers Syndrome -- Phenylketonuria -- Pierre Robin Sequence -- Polycystic Kidney Disease, Autosomal Dominant Type -- Polycystic Kidney Disease: Autosomal Recessive Type -- Popliteal Pterygium Syndrome -- Prader-Willi Syndrome -- Primary Microcephaly -- Progeria -- Prune Belly Syndrome -- Pseudoachondroplasia -- R(18) Syndrome -- Radioulnar Synostosis -- Retinoid Embryopathy -- Rett Syndrome -- Rickets -- Rigid Spine Syndrome -- Roberts Syndrome -- Robinow Syndrome -- Rubinstein-Taybi Syndrome -- Saethre-Chotzen Syndrome -- Sagittal Craniosynostosis Associated with Chromosome Abnormalities with a Brief Review on Craniosynostosis -- Schizencephaly Schmid Metaphyseal Chondrodysplasia -- Seckel Syndrome -- Severe Combined Immune Deficiency -- Short Rib-Polydactyly Syndromes -- Sickle Cell Disease -- Silver-Russell Syndrome -- Sirenomelia -- Smith-Lemli-Opitz Syndrome -- Smith-Magenis Syndrome -- Sotos Syndrome -- Spinal Muscular Atrophy -- Spondyloepiphyseal Dysplasia -- Stickler Syndrome -- Sturge-Webber Syndrome -- Symphalangism -- Tay-Sachs Disease -- Tetrasomy 9p Syndrome -- Thalassemia -- Thanatophoric Dysplasia -- Thrombocytopenia-Absent Radius Syndrome -- Treacher-Collins Syndrome -- Trimethylaminuria -- Triploidy -- Trismus-Pseudocamptodactyly Syndrome -- Trisomy 13 Syndrome -- Trisomy 18 Syndrome -- Trisomy 8 Mosaicism Syndrome -- Tuberous Sclerosis -- Turner Syndrome -- Twin-Twin Transfusion Syndrome -- Tyrosinemia -- Ulnar-Mammary Syndrome -- Urofacial Syndrome -- VATER (VACTERL) Association -- Von Hippel-Lindau Disease -- Waardenburg Syndrome -- Weill-Marchesani Syndrome -- Williams Syndrome -- Winchester syndrome -- Wolf-Hirschhorn Syndrome -- X-Linked Agammaglobulinemia -- X-Linked Ichthyosis -- XX Male -- XXX Syndrome -- XXXXX Syndrome -- XXXXY Syndrome -- XY Female -- XYY Syndrome.
Format
e-Book
Publication Type
Encyclopedia
Location
Online
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Atlas of Imaging in Infertility : A Complete Guide Based in Key Images

https://libcat.nshealth.ca/en/permalink/provcat41252
Luis Ronan Marquez Ferreira de Souza, Ana Luisa Alencar De Nicola, Harley De Nicola, editors. --Cham: Springer , 2017.
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This atlas gathers the most frequent imaging findings concerning alterations that cause infertility in both males and in females. Also, it discusses how the images should be analyzed and described, to serve as a guide for the physicians who request and perform these imaging tests. Infertility is a highly prevalent condition: about 10% of couples are infertile with males and females equally affected. This book offers professionals dealing with infertility, including endocrinologists, gynecologis…
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Other Authors
de Souza, Luis Ronan Marquez Ferreira
De Nicola, Ana Luisa Alencar
De Nicola, Harley
Responsibility
Luis Ronan Marquez Ferreira de Souza, Ana Luisa Alencar De Nicola, Harley De Nicola, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xii, 214 pages) : 298 illus., 193 illus. in color
ISBN
9783319138930
9783319138923 (print ed.)
Subjects (MeSH)
Infertility, Female - diagnostic imaging
Infertility, Male - diagnostic imaging
Abstract
This atlas gathers the most frequent imaging findings concerning alterations that cause infertility in both males and in females. Also, it discusses how the images should be analyzed and described, to serve as a guide for the physicians who request and perform these imaging tests. Infertility is a highly prevalent condition: about 10% of couples are infertile with males and females equally affected. This book offers professionals dealing with infertility, including endocrinologists, gynecologists and urologists, a useful guide to the diagnostic imaging tests that are essential in treating these patients. The Atlas of Imaging in Infertility is a valuable resource for physicians from different specialties managing cases of infertility.
Contents
1. Anatomy and Embryology -- Part I: Imaging of Female Infertility -- 2 Polycystic Ovarian Syndrome -- 3. Tubal Diseases -- 4. Pelvic Inflammatory Disease -- 5. Endometriosis -- 6. Leiomyoma and Cavitary Lesions -- 7. Adenomyosis -- 8. Müllerian Duct Anomalies -- Part II: Imaging of Male Infertility -- 9. Obstructive Disorders -- 10. Non-obstructive Diseases of the Testes -- Part III: Other Diseases -- 11. The Sella Turcica -- 12. Adrenal Gland Diseases.
Format
e-Book
Publication Type
Atlas
Location
Online
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Atlas of the Mammalian Ovary : Morphological Dynamics and Potential Role of Innate Immunity

https://libcat.nshealth.ca/en/permalink/provcat31189
Katharina Spanel-Borowski. --Berlin, Heidelberg: Springer , c2012.
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In the era of molecular biology, an atlas that allows a rapid understanding of the complexity of ovarian processes is urgently needed. In this book, the author draws upon her own research, conducted over the past three decades, to provide a unique compilation of high-quality illustrations that offer illuminating insights in a readily accessible form. The ovarian follicles, the corpus luteum, and the interstitial cortex are presented as precisely controlled homeostatic compartments. Physiologic …
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Author
Spanel-Borowski, Katharina
Responsibility
Katharina Spanel-Borowski
Place of Publication
Berlin, Heidelberg
Publisher
Springer
Date of Publication
c2012
Physical Description
1 online resource (xiv, 141 p. : 78 ill., 58 ill. in color)
ISBN
9783642305351
Subjects (MeSH)
Immunity, Innate
Ovary - anatomy & histology - Atlases
Ovary - immunology
Subjects (LCSH)
Anatomy
Immunology
Gynecology
Endocrinology 
Reproductive medicine
Abstract
In the era of molecular biology, an atlas that allows a rapid understanding of the complexity of ovarian processes is urgently needed. In this book, the author draws upon her own research, conducted over the past three decades, to provide a unique compilation of high-quality illustrations that offer illuminating insights in a readily accessible form. The ovarian follicles, the corpus luteum, and the interstitial cortex are presented as precisely controlled homeostatic compartments. Physiologic cell death forms and leukocyte subtypes are clearly depicted, and the various steps in the ovulatory process are demonstrated in detail. Further topics addressed include the microvascular bed, the plasticity of intraovarian nerves as part of the remodelling processes in the polycystic and the menopausal ovary, and the role of cytokeratin-positive cells (of steroidogenic or microvascular origin) as messengers of innate immunity. This atlas will be a fascinating and informative resource for both trainees and more experienced professionals.
Contents
Introduction -- Follicle stages and follicular atresia without and with irradiation -- Follicular atresia as proliferative and inflammatory event -- Cortex and cellular stromolysis -- The ovulatory period as acute inflammatory response to oxidative stress and follicle cell harvest -- Corpus luteum cycle with focus on capillary sprouting and regression, eosinophils and KIT-positive cells -- Intraovarian oocyte release (IOR) with severe tissue damage -- Vascular stromolysis and vascular luteolysis for bulk tissue removal -- Polycystic and postmenopausal ovaries and negligible mast cells -- Cytokeratin-positive cells as dendritic-like cells and potential albumin-coexpression in follicles and corpus luteum -- Aspects of immunological control, novel concepts, challenges and clinical perspectives.
Format
e-Book
Location
Online
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Bariatric Surgical Practice Guide : Recommendations

https://libcat.nshealth.ca/en/permalink/provcat41963
Saravana Kumar, Rachel Maria Gomes, editors. --Singapore: Springer , 2017.
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This book provides a comprehensive review of literature of various aspects of bariatric surgery arriving at practical recommendations for simplifying day to day practice. This book is divided into 10 sections covering selection of patient, preoperative predictors of outcome, technical considerations, specific situations, post-operative pathways, management of complications, revisional surgery, and perioperative nutritional aspects. It covers specific situations in bariatric surgery such as GERD…
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Other Authors
Kumar, Saravana
Gomes, Rachel Maria
Responsibility
Saravana Kumar, Rachel Maria Gomes, editors
Place of Publication
Singapore
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xviii, 309 pages) : 1 illus.
ISBN
9789811027055
9789811027048 (print ed.)
Subjects (MeSH)
Bariatric Surgery - methods
Intraoperative Complications - prevention & control
Nutritional Physiological Phenomena
Obesity - surgery
Patient Selection
Postoperative Complications - prevention & control
Abstract
This book provides a comprehensive review of literature of various aspects of bariatric surgery arriving at practical recommendations for simplifying day to day practice. This book is divided into 10 sections covering selection of patient, preoperative predictors of outcome, technical considerations, specific situations, post-operative pathways, management of complications, revisional surgery, and perioperative nutritional aspects. It covers specific situations in bariatric surgery such as GERD, hernia repair, gallstone disease, PCOD, NAFLD and end-organ disease. Bariatric Surgical Practice Guide is a quick resource for practicing bariatric surgeons, young and experienced, to understand all practical aspects of this surgery which is gaining importance worldwide at a rapid pace. Recommendations are based on existing literature as well as opinions of the authors who work at state-of-the-art clinical facilities.
Contents
Part I. Selection of a patient -- 1. Selection guidelines for bariatric surgery -- 2. Bariatric surgery in adolescents -- 3. Selection of bariatric surgery procedures in special circumstances -- 4. Preoperative evaluation and contraindications to bariatric surgery -- Part II. Preoperative predictors of outcomes -- 5. Definition of outcomes after bariatric surgery -- 6. Preoperative predictors of weightloss after bariatric surgery -- 7. Preoperative predictors of Diabetes control following bariatric surgery -- Part III. Technical considerations -- 8. Standardization of technique in sleeve gastrectomy -- 9. Technical considerations in gastric plication with or without a band -- 10. Standardization of technique in roux-en-Y gastric bypass -- 11. Technical considerations of duodenal switch and variants -- Part IV: Specific situations in bariatric surgery -- 12. Gastroesophageal reflux disease and bariatric surgery -- 13. Ventral hernia repair in the morbidly obese -- 14. Gallstone disease before and after bariatric surgery -- 15. Polycystic ovarian disease, pregnancy and bariatric surgery -- 16. Nonalcoholic fatty liver disease and effects of bariatric surgery -- 17. Outcomes of diabetic microvascular complications after bariatric surgery -- 18. Role of bariatric surgery in end-organ failure -- Part V: Postoperative pathways -- 19. Peri-operative venous thromboembolism prophylaxis after bariatric surgery -- 20. Peri-operative management of medical comorbidities after bariatric surgery -- 21. Peri-operative management of obstructive sleep apnea after bariatric surgery -- 22. Enhanced recovery after bariatric surgery -- Part VI: Surgical complications after bariatric surgery -- 23. Post Sleeve gastrectomy leaks -- 24. Detection and management of internal hernias -- 25. Prevention and management of marginal ulcers -- 26. Prevention and management of gastro-jejunostomy strictures -- 27. Management of leaks after gastric bypass -- 28. Prevention and management of bleeding after sleeve gastrectomy and gastric bypass -- Part VII: Revisional bariatric surgery -- 29. Revisional surgical options after laparoscopic adjustable gastric banding -- 30. Revisional surgical options after laparoscopic sleeve gastrectomy -- 31. Revisional surgical options after laparoscopic roux-en-Y gastric bypass -- Part VIII: Nutritional management in bariatric surgery -- 32. Perioperative diet management in bariatric surgery -- 33. Importance of proteins after bariatric surgery -- 34. Anaemia and related deficiencies in bariatric surgery -- 35. Calcium and vitamin D deficiencies in bariatric surgery -- 36. Other micronutrient deficiencies in bariatric surgery.
Format
e-Book
Location
Online
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Benign Tumors of the Liver

https://libcat.nshealth.ca/en/permalink/provcat39151
Luca Aldrighetti, Francesco Cetta, Gianfranco Ferla, editors. --Cham: Springer , c2015.
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Diagnosis of benign tumors of the liver is experiencing exponential growth, mainly owing to the diffusion of more accurate imaging techniques. This monograph opens by examining the epidemiology, histopathology, and genetics of these diseases and discussing liver physiopathology. The role of imaging techniques is described, and clear guidance provided on differential diagnosis. The full range of benign liver tumors and conditions is then systematically reviewed, including liver cysts and polycys…
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Other Authors
Aldrighetti, Luca
Cetta, Francesco
Ferla, Gianfranco
Responsibility
Luca Aldrighetti, Francesco Cetta, Gianfranco Ferla, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2015
Physical Description
1 online resource (xvi, 337 p. : 110 illus., 57 illus. in color)
ISBN
9783319129853
9783319129846 (print ed.)
Subjects (MeSH)
Liver Neoplasms - diagnosis
Liver Neoplasms - therapy
Liver - physiopathology
Abstract
Diagnosis of benign tumors of the liver is experiencing exponential growth, mainly owing to the diffusion of more accurate imaging techniques. This monograph opens by examining the epidemiology, histopathology, and genetics of these diseases and discussing liver physiopathology. The role of imaging techniques is described, and clear guidance provided on differential diagnosis. The full range of benign liver tumors and conditions is then systematically reviewed, including liver cysts and polycystic liver disease, Caroli disease, hemangiomas, focal nodular hyperplasia, adenomas, hepatic manifestations of systemic diseases, and focal infectious diseases. Surgical indications are accurately analyzed, with a view to assisting in the avoidance of useless interventions. Transplantation, laparoscopic resection, and robotic surgical techniques are described and illustrated, emphasizing the optimization of intra- and postoperative management in order to avoid potential complications and degeneration. In these chapters, attention is drawn to the ways in which the surgical management of benign liver tumors differs from that of malignant tumors. Information is also provided on anesthesia, blood transfusion, the role of interventional radiology in patients with benign liver tumors and fast track programs for liver surgery. This book, in handy format, will prove essential reading for all who are interested in benign liver surgery and will represent an invaluable source of knowledge for general and hepatobiliary surgeons, whether in training or practice.
Contents
Foreword -- Preface -- Part I: General Perspective -- 1. Epidemiology and Histopathology of Benign Liver Tumors -- 2. Molecular Biology and Genetics of Benign Liver Tumors -- 3. Genetic Syndromes and Benign Liver Tumors (Multiple Adenomas in Glycogen Storage Disease) -- 4. Liver Physiopathology (Ischemia/Reperfusion, Factors affecting Liver Regeneration) -- Part II: Imaging -- 5. Imaging Techniques (Ultrasound, CT, MR) of Benign Liver Tumors -- 6. Imaging Morphology in Benign Liver Tumors -- 7. Differential Diagnosis of Benign Liver Tumors -- Part III: Systematic Review of Benign Liver Tumors -- 8. Cysts and Polycystic Liver Disease -- 9. Caroli's Disease: Cystic Bile Duct Dilatations -- 10.Hepatolithiasis -- 11. Hemangiomas -- 12. Focal Nodular Hyperplasia -- 13. Hepatocellular Adenoma -- 14. Adenoma and Biliary Cystadenoma -- 15.Benign Tumors of Bile Ducts and Gallbladder -- 16. Liver Focal Localizations of Systemic Diseases -- 17. Focal Infectious Diseases -- Part IV: Treatment of Benign Liver Tumors -- 18. Transplantation for Benign Liver Lesions -- 19. Laparoscopic Liver Surgery in Benign Liver Lesions -- 20. Robotic Liver Resection for Benign Tumors -- 21. Interventional Radiology in Benign Liver Tumors: Embolization and Ablation -- 22. Intraoperative Ultrasound in Liver Surgery for Benign Tumors -- 23. Anesthesia and Intraoperative Management in Liver Surgery -- 24. Blood and Transfusion Management in Benign Liver Tumors -- 25. Fast Track Programs in Benign Liver Tumors.
Format
e-Book
Location
Online
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Cancer of the ovary

https://libcat.nshealth.ca/en/permalink/provcat27283
[edited by] Rodney Reznek. --Cambridge, UK: Cambridge University Press , 2007.
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Location
Online
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Author
Reznek, Rodney H
Responsibility
[edited by] Rodney Reznek
Place of Publication
Cambridge, UK
Publisher
Cambridge University Press
Date of Publication
2007
Physical Description
176 p.
Series Title
Contemporary issues in cancer imaging
ISBN
6610749310
Subjects (MeSH)
Ovarian Neoplasms
Contents
Cover -- Half-title -- Series-title -- Title -- Copyright -- Contents -- Contributors -- Series Foreword -- Preface to Cancer of the Ovary -- 1 Epidemiology of Ovarian Cancer -- Introduction -- Genetic Epidemiology -- Familial Risks -- Genetic Susceptibility to Ovarian Cancer -- Low Penetrance Ovarian Cancer Susceptibility -- Reproductive and Hormonal Factors -- Early Menarche and Late Menopause -- Parity -- Lactation -- Oral Contraceptive Pill -- Infertility -- Hormone Replacement Therapy -- Other Factors -- Age -- Talcum Powder -- Pelvic Surgery -- Endometriosis -- Polycystic Ovarian Syndrome (PCOS) -- Pelvic Inflammatory Disease (PID) -- Diet -- Conclusion -- REFERENCES -- 2 The Pathological Features of Ovarian Neoplasia -- Introduction -- Non-Neoplastic Cysts -- Ovarian Neoplasms -- Benign Epithelial and Mixed Ovarian Tumours -- Serous Cystadenoma -- Mucinous Cystadenoma -- Endometrioid Cystadenoma -- Brenner Tumour -- Borderline Epithelial Ovarian Tumours -- Borderline Serous Ovarian Neoplasia -- Borderline Mucinous Ovarian Neoplasia -- Borderline Endometrioid Ovarian Neoplasia -- Borderline Ovarian Brenner Tumour -- Invasive Epithelial Ovarian Tumours -- Serous Ovarian Carcinoma -- Mucinous Ovarian Carcinoma -- Endometrioid Ovarian Carcinoma -- Malignant Brenner and Transitional Cell Ovarian Carcinoma -- Germ Cell Tumours of the Ovary -- Dysgerminoma -- Yolk Sac Tumour -- Sex Cord and Stromal Tumours of the Ovary -- Granulosa Cell Tumours -- Thecoma and Fibroma -- Sertoli-Leydig Cell Tumours -- Staging of Ovarian Neoplasms -- Tumours Metastatic to the Ovary -- Conclusion -- REFERENCES -- 3 Ovarian Cancer Screening -- Introduction -- Screening Test Requirements -- Screening Techniques -- Vaginal Examination -- Tumour Markers -- Ultrasound -- Other Modalities -- Multimodal Screening -- Test Acceptability -- Target Populations -- The 'High-Risk' Population -- The General Population -- The Cost of Screening -- Conclusions -- Acknowledgement -- REFERENCES -- 4 Surgical Management of Patients with Epithelial Ovarian Cancer -- Introduction -- Staging Laparotomy -- Primary Cytoreductive Surgery -- Delayed Primary Surgery following Neoadjuvant Chemotherapy -- Interval Debulking following Induction Chemotherapy -- Cytoreductive Surgery for Recurrent Ovarian Cancer -- Palliative Surgery for Recurrent Ovarian Cancer -- Conclusion -- REFERENCES -- 5 Medical Treatment of Ovarian Carcinoma -- Introduction -- Chemotherapy in Early Stage Disease -- Chemotherapy in Advanced Disease -- Systemic Chemotherapy -- Other Treatment Approaches -- Relapsed Ovarian Cancer -- Chemotherapy -- Other Platinum Agents -- Combination versus Single-Agent Therapy -- Response Prediction -- When should Treatment be Started? -- Other Treatment Approaches -- Endocrine Therapies -- Conclusion -- REFERENCES -- 6 Ultrasound in Ovarian Carcinoma -- Ultrasonic Technique -- Morphological Assessment -- Doppler Examination -- New Developments -- Ultrasonic Diagnosis of Malignancy -- Malignant Features -- Ultrasonic Features of Primary Malignancies -- Differential Diagnosis of Adnexal Masses -- Simple Ovarian Cysts --T$74
Format
e-Book
Location
Online
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A Case-Based Guide to Clinical Endocrinology

https://libcat.nshealth.ca/en/permalink/provcat39002
Terry F. Davies, editor. (Second edition) --New York, NY: Springer , c2015.
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In A Case-Based Guide to Clinical Endocrinology, Second Edition, a renowned group of distinguished clinicians once again provides stimulating instruction and insights into a wide variety of endocrine topics, teaching readers modern management of the conditions described andáoffering targeted entry into the literature. Importantly, many of the important elements in the current curriculum for clinical endocrine training as recommended by the Association of Program Directors in Clinical Endocrinol…
Available Online
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Other Authors
Davies, Terry F
Responsibility
Terry F. Davies, editor
Edition
Second edition
Place of Publication
New York, NY
Publisher
Springer
Date of Publication
c2015
Physical Description
1 online resource (xvii, 453 p. : 31 illus., 18 illus. in color)
ISBN
9781493920594
9781493920587 (print ed.)
Subjects (MeSH)
Endocrine System Diseases
Endocrine System - pathology
Abstract
In A Case-Based Guide to Clinical Endocrinology, Second Edition, a renowned group of distinguished clinicians once again provides stimulating instruction and insights into a wide variety of endocrine topics, teaching readers modern management of the conditions described andáoffering targeted entry into the literature. Importantly, many of the important elements in the current curriculum for clinical endocrine training as recommended by the Association of Program Directors in Clinical Endocrinology, Diabetes and Metabolism are covered in this text. Thoroughly updated, this new edition not only covers new treatment approaches but also emphasizes the latest investigative advances in both imaging and molecular diagnostics. To reinforce learning and retention of knowledge, a question-based approach is used in many of the case studies. Students, residents, fellows, and practitioners will find this reference to be an efficient way to review their understanding and increase their skills and abilities in patient investigation and management. An invaluable contribution to the field, A Case-Based Guide to Clinical Endocrinology, Second Edition, offers the same comprehensive volume of thought-provoking case-studies that made the first edition of significant importance to all clinicians who treat patients with endocrine disorders.
Contents
Part I. Pituitary -- 1 Introduction -- 2 Acromegaly, Awareness Is Paramount for Early Diagnosis: Highlights of Diagnosis and Treatment Challenges -- 3 A Nontraumatic Hip Fracture in a Young Woman: Cushing’s Disease—Consequences of a Late Diagnosis and Treatment Highlights -- 4 Idiopathic Granulomatous Hypophysitis Masquerading as a Pituitary Adenoma: Are There Reliable Diagnostic Criteria? -- Part II. Thyroid Overactivity -- 5 Introduction -- 6 TSH-Secreting Pituitary Adenoma -- 7 Struma Ovarii -- 8 Exogenous Thyrotoxicosis -- Part III. Thyroid Underactivity -- 9 Introduction -- 10 Central Hypothyroidism -- 11 Treatment of Hypothyroidism: Utility of Adding T3 (Liothyronine) -- 12 Hypothyroidism in Pregnancy -- 13 Hypothyroid Myopathy and Thelogen Effluvium -- Part IV. Thyroid Cancer -- 14 Introduction -- 15 Approach to the Patient with an Incidentally Discovered Thyroid Nodule -- 16 Papillary Thyroid Cancer -- 17 Metastatic Papillary Thyroid Cancer -- 18 Management of Metastatic Medullary Thyroid Cancer -- 19 Thyroid Cancer and Bone Metastases -- Part V. Adrenal -- 20 Introduction -- 21 Primary Aldosteronism -- 22 Adrenal Incidentaloma and Subclinical Hypercortisolism -- 23 A Case of Pheochromocytoma -- Part VI. Hyperparathyroidism -- 24 Introduction -- 25 Complex Primary Hyperparathyroidism -- 26 Differential Diagnosis of Hypocalcemia - 27 Management of Hypoparathyroidism -- 28 Osteomalacia and Primary Hyperparathyroidism -- Part VII. Metabolic Bone Diseases -- 29 Introduction -- 30 Multiple Risk Factors for Osteoporosis and Fracture -- 31 Delayed Diagnosis of Osteoporosis -- 32 Misdiagnosis of Atypical Femur Fractures -- Part VIII. Endocrine Disorders of Men -- 33 Introduction -- 34 Congenital Hypogonadotropic Hypogonadism -- 35 Klinefelter Syndrome -- 36 Low Testosterone and the Metabolic Syndrome -- Part IX. Pregnancy -- 37 Introduction -- 38 Getting Pregnant with PCOS -- 39 Thyrotoxicosis in Pregnancy -- 40 Gestational Diabetes -- Part X. Diabetes -- 41 Introduction: Type-2 Diabetes -- 42 Evaluation and Management of the Newly Diagnosed Patient with Type-2 Diabetes -- 43 Transition to Insulin in Patients with Type-2 Diabetes -- 44 Inpatient Management of Type 2 Diabetes -- Part XI. Lipid Abnormalities -- 45 Introduction -- 46 LDL-Apheresis Therapy for Refractory Familial Hypercholesterolemia -- 47 Familial Type III Hyperlipoproteinemia (Familial Dysbetalipoproteinemia) -- 48 Severe Hypertriglyceridemia -- Part XII. Obesity -- 49 Introduction -- 50 Metabolic Syndrome Case -- 51 The Polycystic Ovarian Syndrome (PCOS) -- 52 Bariatric Surgery.
Format
e-Book
Publication Type
Case Reports
Location
Online
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Clinical Companion in Nephrology

https://libcat.nshealth.ca/en/permalink/provcat45411
Jack Fairweather, Mark Findlay, Christopher Isles. (Second edition) --Cham: Springer , c2020.
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Location
Online
The second edition of this educational book provides an updated resource on how best to discuss and manage acute and chronic presentations of renal diseases. All chapters have been reviewed and updated to reflect changes which directly affect clinical practice and new chapters have been added including Dialysis and Poisoning, Urinalysis/Microscopy and Renal Biopsy. Chapters now include information on key clinical trials for management strategies Allowing for concise reading on specific topics t…
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Author
Fairweather, Jack
Other Authors
Findlay, Mark
Isles, Christopher
Responsibility
Jack Fairweather, Mark Findlay, Christopher Isles
Edition
Second edition
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2020
Physical Description
1 online resource (xiii, 356 p.) : 186 illus., 172 illus. in color
ISBN
9783030383206
9783030383190 (Print ed.)
9783030383213 (Print ed.)
9783030383220 (Print ed.)
Subjects (MeSH)
Kidney Diseases
Specialty
Nephrology
Abstract
The second edition of this educational book provides an updated resource on how best to discuss and manage acute and chronic presentations of renal diseases. All chapters have been reviewed and updated to reflect changes which directly affect clinical practice and new chapters have been added including Dialysis and Poisoning, Urinalysis/Microscopy and Renal Biopsy. Chapters now include information on key clinical trials for management strategies Allowing for concise reading on specific topics this book acts as both a quick reference text and study guide. The layout has been designed in a question and answer format in order to promote self-directed learning. Images and diagrams have been further standardized and improved for the new edition and remain a key feature of the book. Clinical Companion in Nephrology, second edition, is an invaluable resource for junior doctors, medical students and renal nurses who encounter renal patients in their daily practice.
Contents
Part I. Physiology and Assessment -- 1. Structure and Function of the Kidney -- 2. Assessment of GFR -- 3. Proteinuria -- 4. Haematuria -- Part II. Disorders of Renal Metabolic Function -- 5. Hyponatraemia -- 6. Hypokalaemia -- 7. Hypocalcaemia and hypercalcaemia -- 8. Hypophosphataemia and hypomagnesaemia -- 9. Acid-base balance -- Part III. Acute Kidney Injury -- 10. Causes of Acute Kidney Injury -- 11. Rhabdomyolysis -- 12. Cardiorenal Failure -- 13. Hepatorenal Syndrome -- 14. HUS/TTP in Adults -- 15. Myeloma and the Kidney -- 16. Investigation, management and outcome of Acute Kidney Injury -- 17. Fluid Management -- 18. Hyperkalaemia -- 19. Rapidly Progressive Glomerulonephritis -- Part IV. Chronic Kidney Disease -- 20. Overview of Chronic Kidney Disease -- 21. Glomerular Disease -- 22. Diabetes -- 23. Renovascular Disease -- 24. Hypertension -- 25. Antihypertensive Drugs -- 26. Polycystic Kidney Diseases -- 27. Anaemia -- 28. Mineral Metabolism -- 29. Nutrition in Renal Disease -- Part V. Miscellaneous Renal -- 30. Gout and the Kidney -- 31. Urinary Tract Infection -- 32. Renal Stone Disease -- 33. Managing Pain in Chronic Kidney Disease -- 34. The Effect of Kidney Disease on Drugs -- 35. The Effect of Drugs on Kidney Disease -- 36. Pregnancy and Renal Disease -- 37. Blood Borne Viruses -- 38. Rarer Renal Diseases -- Part VI. Renal Replacement Therapy -- 39. Haemodialysis -- 40. Peritoneal Dialysis -- 41. Renal Transplantation -- 42. Dialysis and Poisoning -- 43. Hypertension and Fluid Balance in Dialysis Patients -- 44. Tunnelled Dialysis Catheters -- 45. Catheter Related Blood Stream Infection -- 46. The Challenges of Renal Replacement Therapy in the Frail Older Adult -- Part VII. Practical Nephrology -- 47. Urinalysis and Microscopy -- 48. Dialysis Line Insertion -- 49. Renal Biopsy -- 50. Spotting the Glomerulus: Basics in Biopsy Interpretation -- Appendix A: Treatment of Hyponatraemia -- Appendix B: Treatment of Hypokalaemia -- Appendix C: Treatment of Hypocalcaemia -- Appendix D: Treatment of Hypercalcaemia -- Appendix E: Treatment of Hypophosphataemia and Hypomagnesaemia -- Appendix F: Plasma exchange -- Appendix G: Vasculitis Protocol -- Appendix H: Glucose Lowering Drugs and CKD -- Appendix I: Dietary Potassium Advice -- Appendix J: Dietary Phosphate Advice -- Appendix K: Antibiotics for Urinary Tract Infection -- Appendix L: Iron and Erythropoeisis Stimulating Agents -- Appendix M: Phosphate Binders -- Appendix N: Control of Calcium After Parathyroidectomy -- Appendix O: Prescribing for Chronic Pain in CKD -- Appendix P: Optimal Medical Care on Haemodialysis -- Appendix Q: Immediate Management of PD Peritonitis -- Appendix R: Urokinase Protocol for Blocked Tunnelled Lines -- Appendix S: Reference Values.
Format
e-Book
Location
Online
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Clinical Companion in Nephrology

https://libcat.nshealth.ca/en/permalink/provcat39206
Mark Findlay, Christopher Isles. --Cham: Springer , c2015.
Available Online
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Location
Online
Allowing for concise reading on specific Nephrology topics, this book acts as both a quick reference text and study guide. The authors have designed the layout in a question and answer format in order to stimulate interactive teaching whilst help retain the reader's attention. Clinical Companion in Nephrology is an invaluable resource for medical students, junior doctors and renal nurses. It presents a balance of practical everyday nephrology with a user friendly layout, promoting self-directed…
Available Online
View e-Book
Author
Findlay, Mark
Other Authors
Isles, Christopher
Responsibility
Mark Findlay, Christopher Isles
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2015
Physical Description
1 online resource (xi, 266 p. : 118 illus., 108 illus. in color)
ISBN
9783319148687
9783319148670 (print ed.)
Subjects (MeSH)
Kidney Diseases
Abstract
Allowing for concise reading on specific Nephrology topics, this book acts as both a quick reference text and study guide. The authors have designed the layout in a question and answer format in order to stimulate interactive teaching whilst help retain the reader's attention. Clinical Companion in Nephrology is an invaluable resource for medical students, junior doctors and renal nurses. It presents a balance of practical everyday nephrology with a user friendly layout, promoting self-directed learning.
Contents
Part 1. Physiology and Assessment -- 1. Structure and Function of the Kidney -- 2. Assessment of GFR -- 3. Proteinuria -- 4. Haematuria -- Part 2. Disorders of Renal Metabolic Function -- 5. Hyponatraemia -- 6. Hypokalaemia -- 7. Hypocalcaemia and hypercalcaemia -- 8. Hypophosphataemia and hypomagnesaemia -- 9. Acid-base balance -- Part 3. Acute Kidney Injury -- 10. Causes of Acute Kidney Injury -- 11. Rhabdomyolysis -- 12. Cardiorenal Failure -- 13. Hepatorenal Syndrome -- 14. HUS/TTP in Adults -- 15. Myeloma and the Kidney -- 16. Investigation, management and outcome of Acute Kidney Injury -- 17. Fluid Management -- 18. Hyperkalaemia -- 19. Rapidly Progressive Glomerulonephritis -- Part 4. Chronic Kidney Disease -- 20. Overview of Chronic Kidney Disease -- 21. Glomerular Disease -- 22. Diabetes -- 23. Renovascular Disease -- 24. Hypertension -- 25. Antihypertensive Drugs -- 26. Polycystic Kidney Diseases -- 27. Anaemia -- 28. Mineral Metabolism -- 29. Nutrition in Renal Disease -- Part 5. Miscellaneous Renal -- 30. Gout and the Kidney -- 31. Urinary Tract Infection -- 32. Renal Stone Disease -- 33. Management of Pain -- 34. Pregnancy and Renal Disease -- 35. Blood Borne Viruses -- 36. Rarer Renal Diseases. Part 6. Renal Replacement Therapy -- 37. Haemodialysis -- 38. Peritoneal Dialysis -- 39. Renal Transplantation -- 40. Hypertension and Fluid Balance in Dialysis Patients -- 41. Tunnelled Dialysis Catheters -- 42. Catheter Related Blood Stream Infection -- 43. The Challenges of Renal Replacement Therapy in the Elderly.
Format
e-Book
Location
Online
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Clinical Reproductive Medicine and Surgery : A Practical Guide

https://libcat.nshealth.ca/en/permalink/provcat41683
Tommaso Falcone, William W. Hurd, editors. (Third edition) --Cham: Springer , 2017.
Available Online
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Location
Online
Now in a completely revised and expanded third edition, including six new chapters, this user-friendly textbook offers a succinct overview of both the medical and surgical management of reproductive disorders, as well as coverage of associated imaging modalities. Included here are updated chapters on major reproductive endocrinology and infertility issues, such as polycystic ovary syndrome (PCOS), pubertal disorders, amenorrhea, menopause, management of endometriosis and fibroids (including int…
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Other Authors
Falcone, Tommaso
Hurd, William W
Responsibility
Tommaso Falcone, William W. Hurd, editors
Edition
Third edition
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xi, 499 pages) : 118 illus., 85 illus. in color
ISBN
9783319522104
9783319522098 (print ed.)
Subjects (MeSH)
Genital Diseases, Female
Genital Diseases, Female - surgery
Reproductive Health
Abstract
Now in a completely revised and expanded third edition, including six new chapters, this user-friendly textbook offers a succinct overview of both the medical and surgical management of reproductive disorders, as well as coverage of associated imaging modalities. Included here are updated chapters on major reproductive endocrinology and infertility issues, such as polycystic ovary syndrome (PCOS), pubertal disorders, amenorrhea, menopause, management of endometriosis and fibroids (including interventional radiology), laboratory and clinical aspects of assisted reproductive technologies (ART), imaging modalities such as ultrasonography and sonohysterography, and hysteroscopic and laparoscopic techniques. New chapters include an expansion of female infertility and fertility, preimplantation diagnosis and screening, osteoporosis, and contraception and sterilization. In addition, each chapter opens with a clinical case presentation and a list of keywords relevant to the topic at hand. Residents, fellows, and new clinicians of obstetrics and gynecology interested in reproductive endocrinology and infertility will find Clinical Reproductive Medicine and Surgery: A Practical Guide a valuable and focused reference.
Contents
Hypothalamic-Pituitary-Ovarian Axis and Control of the Menstrual Cycle -- Female and Male Gametogenesis -- Normal Puberty and Pubertal Disorders -- Fertilization and Implantation -- Reproductive Imaging -- Amenorrhea -- Polycystic Ovary Syndrome -- Abnormal Uterine Bleeding -- Menopause -- Osteoporosis For The Female Patient -- Male Infertility -- Infertility -- Fertility Preservation -- Ovarian Reserve Testing -- Recurrent Early Pregnancy Loss -- Ovulation Induction -- Assisted Reproductive Technology: Clinical Aspects -- Assisted Reproductive Technology: Laboratory Aspects -- Preimplantation Genetic Diagnosis and Genetic Screening -- Hysteroscopic Management of Intrauterine Disorders: Polypectomy, Myomectomy, Endometrial Ablation, Adhesiolysis, and Removal of Uterine Septum -- Uterine Leiomyomas -- Tubal Disease and Ectopic Pregnancy -- Endometriosis -- Contraception and Sterilization -- Surgical Techniques for Management of Anomalies of the Mullerian Ducts.
Format
e-Book
Location
Online
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Diagnosis and Management of Polycystic Ovary Syndrome

https://libcat.nshealth.ca/en/permalink/provcat29176
edited by Farid, Nadir R., Evanthia Diamanti-Kandarakis. --Boston, MA: Springer-Verlag US , c2009.
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Location
Online
Available Online
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Author
Farid, Nadir R
Other Authors
Diamanti-Kandarakis, Evanthia
Responsibility
edited by Farid, Nadir R., Evanthia Diamanti-Kandarakis
Place of Publication
Boston, MA
Publisher
Springer-Verlag US
Date of Publication
c2009
ISBN
9780387097183
Subjects (MeSH)
Polycystic Ovary Syndrome - diagnosis
Polycystic Ovary Syndrome - therapy
Subjects (LCSH)
Gynecology
Format
e-Book
Location
Online
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Diet, Nutrition, and Fetal Programming

https://libcat.nshealth.ca/en/permalink/provcat41848
Rajkumar Rajendram, Victor R. Preedy, Vinood B. Patel, editors. --Cham: Humana Press , 2017.
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Location
Online
This volume offers the most comprehensive coverage on fetal programming. Chapters are written by authors of international and national standing, leaders in the field and trendsetters. The clinical relevance of the current research is emphasized in each chapter, which also contains key points, key words, and concise summaries for ease of learning. Fetal programming affects conditions in the immediate postnatal period, as well as in later life and adulthood. These conditions include cardiovascula…
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Other Authors
Rajendram, Rajkumar
Preedy, Victor R.
Patel, Vinood B.
Responsibility
Rajkumar Rajendram, Victor R. Preedy, Vinood B. Patel, editors
Place of Publication
Cham
Publisher
Humana Press
Date of Publication
2017
Physical Description
1 online resource (xxxix, 621 pages) : 154 illus., 111 illus. in color
Series
Nutrition and Health
Series Title
Nutrition and health (Totowa, N.J.)
ISBN
9783319602899
9783319602875 (print ed.)
Subjects (MeSH)
Fetal Development - physiology
Fetal Nutrition Disorders
Maternal-Fetal Exchange
Maternal Nutritional Physiological Phenomena
Abstract
This volume offers the most comprehensive coverage on fetal programming. Chapters are written by authors of international and national standing, leaders in the field and trendsetters. The clinical relevance of the current research is emphasized in each chapter, which also contains key points, key words, and concise summaries for ease of learning. Fetal programming affects conditions in the immediate postnatal period, as well as in later life and adulthood. These conditions include cardiovascular disease, frank hypertension, stroke, dyslipidemia, coagulopathy, increased insulin resistance-metabolic syndrome, type-2 diabetes, leukemia, testicular cancer, prostate cancer, breast cancer, polycystic ovary syndrome, precocious puberty, impaired immune function, renal disease, lung disease, and osteoporosis. Neuropathologies, behavioral and mental deficiencies, schizophrenia, and depression have also been reported in adults who were exposed to nutritional inadequacies in utero. Diet, Nutrition and Fetal Programming provides an overview on the effects of fetal programming on disease, and comprehensive looks at maternal nutrition factors and fetal programming effects on brain and behavior, and physiology and disease. It also provides an in depth look at specific nutrient restrictions and supplements on physiology and disease, the effects of maternal disease on fetal programming, mechanisms of programming, and a special section on the international aspects and policies on fetal programming.
Contents
Part I. Maternal Diet, Health and the Fetus: General Considerations -- Prenatal Maternal Stress in the Context: Maternal Stress Physiology, Immunology, Neuroendocrinology, Nutrition and Infant Development -- The Effects of Parental Diet on Fetal Programming of Stress-Related Brain Regions and Behaviors: Implications for Development of Neuropsychiatric Disorders -- Maternal Nutrition and Cognition -- Maternal Characteristics predisposing to Fetal Growth Restriction -- Maternal Insulin Sensitivity and Fetal Brain Activity -- Part II. Maternal Undernutrition and Protein Restriction: Effects on Fetus -- Dietary Restriction and the Endocrine Profiles in Offspring and Adults -- Maternal Undernutrition and Visceral Adiposity -- Maternal Undernutrition and Long-term Effects on Hepatic Function -- Maternal Protein Restriction and its Effects on Heart -- Effects of Maternal Protein Restriction on Nephrogenesis and Adult and Aging Kidney -- Maternal Protein Restriction and Effects on Behavior and Memory in Offspring -- Part III. Effects of Obesity, High Fat Diet and Junk Food on Fetal Outcomes -- Trends in Obesity and Implications for the Fetus -- Maternal Obesity and Implications for Fetal Programming -- Ethnicity, Obesity, and Pregnancy Outcomes on Fetal Programming -- Obesogenic Programming of Foetal Hepatic Metabolism by MircoRNAs -- Impacts of Maternal High Fat Diet on Stree-related Behavior and the Endocrine Response to Stress in Offspring -- Materna; Junk Food Diets: The Effects on Offspring Fat Mass and Food Preferences -- Part IV. Specific Dietary Components -- Maternal Fish Intake During Pregnancy and Effects on the Offspring -- Maternal Fish Oil Intake and Insulin Resistance in the Offspring -- Maternal n-3 Fatty Acids and Blood Pressure in Children -- Maternal Folate, Methyl Donors, One Carbon Metabolism, Vitamin B12 and Choline in Fetal Programming -- Maternal Taurine Supplementation Prevents Misprogramming -- Fetal Programming: Maternal Diets, Tryptophan and Postnatal Development -- Intrauterine Programming and Effects of Caffeine -- Part V. International Aspects and Policies -- Famines, Pregnancy and Effect on the Adults -- Maternal Malnutrition, Fetal Programming, Outcomes and Strategies in India -- Maternal Nutritional Factors Dictating Birth Weights: African Perspectives -- Maternal Nutrition in Ireland: Issues of Public Concern -- Maternal Malnutrition, Fetal Programming, Outcomes, and Implications of Environmental Factors in Japan -- Part VI. Effects of Fetal Programming in Childhood and Adulthood -- Growth Criteria and Predictors of Fetal Programming -- Effects of Fetal Programming on Metabolic Syndrome -- Fetal Programming of Food Preferences and Feeding Behavior -- Effects of Fetal Programming on Osteoporosis -- Childhood Sleep after Fetal Growth Restriction -- Part VII. Mechanisms of Programming -- Biomarkers of Abnormal Birth Weight in Pregnancy -- Mechanisms of Programming: Pancreatic Islets and Fetal Programming -- Pancratic GABA and Serotonin Actions in the Pancreas and Fetal Programming of Metabolism -- Maternal Malnutrition, Glucocorticoids and Fetal Programming: A Role for Placental 11ø-hydroxysteroid dehydrogenase Type 2 -- High-fat Diet and Fetal Programming: Use of p66Shc Knockouts and Implications for Human Kind -- Fetal Programming of Telomere Biology: Role of Maternal Nutrition, Obstetric Risk Factors and Suboptimal Birth Outcomes. Part VIII. Resources -- Current Research and Recommended Resources on Fetal Nutrition.
Format
e-Book
Location
Online
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Difficult cases in endourology

https://libcat.nshealth.ca/en/permalink/provcat32467
Ahmed M. Al-Kandari, Mahesh Desai, Ahmed A. Shokeir ... [et al.], editors. --London: Springer , c2013.
Available Online
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Location
Online
Endourology is an evolving subspecialty in Urology, and technological advances are ever-growing in this area. As a result, new problems arise in the workplace, that many urologists are unfamiliar with or unsure of how to resolve. It is therefore important that practising urologists have access to literature that can overcome these problems with both information and advice that is clear, concise and easy to reference. Difficult Cases in Endourology serves as an on demand reference for consultat…
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Other Authors
Al-Kandari, Ahmed M
Responsibility
Ahmed M. Al-Kandari, Mahesh Desai, Ahmed A. Shokeir ... [et al.], editors
Place of Publication
London
Publisher
Springer
Date of Publication
c2013
Physical Description
1 online resource (xvi, 346 p. : 179 ill., 100 ill. in color)
ISBN
9781848820838
Subjects (MeSH)
Endoscopy - methods
Intraoperative Complications - prevention & control
Urologic Diseases - complications
Urologic Surgical Procedures - methods
Subjects (LCSH)
Surgery
Urology
Abstract
Endourology is an evolving subspecialty in Urology, and technological advances are ever-growing in this area. As a result, new problems arise in the workplace, that many urologists are unfamiliar with or unsure of how to resolve. It is therefore important that practising urologists have access to literature that can overcome these problems with both information and advice that is clear, concise and easy to reference. Difficult Cases in Endourology serves as an on demand reference for consultation when faced with complex scenarios in the field of Endourology. Its comprehensive and accessible format make it a valuable resource for urologists at all levels, including residents, fellows and general practicing urologists.
Contents
Introduction -- Anesthetic Considerations During Endourologic Surgery -- Difficulties in Instrumentation of Endourologic Procedures -- Percutaneous Management of Calyceal Diverticula: An American Experience -- Managing Bleeding During Percutaneous Renal Surgery -- Septic Complications During Percutaneous Nephrolitholotomy (PCNL) -- Visceral Complications of Percutaneous Nephrolithotomy (PCNL) -- Percutaneous Nephrolithotomy (PCNL) for Staghorn Calculi--The Rigid Approach: Overcoming the Difficulties -- Flexible Renal Nephroscopy: Overcoming the Difficulties -- Chinese Minimally Invasive Percutaneous Nephrolithotomy (MPCNL): Overcoming the Difficulties -- Percutaneous Renal Surgery for Renal Pelvic Tumors: Overcoming the Difficulties -- Percutaneous Nephrolithotomy (PCNL) in the Treatment of Stones within Horseshoe Kidneys and in Patients with Autosomal Dominant Polycystic Kidney Disease -- Drainage Systems After Percutanous Renal Procedures -- Retrograde Nephrostomy Access: Overcoming the Difficulties -- Percutaneous Nephrolithotomy (PCNL)--The Supine Approach: Overcoming the Difficulties -- Percutaneous Nephrolithotomy (PCNL) in Obese Patients: Overcoming the Difficulties -- Percutanous Nephrolithotomy (PCNL) for Caliceal Diverticulum: An Egyptian Experience -- Endourological Management of Urological Complications Following Renal Transplantation -- Difficult Situations in Percutaneous Nephrolithotomy (PCNL) for Solitary Kidney and Renal Failure -- Percutaneous Nephrolithotomy (PCNL) and Other Simultaneous Procedures -- Adult Endopyelotomy: Overcoming the Difficulties -- Ureteroscopy for Upper Ureteral Stones: Overcoming the Difficulties of the Rigid Approach -- Uretheroscopy for Upper Ureteric and Renal Stones: Overcoming Difficulties with the Flexible Approach -- Ureteroscopy for Ureteral Strictures -- Ureteroscopic Management of Ureteral and Renal Pelvic Tumors: Overcoming the Difficulties -- Endourologic Management of Non-Malignant Bilharzial Urinary Complications -- Ureteroscopy During Pregnancy -- Pediatricá Percutaneous Nephrolithotomy (PCNL): Overcoming the Difficulties -- Pediatric Ureteroscopy: Overcoming the Difficulties -- Difficulties with Ureteral Stents -- Overcoming the Cost Difficulties in Endourology -- Difficulties in Endourologic Training -- Avoiding and Overcoming Medico-Legal Difficulties in Endourology.
Format
e-Book
Location
Online
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Endocrine Conditions in Pediatrics : A Practical Guide

https://libcat.nshealth.ca/en/permalink/provcat46360
Takara Stanley, Madhusmita Misra, editors. --Cham: Springer , c2021.
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NEW Springer 2021
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Online
This book is aimed at primary care providers who care for the pediatric age group (general pediatrician, the PCP working with pediatric patients, and family medicine providers) with the goal of covering the endocrine differential diagnosis of common signs and symptoms of possible endocrine disease as well as appropriate initial laboratory evaluation and interpretation. While multiple pediatric endocrine textbooks exist, most of them are heavy in coverage of physiology and rare diseases, with le…
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Other Authors
Stanley, Takara
Misra, Madhusmita
Responsibility
Takara Stanley, Madhusmita Misra, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2021
Physical Description
1 online resource (xvi, 381 p.) : 46 illus., 18 illus. in color
ISBN
9783030522155
9783030522148 (Print ed.)
9783030522162 (Print ed.)
Subjects (MeSH)
Child
Endocrine System Diseases
Specialty
Endocrinology
Pediatrics
Abstract
This book is aimed at primary care providers who care for the pediatric age group (general pediatrician, the PCP working with pediatric patients, and family medicine providers) with the goal of covering the endocrine differential diagnosis of common signs and symptoms of possible endocrine disease as well as appropriate initial laboratory evaluation and interpretation. While multiple pediatric endocrine textbooks exist, most of them are heavy in coverage of physiology and rare diseases, with less discussion of practical steps in evaluation and diagnosis. This book distinguishes itself through a very practical approach. The first section is organized by presenting signs and symptoms, the second section is organized by laboratory interpretation, and the third section provides summaries of common pediatric endocrine disorders. Chapters are concise, providing critical clinical information including clinical pearls, common diagnoses and important points in patient counseling. Written by experts in the field, Endocrine Conditions in Pediatrics is a valuable resource that provides general pediatricians and other primary care providers with all of the information they need to provide superb patient care before transferring to a pediatric endocrinologist when necessary.
Contents
Part I. Common Presenting Signs and Symptoms that May Reflect Endocrine Disease -- 1. Decreased Growth Velocity and/or Short Stature -- 2. Increased Growth Velocity and/or Tall Stature -- 3. Skeletal Disease -- 4. Multiple Fractures -- 5. Hypocalcemia -- 6. Hypercalcemia -- 7. Hypophosphatemia -- 8. Hypoglycemia -- 9. Hyperglycemia -- 10. Early Signs of Pubertal Development -- 11. Delayed or Stalled Pubertal Development -- 12. Atypical/Ambiguous/Non-binary Genitalia -- 13. Common Breast Complaints [Gynecomastia, Breast asymmetry, Galactorrhea] -- 14. Acne, Hirsutism, and Other Signs of Increased Androgens -- 15. Irregular Menses -- 16. Hypertension -- 17. Initial Evaluation of Polydipsia and Polyuria -- 18. Acanthosis Nigricans -- 19. Weight Gain and/or Obesity -- 20. Weight loss -- 21. Fatigue or Weakness -- 22. Dizziness or “Spells”: An Endocrine Approach -- 23. Excessive Sweating and Heat Intolerance -- Paer II. Interpretation of Endocrine Laboratory Values and Imaging -- 24. Growth Factors -- 25. Thyroid Studies -- 26. Calcium, phosphate, vitamin D, parathyroid hormone, and alkaline phosphatase -- 27. Gonadotropins, gonadal steroids, SHBG, and related labs -- 28. Sodium, Osmolality, and Antidiuretic Hormone -- 29. Adrenal Steroids, Adrenocorticotropic Hormone, and Plasma Renin Activity -- 30. Labs Related to Glucose Metabolism and Diabetes -- 31. Laboratory Evaluation of Hypoglycemia -- 32. Lipid Profiles -- 33. Prolactin -- 34. Catecholamines and Catecholamine Metabolites -- 35. Clinical Genetic Testing Options -- 36. Bone Age -- 37. Pituitary MRI -- 38. Thyroid Imaging -- 39. Bone Densitometry in Children: What Clinicians Need to Know -- Part III. Common Endocrine Conditions: Overview and Initial Management -- 40. Short Stature -- 41. Hypothyroidism -- 42. Overview and Initial Management: Hyperthyroidism -- 43. Precocious Puberty -- 44. Delayed Puberty -- 45. Polycystic Ovarian Syndrome -- 46. Disorders of Sex Development -- 47. Turner Syndrome -- 48. Klinefelter Syndrome -- 49. Adrenal Insufficiency -- 50. Overview and Initial Management of Cushing Syndrome -- 51. Persistent or Recurrent Hypoglycemia in Infants and Todlers -- 52. Type 1 Diabetes Mellitus -- 53. Overview and Initial Management of Type 2 Diabetes in Youth -- 54. Vitamin D Deficiency -- 55. Central Diabetes Insipidus (Etiology, Epidemiology and Management) -- 56.Pituitary or Suprasellar Tumors -- 57. Dyslipidemia in the Pediatric Population -- 58. Overview and Management of Childhood Obesity -- 59. Transgender Care.
Access
NEW Springer 2021
Format
e-Book
Publication Type
Handbook
Location
Online
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Ethnic Differences in Fertility and Assisted Reproduction

https://libcat.nshealth.ca/en/permalink/provcat40752
Fady I. Sharara, editor. --New York, NY: Springer , c2013.
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Over the past 10 years, studies have shown that the rates of fertility vary in different ethnic groups. Ethnic differences also play a significant role in the outcome of--and access to--assisted reproductive technology. In the United States, minority groups--African Americans, Hispanics (mainly Mexicans and Central Americans), East Asians (Chinese, Japanese, Koreans, Filipinos) and South Asians (Indians, Pakistanis, and Bengalis)--have significantly lower chances of live births compared to Cauc…
Available Online
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Other Authors
Sharara, Fady I
Responsibility
Fady I. Sharara, editor
Place of Publication
New York, NY
Publisher
Springer
Date of Publication
c2013
Physical Description
1 online resource (xiv, 255 p.)
ISBN
9781461475484
9781461475477 (print ed.)
Subjects (MeSH)
Cross-Cultural Comparison
Fertility
Health Status Disparities
Reproductive Health
Reproductive Techniques, Assisted
Abstract
Over the past 10 years, studies have shown that the rates of fertility vary in different ethnic groups. Ethnic differences also play a significant role in the outcome of--and access to--assisted reproductive technology. In the United States, minority groups--African Americans, Hispanics (mainly Mexicans and Central Americans), East Asians (Chinese, Japanese, Koreans, Filipinos) and South Asians (Indians, Pakistanis, and Bengalis)--have significantly lower chances of live births compared to Caucasian women. Birth outcome data collected by the Society for Assisted Reproductive Technology shows a worsening trend in conception rates between the years 1999-2000 and 2004-2006, raising more concern that the disparity in fertility rates between minority groups and white women is widening over time. Ethnic Differences in Fertility and Assisted Reproduction serves to answer the questions that arise when managing infertility in a multi-ethnic population. An expert assembly of key leaders in the field of Reproductive Medicine imparts insight and clinical experience in order to identify and analyze the possible causes of racial disparities in fertility outcome. Some of the reviewed causes include higher Body Mass Index (BMI), tubal diseases, metabolic syndrome, and fibroids in African Americans; tubal disease and higher early pregnancy loss in Hispanics; higher incidence of diminished ovarian reserve and lower BMI in East Asians; and higher incidence of polycystic ovarian disease (PCOS) in South Asians. A thoughtful combination of evidence-based medicine and advanced treatment options, this book is sure to distinguish itself as the definitive reference on ethnic differences in assisted reproduction.
Contents
Introduction: the scope of the topic -- Racial and ethnic groups of interest in fertility research -- The impact of socio-cultural and economic factors in seeking fertility services -- Fertility differences among ethnic groups -- Disparities between Black and White women in Assisted Reproductve Technology (ART) -- Assisted reproductive outcomes in Hispanics -- Reproductive and ART outcomes in East Asian women -- Differences in fertility and assisted reproduction in South Asian women -- Ethnicity and IVF -- Ethnic disparity in oocyte donation outcome -- Frozen embryo transfer (FET) outcomes among racial and ethnic groups -- Understanding racial disparity in adverse pregnancy outcome -- Racial diversity and uterine leiomyoma -- The effect of obesity on fertility and ART success among ethnic groups -- Polycystic ovary syndrome (PCOS) across racial and ethnic groups -- Ethnicity and ovarian response: the role of FSH receptor genotype -- Ethnic differences in fertility and assisted reproduction: ethnic disparity in stem cell availability and research -- How can we bridge the gap? Role of insurance mandate -- Editorial: Towards a better understanding of racial disparities in utilization and outcomes of IVF treatment in the United States.
Format
e-Book
Location
Online
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Female Reproductive Dysfunction

https://libcat.nshealth.ca/en/permalink/provcat45018
edited by Felice Petraglia, Bart CJM Fauser. --Cham: Springer , 2020.
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Online
Written by leading international specialists, this book provides a comprehensive, state-of-the-art overview of endocrine-based female reproductive disorders. Particularly focusing on the Hypothalamus – Pituitary – Ovary (HPO) axis as the main driver of reproduction in women, it discusses amenorrhea; chronic anovulation and polycystic ovary syndrome as the most common dysfunctions of the HPO axis; endocrine diseases as possible impacts on the HPO axis; uterine disorders related to estrogen/proge…
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Other Authors
Petraglia, Felice
Fauser, Bart CJM
Responsibility
edited by Felice Petraglia, Bart CJM Fauser
Place of Publication
Cham
Publisher
Springer
Date of Publication
2020
Physical Description
1 online resource (x, 400 p.)
Series Title
Endocrinology
Springer reference
ISBN
9783030035945
ISSN
2510-1927
Subjects (MeSH)
Endocrine System Diseases
Infertility, Female - etiology
Reproductive Health
Women's Health
Specialty
Gynecology
Reproductive Medicine
Notes
"Living reference work."
Abstract
Written by leading international specialists, this book provides a comprehensive, state-of-the-art overview of endocrine-based female reproductive disorders. Particularly focusing on the Hypothalamus – Pituitary – Ovary (HPO) axis as the main driver of reproduction in women, it discusses amenorrhea; chronic anovulation and polycystic ovary syndrome as the most common dysfunctions of the HPO axis; endocrine diseases as possible impacts on the HPO axis; uterine disorders related to estrogen/progesterone; and the impact of endometriosis and uterine fibroids on reproduction. It also addresses infertility and menopause as hormone-related disorders in women and endocrine changes during pregnancy and lactation. The book is intended as a major reference for endocrinologists, gynecologists, and obstetricians, as well as basic and clinical scientists. It is published as part of the SpringerReference program, which provides access to live editions constantly updated through a dynamic peer-review publishing process.
Contents
Abnormal Uterine Bleeding -- Assisted Reproductive Technologies -- Climacteric Syndrome -- Diagnostic Protocols for Infertility -- Endocrinology of Maternal-Placental Axis -- Endometriosis -- Hormonal Contraception -- Hormonal Treatments in the Infertile Women -- Hormone Replacement Therapy (HRT) -- Hormones and Sex Behavior -- Hormones, Breast Disorders, and Lactation -- Infertility -- Long-Term Consequences of Menopause -- Menopause and Bone Metabolism -- Menstrual Disorders Related to Endocrine Diseases -- Premature Ovarian Insufficiency -- The Hypothalamus-Pituitary-Ovary Axis -- The Menstrual Cycle and Related Disorders -- The Menstrual Disorders Related to Systemic Diseases -- The Polycystic Ovary Syndrome (PCOS) -- The “Great Obstetrical Syndromes” -- Uterine Fibroids and Adenomyosis.
Format
e-Book
Location
Online
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Fertility Preservation and Restoration for Patients with Complex Medical Conditions

https://libcat.nshealth.ca/en/permalink/provcat41687
Allison L. Goetsch, Dana Kimelman, Teresa K. Woodruff. --Cham: Springer , 2017.
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Location
Online
This unique book is a comprehensive guide for healthcare providers who treat patients with complex medical conditions but lack the resources to address fertility and sexuality concerns and help patients navigate their fertility decision-making process. It presents up-to-date information concerning fertility preservation and restoration for patients with hereditary cancer syndromes, disorders of sex development, hematologic diseases, genetic disorders of gonadal dysfunction, immunologic diseases…
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Author
Goetsch, Allison L
Other Authors
Kimelman, Dana
Woodruff, Teresa K
Responsibility
Allison L. Goetsch, Dana Kimelman, Teresa K. Woodruff
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xvii, 342 pages) : 2 illus. in color
ISBN
9783319523163
9783319523156 (print ed.)
Subjects (MeSH)
Fertility Preservation - methods
Fertility - physiology
Infertility - etiology
Infertility - therapy
Abstract
This unique book is a comprehensive guide for healthcare providers who treat patients with complex medical conditions but lack the resources to address fertility and sexuality concerns and help patients navigate their fertility decision-making process. It presents up-to-date information concerning fertility preservation and restoration for patients with hereditary cancer syndromes, disorders of sex development, hematologic diseases, genetic disorders of gonadal dysfunction, immunologic diseases, gynecologic diseases, endocrine disorders, and autoimmune and inflammatory diseases. Utilizing a practical, user-friendly format, each chapter discusses the epidemiology, classification, risk factors and/or clinical manifestations, and diagnosis and treatment modalities specific to each condition, as well as the effect of it or its treatment on fertility and unique options that may exist. Complex medical conditions are inherently difficult to manage, and reproductive interventions are often not part of the conversation. As such, Fertility Preservation and Restoration for Patients with Complex Medical Conditions will be an excellent resource for primary care physicians, obstetrician/gynecologists, endocrinologists, oncologists, and other health professionals working with patients with fertility concerns.
Contents
Options for Preserving Fertility -- Hereditary Gynecologic Cancer Predisposition Syndromes -- Disorders of the Sex Chromosomes and Sexual Development -- Malignant Hematologic Diseases -- Nonmalignant Hematologic Diseases -- Genetic Disorders Associated with Gonadal Dysfunction -- Inborn Errors of Metabolism -- Autoimmune Diseases: Rheumatic Diseases -- Autoimmune Diseases: Myasthenia Gravis and Multiple Sclerosis -- Chronic Kidney Disease -- Premature Ovarian Insufficiency -- Endometriosis -- Uterine Fibroids -- Polycystic Ovary Syndrome -- Digestive Autoimmune Diseases: Inflammatory Bowel Disease -- Breast Cancer -- Ovarian Cancer -- Endometrial Cancer -- Cervical Cancer.
Format
e-Book
Location
Online
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