topic:"Prenatal Diagnosis" found 29 records - Provincial Hospitals Library Catalogue

Atlas of Genetic Diagnosis and Counseling

https://libcat.nshealth.ca/en/permalink/provcat30009

by Harold Chen. --Totowa, NJ: Humana Press , c2006.

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Location: Online

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Author: Chen, Harold

Responsibility: by Harold Chen

Place of Publication: Totowa, NJ

Publisher: Humana Press

Date of Publication: c2006

ISBN: 9781603271615

Subjects (MeSH): Genetic counseling; Genetic Diseases, Inborn - Encyclopedias; Prenatal Diagnosis

Subjects (LCSH): Genetics; Reproductive medicine

Format: e-Book

Location: Online

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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Location: Online

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

Atlas of genetic diagnosis and counseling

https://libcat.nshealth.ca/en/permalink/provcat22395

Chen, Harold. --Totowa, NJ: Humana Press , 2006.

Call Number: QZ 17 C518a 2006

Location: Halifax Infirmary

Call Number: QZ 17 C518a 2006

Author: Chen, Harold

Place of Publication: Totowa, NJ

Publisher: Humana Press

Date of Publication: 2006

Physical Description: 1076 p.

ISBN: 1588296814

Subjects (MeSH): Prenatal Diagnosis; Genetic counseling; Genetic Diseases, Inborn - Atlases

Format: Book

Location: Halifax Infirmary

Loan Period: 3 weeks

Caffey's pediatric diagnostic imaging

https://libcat.nshealth.ca/en/permalink/provcat33013

editor, Brian D. Coley. (13th ed.) --Philadelphia, PA: Elsevier , c2019.

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Access: Registration required for PDF access.

Location: Online

For more than 70 years, Caffey’s Pediatric Diagnostic Imaging has been the comprehensive, go-to reference that radiologists have relied upon for dependable coverage of all aspects of pediatric imaging. In the 13th Edition, Dr. Brian Coley leads a team of experts to bring you up to date with today’s practice standards in radiation effects and safety, as well as in head and neck, neurologic, thoracic, cardiac, gastrointestinal, genitourinary, and musculoskeletal pediatric imaging. This two-volum…

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Other Authors: Coley, Brian D.

Responsibility: editor, Brian D. Coley

Edition: 13th ed.

Alternate Title: Pediatric diagnostic imaging; Caffey's paediatric diagnostic imaging; Paediatric diagnostic imaging

Place of Publication: Philadelphia, PA

Publisher: Elsevier

Date of Publication: c2019

Physical Description: 1 online resource (1648 p.)

ISBN: 9780323497480

Subjects (MeSH): Child; Diagnostic Imaging - methods; Fetal Diseases - diagnosis; Infant; Prenatal Diagnosis - methods

Specialty: Diagnostic Imaging; Pediatrics

Abstract: For more than 70 years, Caffey’s Pediatric Diagnostic Imaging has been the comprehensive, go-to reference that radiologists have relied upon for dependable coverage of all aspects of pediatric imaging. In the 13th Edition, Dr. Brian Coley leads a team of experts to bring you up to date with today’s practice standards in radiation effects and safety, as well as in head and neck, neurologic, thoracic, cardiac, gastrointestinal, genitourinary, and musculoskeletal pediatric imaging. This two-volume bestselling reference is a must-have resource for pediatric radiologists, general radiologists, pediatric subspecialists, pediatricians, hospitals, and more - anywhere clinicians need to ensure safe, effective, and up-to-date imaging of children.

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Format: e-Book

Location: Online

Caring for children born small for gestational age

https://libcat.nshealth.ca/en/permalink/provcat33545

editor-in-chief: Siegfried Zabransky ; contributors: Miguel Alejandre Alcázar [and others]. --London: Springer Healthcare , c2013.

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Location: Online

Care for Children Born Small for Gestational Age is a comprehensive handbook that serves to synthesize the extensive recent literature in the area to provide a practical resource aimed at a wide range of healthcare professionals, including obstetricians, midwives, neonatologists, and primary care physicians. This comprehensive handbook includes an in-depth survey of the prevention, diagnosis, treatment and long-term monitoring of children born small for gestational age, as well as related condi…

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Other Authors: Zabransky, Siegfried

Responsibility: editor-in-chief: Siegfried Zabransky ; contributors: Miguel Alejandre Alcázar [and others]

Place of Publication: London

Publisher: Springer Healthcare

Date of Publication: c2013

Physical Description: 1 online resource (xvii, 299 pages)

ISBN: 9781908517906 (electronic bk.); 9781908517852

Subjects (MeSH): Fetal Development; Fetal Growth Retardation; Infant Care; Infant, Low Birth Weight; Prenatal Diagnosis

Abstract: Care for Children Born Small for Gestational Age is a comprehensive handbook that serves to synthesize the extensive recent literature in the area to provide a practical resource aimed at a wide range of healthcare professionals, including obstetricians, midwives, neonatologists, and primary care physicians. This comprehensive handbook includes an in-depth survey of the prevention, diagnosis, treatment and long-term monitoring of children born small for gestational age, as well as related conditions such as intrauterine growth restriction, metabolic syndrome and type 2 diabetes. Additionally, the short and long-term psychiatric and social consequences of this condition are addressed.

Contents: Fetal Development -- Intrauterine aspects -- Maternal nutrition -- Prenatal care, surveillance, and risk assessment -- Birthweight percentiles: an international comparison -- Fetal growth restriction: definitions, causes, and epidemiology -- Obstetric aspects -- Placental function in intrauterine growth restriction -- Placental function: predicting impairment -- The role of genetic and epigenetics in growth restriction -- Fetal programming -- Premature infants -- Term newborns -- Endocrine regulation of fetal growth -- Growth hormone treatment -- Renal function -- Pancreatic development -- Metabolic syndrome -- Cardiovascular risks and diseases -- Ophthalmological findings and visual function disorders -- Auditory function disorders -- Neurological, neurocognitive and behavioural aspects -- Prevention and long term care -- Considerations for future research.

Format: e-Book

Location: Online

Clinical obstetrics : the fetus & mother

https://libcat.nshealth.ca/en/permalink/provcat53057

Reece, E. Albert. (3rd ed.) --Malden, MA: Blackwell Publishing , 2007.

Call Number: WQ 211 C641 2007

Location: IWK Health Sciences Library

Call Number: WQ 211 C641 2007

Author: Reece, E. Albert

Other Authors: Hobbins, John C.

Edition: 3rd ed.

Place of Publication: Malden, MA

Publisher: Blackwell Publishing

Date of Publication: 2007

Physical Description: 168 p.

ISBN: 9.78E+12

Subjects (MeSH): Fetal Diseases; Embryonic Development; Fetal Development; Maternal-Fetal Exchange; Pregnancy - physiology; Pregnancy Complications; Prenatal Diagnosis

Format: Book

Location: IWK Health Sciences Library

Copies: 1

Loan Period: 2 weeks

Creasy and Resnick's maternal-fetal medicine : principles and practice

https://libcat.nshealth.ca/en/permalink/provcat42414

editors, Robert K. Creasy ... [et al.]. (8th ed.) --Philadelphia, PA: Elsevier , c2019.

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Location: Online

Long recognized as the authoritative leader in the field, Creasy and Resnik's Maternal-Fetal Medicine, 8th Edition, continues to provide the latest evidence-based guidelines for obstetric and neonatal management, helping you minimize complications and offer patients the best possible care. Written by renowned experts in obstetrics, gynecology, and perinatology, this comprehensive resource has been thoroughly updated and reflects new information in every area, including recent tremendous advanc…

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Other Authors: Creasy, Robert K.

Responsibility: editors, Robert K. Creasy ... [et al.]

Edition: 8th ed.

Alternate Title: Maternal-fetal medicine

Place of Publication: Philadelphia, PA

Publisher: Elsevier

Date of Publication: c2019

Physical Description: 1 online resource, 1408 p.

ISBN: 9780323479103

Subjects (MeSH): Pregnancy - physiology; Prenatal Diagnosis; Pregnancy Complications; Fetal Diseases; Fetus - physiology

Specialty: Maternal Health; Perinatology

Abstract: Long recognized as the authoritative leader in the field, Creasy and Resnik's Maternal-Fetal Medicine, 8th Edition, continues to provide the latest evidence-based guidelines for obstetric and neonatal management, helping you minimize complications and offer patients the best possible care. Written by renowned experts in obstetrics, gynecology, and perinatology, this comprehensive resource has been thoroughly updated and reflects new information in every area, including recent tremendous advances in genetics, imaging, and more.

Contents: Part 1: Scientific basis of perinatal biology. Human basic genetics and patterns of inheritance -- Molecular genetic technology -- Normal early development -- Amniotic fluid dynamics -- Multiple gestation: the biology of twinning -- Physiology of parturition -- Pathogenesis of spontaneous preterm birth -- Immunology of pregnancy -- Maternal cardiovascular, respiratory, and renal adaptation to pregnancy -- Endocrinology of pregnancy -- The breast and the physiology of lactation -- Maternal nutrition -- Fetal cardiovascular physiology -- Behavioral states in the fetus: relationship to fetal health and development -- Placental respiratory gas exchange and fetal oxygenation -- Fetal lung development and surfactant -- Evidence-based practice in perinatal medicine -- Part 2: Obstetric imaging. Section I: Principles of fetal imaging. Performing and documenting the fetal anatomy ultrasound examination -- Doppler ultrasound: select fetal and maternal applications -- Clinical applications of three-dimensional sonography in obstetrics -- MRI in obstetrical imaging -- Section II: Lesions. Central nervous system imaging -- Cephalocele -- Choroid plexus cysts -- Holoprosencephaly -- Porencephalic cyst -- Ventriculomegaly: aqueductal stenosis -- Ventriculomegaly: arnold-chiari malformation -- Ventriculomegaly: borderline lateral cerebral ventriculomegaly -- Ventriculomegaly: dandy-walker malformation and variant -- Agenesis of the corpus callosum -- Arachnoid cyst -- Exencephaly and anencephaly -- Hydranencephaly -- Microcephaly -- Vein of Galen aneurysm -- Imaging of the face and neck -- Cleft lip and palate -- Cystic hygroma -- Micrognathia -- Abnormal orbits -- Goiter -- Thoracic imaging -- Congenital diaphragmatic hernia -- Cystic lung lesions, CPAM/CCAM, and sequestration -- Congenital high airway obstruction -- Pleural effusion -- Fetal cardiac malformations and arrhythmias: detection, diagnosis, management, and prognosis -- Abdominal imaging -- Abdominal ascites -- Intestinal atresias -- Gastroschisis -- Omphalocele -- Cystic abdominal lesions -- Echogenic abdominal lesions -- Limb-body stalk lesions -- Umbilical vein varix -- Esophageal atresia -- Urogenital imaging -- Skeletal imaging -- Placenta and umbilical cord imaging -- Marginal and velamentous umbilical cord insertion -- Molar gestation -- Placenta accreta-increta-percreta -- Placental echolucencies: lakes, cysts, chorangioma -- Placenta previa -- Single umbilical artery -- Amniotic fluid volume -- Circumvallate placenta -- Subchorionic hematoma -- Succenturiate placenta -- Vasa previa -- Uterus and adnexae imaging -- Adnexal mass, complex and simple -- Uterine anomalies -- Uterine myomas -- First-trimester imaging -- Fetal structural anomalies -- Nuchal translucency -- Nasal bone -- Part 3: Fetal disorders: diagnosis and therapy. Prenatal diagnosis of congenital disorders -- Teratogenesis and environmental exposure -- Assessment of fetal health -- Intrapartum fetal surveillance -- Assessment and induction of fetal pulmonary maturity -- Invasive fetal therapy -- Hemolytic disease of the fetus and newborn -- Nonimmune hydrops -- Multiple gestation: clinical characteristics and management -- Part 4: Disorders at the maternal-fetal interface. Prevention and management of preterm parturition -- Premature rupture of the membranes -- Clinical aspects of normal and abnormal labor -- Recurrent pregnancy loss -- Stillbirth -- Placenta previa, placenta accreta, abruptio placentae, and vasa previa -- Intrauterine growth restriction -- Pregnancy-related hypertension -- Part 5: Maternal complications. Patient safety in obstetrics -- Maternal mortality -- Maternal and fetal infections -- Cardiac diseases -- Coagulation disorders in pregnancy -- Thromboembolic disease in pregnancy -- Anemia and pregnancy -- Malignancy and pregnancy -- Renal disorders -- Respiratory diseases in pregnancy -- Diabetes in pregnancy -- Obesity in pregnancy -- Thyroid disease and pregnancy -- Other endocrine disorders of pregnancy -- Gastrointestinal disease in pregnancy -- Diseases of the liver, biliary system, and pancreas -- Pregnancy and rheumatic diseases -- Neurologic disorders -- Management of depression and psychoses in pregnancy and in the puerperium -- Substance abuse in pregnancy -- The skin and pregnancy -- Anesthesia considerations for complicated pregnancies -- Intensive care considerations for the critically ill parturient -- Pregnancy as a window to future health -- Part 6: The neonate. Neonatal morbidities of prenatal and perinatal origin.

Format: e-Book

Location: Online

Creasy and Resnik's maternal-fetal medicine : principles and practice

https://libcat.nshealth.ca/en/permalink/provcat32276

editors, Robert K. Creasy, Robert Resnik, Michael F. Greene, Jay D. Iams, Charles J. Lockwood, Thomas R. Moore. (Seventh edition) --[s.l.]: Saunders , 2014.

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Location: Online

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Other Authors: Creasy, Robert K; Resnik, Robert; Greene, Michael F; Iams, Jay D; Lockwood, Charles J

Responsibility: editors, Robert K. Creasy, Robert Resnik, Michael F. Greene, Jay D. Iams, Charles J. Lockwood, Thomas R. Moore

Edition: Seventh edition

Alternate Title: Creasy & Resnik's maternal-fetal medicine

Place of Publication: [s.l.]

Publisher: Saunders

Date of Publication: 2014

Physical Description: 1 online resource

ISBN: 9781455711376

Subjects (MeSH): Fetal Diseases; Fetus - physiology; Pregnancy - physiology; Pregnancy Complications; Prenatal Diagnosis

Subjects (LCSH): Pregnancy - Complications - Handbooks, manuals, etc; Fetal Diseases; Fetus - physiology; Pregnancy - physiology; Pregnancy Complications; Prenatal Diagnosis

Notes: Preceded by: Creasy & Resnik's maternal-fetal medicine : principles and practice / editors, Robert K. Creasy, Robert Resnik, Jay D. Iams ; associate editors, Charles J. Lockwood, Thomas R. Moore. 6th ed. c2009.

Access: Registration required for PDF access.

Format: e-Book

Location: Online

Creasy and Resnik's maternal-fetal medicine : principles and practice

https://libcat.nshealth.ca/en/permalink/provcat50570

Creasy, Robert. (8th ed.) --Philadelphia, PA: Elsevier , 2019.

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Location: Online

Available Online: View e-Book

Author: Creasy, Robert

Edition: 8th ed.

Place of Publication: Philadelphia, PA

Publisher: Elsevier

Date of Publication: 2019

ISBN: 9780323479103

Subjects (MeSH): Fetal Diseases; Fetus - physiology; Pregnancy - physiology; Pregnancy Complications; Prenatal Diagnosis

Notes: Access to this online resource is restricted to IWK Health Centre employees working from inside the hospital network.

Format: e-Book

Location: Online

Creasy and Resnik's maternal-fetal medicine : principles and practice

https://libcat.nshealth.ca/en/permalink/provcat53133

Creasy, Robert K. (6th ed.) --Philadelphia, PA: Saunders , 2009.

Call Number: WQ 211 M425 2009

Location: IWK Health Sciences Library

Call Number: WQ 211 M425 2009

Author: Creasy, Robert K.

Other Authors: Resnik, Robert; Iams, Jay D.

Edition: 6th ed.

Place of Publication: Philadelphia, PA

Publisher: Saunders

Date of Publication: 2009

Physical Description: 1282 p.

ISBN: 9.78E+12

Subjects (MeSH): Prenatal Diagnosis; Pregnancy Complications; Fetal Diseases; Pregnancy - physiology; Pregnancy, High-Risk

Notes: The most recent edition of this book is available online. Visit:; https://www.clinicalkey.com/#!/browse/book/3-s2.0-C20160000049

Format: Book

Location: IWK Health Sciences Library

Copies: 1

Loan Period: 2 weeks

Fetal Cardiology : A Practical Approach to Diagnosis and Management

https://libcat.nshealth.ca/en/permalink/provcat42683

John Simpson, Vita Zidere, Owen I. Miller, editors. --Cham: Springer , c2018.

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Location: Online

This practical book describes a systematic approach to the ultrasound examination of the fetal heart based on accepted screening recommendations. The written content is enhanced by images and videos of both normal and abnormal sonographic findings. Fetal Cardiology: A Practical Approach to Diagnosis and Management goes further than simply describing core screening views. It includes extended views of the fetal heart, the use of Doppler techniques and assessment of fetal cardiac function. "Varia…

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Other Authors: Simpson, John; Zidere, Vita; Miller, Owen I.

Responsibility: John Simpson, Vita Zidere, Owen I. Miller, editors

Place of Publication: Cham

Publisher: Springer

Date of Publication: c2018

Physical Description: 1 online resource (xxviii, 308 p.) : 248 illus., 186 illus. in color

ISBN: 9783319774619; 9783319774602 (print ed.); 9783319774626 (print ed.); 9783030084608 (print ed.)

Subjects (MeSH): Fetal Heart - physiopathology; Heart Diseases - diagnosis; Heart Diseases - therapy; Infant, Newborn; Prenatal Diagnosis

Specialty: Cardiology; Embryology

Abstract: This practical book describes a systematic approach to the ultrasound examination of the fetal heart based on accepted screening recommendations. The written content is enhanced by images and videos of both normal and abnormal sonographic findings. Fetal Cardiology: A Practical Approach to Diagnosis and Management goes further than simply describing core screening views. It includes extended views of the fetal heart, the use of Doppler techniques and assessment of fetal cardiac function. "Variants" which can be encountered in practice are described as well as the features of the major groups of cardiac abnormalities and fetal arrhythmias. Because the authors include experienced fetal and paediatric cardiologists, the focus is not only on diagnostic features but also the approach to postnatal care and prognosis. This content is enhanced by inclusion of chapters relating to associated fetal abnormalities, the genetics of congenital heart disease and new imaging modalities such as MRI of the fetal heart. The book equips all those using ultrasound to image the fetus with a clear concise reference to meet the challenge of new guidelines and to expand their knowledge of complementary echocardiographic techniques and management. It details why prenatal recognition of congenital heart disease is being prioritised to allow for parental choice, recognition of associated abnormalities and improvement of postnatal outcome. As such, this book will be important for all professionals, whether they be a cardiologist, fetal medicine specialist, sonographer or midwife.

Contents: 1. Organisation of Screening for Congenital Heart Disease -- 2. Screening Views of the Fetal Heart -- 3. Extended Views of the Fetal Heart -- 4. Use of Doppler Techniques in Fetal Echocardiography -- 5. Fetal Cardiac Function -- 6. First Trimester Fetal Echocardiography -- 7. Abnormalities of the Four Chamber View -- 8. Abnormalities of the Great Arteries -- 9. Aortic Arch Abnormalities -- 10. Abnormalities of the Systemic and Pulmonary Veins -- 11. Fetal Arrhythmias -- 12. Role of Fetal Cardiac Magnetic Resonance Imaging -- 13. Counselling Following a Prenatal Diagnosis of Congenital Heart Disease -- 14. Fetal Abnormalities Associated with Congenital Heart Defects -- 15. Genetics of Congenital Heart Disease -- 16. Impact of Prenatal Diagnosis of Congenital Heart Disease on Outcome -- 17. Obstetric and Fetal Medicine Management of the Fetus with Congenital Heart Disease -- 18. Post-Natal Cardiac Management of the Fetus with Congenital Heart Disease.

Format: e-Book

Location: Online

Fetal medicine : basic science and clinical practice

https://libcat.nshealth.ca/en/permalink/provcat32162

by Pranav P. Pandya, Ronald Wapner, Dick Oepkes, and Neil Sebire. (3rd ed.) --London, UK: Elsevier , c2020.

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Location: Online

Covering pertinent basic science and offering today’s most authoritative guidance on clinical management, Fetal Medicine, 3rd Edition, is a must-have resource for obstetricians and other healthcare professionals involved in care of the fetus. An international team of expert contributors delivers the knowledge and background you need to effectively diagnose and treat fetal disorders - everything from prenatal screening and diagnostic tests to common and rare prenatal conditions, early pregnancy…

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Author: Pandya, Pranav P.

Other Authors: Wapner, Ronald

Responsibility: by Pranav P. Pandya, Ronald Wapner, Dick Oepkes, and Neil Sebire

Edition: 3rd ed.

Place of Publication: London, UK

Publisher: Elsevier

Date of Publication: c2020

Physical Description: 1 online resource, 640 p.

ISBN: 9780702069567

Subjects (MeSH): Fetal Diseases - diagnosis; Fetal Diseases - therapy; Fetal monitoring; Fetus - physiology; Prenatal Diagnosis

Subjects (LCSH): Fetus - Diseases; Fetus - Physiology; Fetus - Abnormalities; Fetal monitoring; Prenatal diagnosis; Fetal Diseases - diagnosis; Fetal Diseases - therapy; Fetal Monitoring; Fetus - physiology; Prenatal Diagnosis

Specialty: Embryology; Perinatology

Abstract: Covering pertinent basic science and offering today’s most authoritative guidance on clinical management, Fetal Medicine, 3rd Edition, is a must-have resource for obstetricians and other healthcare professionals involved in care of the fetus. An international team of expert contributors delivers the knowledge and background you need to effectively diagnose and treat fetal disorders - everything from prenatal screening and diagnostic tests to common and rare prenatal conditions, early pregnancy loss, ethical issues, and much more.

Access: Registration required for PDF access.

Format: e-Book

Location: Online

Fetal medicine : basic science and clinical practice

https://libcat.nshealth.ca/en/permalink/provcat50702

Pandya, Pranav P. (3rd ed.) --Philadelphia, PA: Elsevier , 2020.

Available Online: View e-Book

Location: Online

Available Online: View e-Book

Author: Pandya, Pranav P.

Other Authors: Oepkes, Dick; Sebire, Neil J.; Wapner, Ronald J.

Edition: 3rd ed.

Place of Publication: Philadelphia, PA

Publisher: Elsevier

Date of Publication: 2020

ISBN: 9780702072871

Subjects (MeSH): Fetal Diseases - diagnosis; Fetal Diseases - therapy; Fetal monitoring; Fetus - physiology; Prenatal Diagnosis

Notes: Access to this online resource is restricted to IWK Health Centre employees working from inside the hospital network.

Format: e-Book

Location: Online

Fetal Morph Functional Diagnosis

https://libcat.nshealth.ca/en/permalink/provcat46487

Hideaki Masuzaki, editor. --Singapore: Springer , c2021.

Available Online: View e-Book

Access: NEW Springer 2021

Location: Online

This book explores the recent clinical and research findings in the field of prenatal screening and diagnosis. It presents new devices and tests such as real-time 3D ultrasound, ultrafast fetal MRI, and next-generation sequencing and discusses genetic counseling and fetal therapy. Written by pioneering scientists, the book is divided into six themed parts: ultrasound examination, genetic tests, genetic disorders, chromosomal diseases, genetic counseling, and techniques, presenting carefully pre…

Available Online: View e-Book

Other Authors: Masuzaki, Hideaki

Responsibility: Hideaki Masuzaki, editor

Place of Publication: Singapore

Publisher: Springer

Date of Publication: c2021

Physical Description: 1 online resource (ix, 354 p.) : 108 illus., 60 illus. in color

Series Title: Comprehensive gynecology and obstetrics

ISBN: 9789811581717; 9789811581700 (Print ed.); 9789811581724 (Print ed.); 9789811581731 (Print ed.)

ISSN: 2364-1932

Subjects (MeSH): Chromosome Disorders; Fetus - abnormalities; Genetic Counseling; Prenatal Diagnosis - methods

Specialty: Embryology; Reproductive Medicine

Abstract: This book explores the recent clinical and research findings in the field of prenatal screening and diagnosis. It presents new devices and tests such as real-time 3D ultrasound, ultrafast fetal MRI, and next-generation sequencing and discusses genetic counseling and fetal therapy. Written by pioneering scientists, the book is divided into six themed parts: ultrasound examination, genetic tests, genetic disorders, chromosomal diseases, genetic counseling, and techniques, presenting carefully prepared original data.This thought-provoking, instructive and informative book is intended for geneticists, obstetricians, pediatricians, genetic counselors and nurses. Although the incidence of congenital abnormalities such as structural, chromosomal and genetic disorders is very low, it is important to have accurate information on their incidence and likely outcome, and on the screening and diagnosis of congenital abnormalities during pregnancy care. This book provides valuable insights into prenatal screening, genetic counseling and fetal diagnosis.

Contents: Part I. Ultrasound Examination -- 1. Ultrasonic Screening -- 2. Abnormal Findings in Ultrasound Examination -- 3. Fetal MRI -- Part II. Genetic Tests -- 4. Prenatal Screening for Fetal Aneuploidy -- 5. Diagnostic Tests (Invasive Procedures) -- Part III. Genetic Disorders -- 6. Mendelian Disease -- 7. Neuroimaging and Genetics in Brain Maldevelopment -- 8. Muscular Dystrophy -- 9. Skeletal Dysplasia 10. Genitourinary Tract Abnormalities -- 11. Genomic Imprinting Disorders (Including Mesenchymal Placental Dysplasia) -- 12. Genetics in Multiple Gestation -- 13. Fetal Therapy -- Part IV. Chromosomal Diseases -- 14. General Remarks About Autosomal Diseases -- 15. Sex Chromosome-Linked Diseases -- Part V. Genetic Counseling -- 16. Fetal Anomaly and Genetic Counseling -- 17. Soft Marker Test (NT, Nasal Bone, Etc.) and Genetic Counseling -- 18. Noninvasive Prenatal Testing and Genetic Counseling -- 19. Trisomy and Genetic Counseling -- 20. Sex Chromosome Abnormalities and Genetic Counseling -- 21. Genetic Counseling: Chromosomal Structural Rearrangements -- 22. Gene Disorders and Genetic Counseling -- Part VI. Technical -- 23. G-Banding: Fetal Chromosome Analysis by Using Chromosome Banding Techniques -- 24. FISH -- 25. Polymerase Chain Reaction (PCR) -- 26. Microarray and Next Generation Sequencing -- 27. How to Obtain Certifications and Licenses for Prenatal Diagnosis.