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Cataract surgery

https://libcat.nshealth.ca/en/permalink/provcat32011
editor, Roger F. Steinert ; associate editors, David F. Chang ... [et al.]. (3rd ed.) --[Philadelphia]: Saunders , c2010.
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Other Authors
Steinert, Roger F
Responsibility
editor, Roger F. Steinert ; associate editors, David F. Chang ... [et al.]
Edition
3rd ed.
Place of Publication
[Philadelphia]
Publisher
Saunders
Date of Publication
c2010
Physical Description
1 online resource (xiii, 711 p.)
ISBN
9781416032250
Subjects (MeSH)
Cataract - complications
Cataract Extraction - methods
Subjects (LCSH)
Cataract - Surgery
Cataract - Surgery - Complications
Cataract Extraction - methods
Notes
"Expert consult title"--Cover
Previous ed.: 2004
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Cataract surgery

https://libcat.nshealth.ca/en/permalink/provcat50472
Steinert, Roger. (3rd ed.) --Philadelphia, PA: Elsevier , 2010.
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Location
Online
Available Online
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Author
Steinert, Roger
Edition
3rd ed.
Place of Publication
Philadelphia, PA
Publisher
Elsevier
Date of Publication
2010
ISBN
9781416032250
Subjects (MeSH)
Cataract Extraction - methods
Notes
Access to this online resource is restricted to IWK Health Centre employees working from inside the hospital network.
Format
e-Book
Location
Online
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Cataract surgery : techniques, complications, and management

https://libcat.nshealth.ca/en/permalink/provcat22690
Steinert, Roger F. (2nd ed.) --Philadelphia, PA: Saunders , 2004.
Call Number
WW 260 C357 2004
Location
Dickson Building
Call Number
WW 260 C357 2004
Author
Steinert, Roger F
Edition
2nd ed.
Place of Publication
Philadelphia, PA
Publisher
Saunders
Date of Publication
2004
Physical Description
639 p.
ISBN
0721690572
Subjects (MeSH)
Cataract Extraction
Format
Book
Location
Dickson Building
Loan Period
3 weeks
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Genetic neuromuscular disorders : a case-based approach

https://libcat.nshealth.ca/en/permalink/provcat33906
Corrado Angelini. --Cham, Switzerland: Springer , c2014.
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This book describes the genetic diagnostic entities of neuromuscular disorders. Each neuromuscular syndrome is presented clinically as a case study, accompanied by text reviewing different molecular defects, DNA research and differential diagnosis. This collection of neuromuscular disorders features the different clinical phenotypes related to each genotype and are representative of the whole spectrum of a genetic muscle disorder, helping the clinician and neuromuscular physician to make a diag…
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Author
Angelini, C.
Responsibility
Corrado Angelini
Place of Publication
Cham, Switzerland
Publisher
Springer
Date of Publication
c2014
Physical Description
1 online resource (xxi, 384 pages)
ISBN
9783319075006 (electronic bk.)
9783319074993
Subjects (MeSH)
Genetic Diseases, Inborn - Case Reports
Neuromuscular Diseases - genetics - Case Reports
Subjects (LCSH)
Neuromuscular diseases - Genetic aspects - Case studies
Neurology
Abstract
This book describes the genetic diagnostic entities of neuromuscular disorders. Each neuromuscular syndrome is presented clinically as a case study, accompanied by text reviewing different molecular defects, DNA research and differential diagnosis. This collection of neuromuscular disorders features the different clinical phenotypes related to each genotype and are representative of the whole spectrum of a genetic muscle disorder, helping the clinician and neuromuscular physician to make a diagnosis. Key points for each genetic disease are identified to suggest treatment, when available, or the main clinical exams useful in follow-up of patients. Genetic Neuromuscular Disorders: A Case-Based Approach is aimed at neuromuscular physicians and neurology residents.
Contents
Part I. Muscular Dystrophies -- Duchenne Muscular Dystrophy -- Duchenne Muscular Dystrophy Carrier -- Becker Muscular Dystrophy -- Emery-Dreifuss Muscular Dystrophy type 1 -- Emery-Dreifuss Muscular Dystrophy type 2 -- Limb Girdle Muscular Dystrophy type 1B -- Limb Girdle Muscular Dystrophy type 1C -- Limb Girdle Muscular Dystrophy type 1F -- Limb Girdle Muscular Dystrophy type 2A -- Limb Girdle Muscular Dystrophy type 2B -- Limb Girdle Muscular Dystrophy type 2C -- Limb Girdle Muscular Dystrophy type 2D -- Limb Girdle Muscular Dystrophy type 2E -- Limb Girdle Muscular Dystrophy type 2F -- Limb Girdle Muscular Dystrophy type 2I -- Limb Girdle Muscular Dystrophy type 2K -- Limb Girdle Muscular Dystrophy type 2N -- Congenital Muscular Dystrophy type 1A -- Congenital Muscular Dystrophy type 1C -- Congenital Muscular Dystrophy with rigid spine -- Congenital Muscular Dystrophy with integrin-alpha-7 deficiency -- Congenital Muscular Dystrophy, Ullrich type -- Bethlem myopathy -- Facio Scapulo Humeral Muscular Dystrophy type 1A -- Facio Scapulo Humeral Muscular Dystrophy type 2 -- Section 2: Congenital Myopathies -- Congenital Multi-Mini-Core Myopathy -- Congenital Central-Core Myopathy with Malignant Hyperthermia -- Congenital Centronuclear Myopathy type 1 -- Congenital Hyaline Body Myopathy -- Congenital Myotubular Myopathy -- Congenital Nemaline Myopathy type 2 -- Congenital Fiber Type Disproportion type 1 -- Congenital Fiber Type Disproportion -- Congenital Myofibrillar Myopathy type 1 -- Congenital Myofibrillar Myopathy type 6 -- Congenital Tubular Aggregate Myopathy -- Hereditary Inclusion Body Myopathy type 2 -- Section 3: Ion Channel Disorders -- Myotonic Dystrophy type 1, Steinert Disease -- Congenital Myotonic Dystrophy -- Myotonic Dystrophy type 2, Proximal Myotonic Myopathy -- Congenital Myotonia, Thomsen Disease -- Hyperkalemic Periodic Paralysis -- Hypokalemic Periodic Paralysis type 1 -- Slow-channel Congenital Myasthenic Syndrome -- Congenital Myasthenic Syndrome -- Brody Disease -- Section 4: Metabolic Myopathies -- Glycogenosis type 2, Pompe Disease -- Glycogenosis type 3, Cori-Forbes Disease -- Glycogenosis type 5, McArdle Disease -- Danon Disease -- Kearns-Sayre Syndrome -- Chronic Progressive External Ophthalmoplegia -- MELAS (Myopathy, Encephalopathy, Lactic Acidosis, Stroke-like) -- Leigh Syndrome due to COX Deficiency -- Mitochondrial Encephalopathy with COX Deficiency -- Coenzyme Q10 Deficiency -- Multiple Symmetrical Lipomatosis -- NARP (Neuropathy, Ataxia, Retinitis Pigmentosa) -- SANDO (Sensory Ataxic Neuropathy, Dysarthria, Ophthalmoparesis) -- Systemic Primary Carnitine Deficiency -- Neutral Lipid Storage Disease with Ichthyosis -- Neutral Lipid Storage Disease with Myopathy -- Multiple Acyl-CoA Dehydrogenase Deficiency -- Carnitine-Palmitoyl-Transferase-II Deficiency -- Niemann-Pick Disease type C1 -- Section 5: Neurogenic Disorders -- Spinal Muscular Atrophy type 1, Werdnig-Hoffmann Disease -- Spinal Muscular Atrophy type 2 -- Spinal Muscular Atrophy type 3, Kugelberg-Welander Disease -- Spinal Bulbar Muscular Atrophy, Kennedy Disease -- Charcot-Marie-Tooth Disease type 1A -- Charcot-Marie-Tooth Disease type 1B -- Charcot-Marie-Tooth Disease neuronal type -- Charcot-Marie-Tooth Disease type 4A -- Charcot-Marie-Tooth Disease with pyramidal features -- Charcot-Marie-Tooth Disease type X1 -- Distal Spinal Muscular Atrophy -- Hereditary Neuropathy with Pressure Palsies -- Friedreich Ataxia -- Spastic Ataxia, Charlevoix-Saguenay type -- Ataxia-Telangiectasia, Louis-Bar Syndrome -- Spastic Paraparesis type 4 -- Spastic Paraparesis type 7 -- Optic Atrophy Plus Syndrome -- Amyotrophic Lateral Sclerosis type 1 -- Amyotrophic Lateral Sclerosis.
Format
e-Book
Location
Online
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Ocular disease : mechanisms and management

https://libcat.nshealth.ca/en/permalink/provcat31547
[edited by] Leonard A. Levin, Daniel M. Albert. --[Philadelphia]: Saunders/Elsevier , 2010.
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Ocular Disease-a newly introduced companion volume to the classic Adlers Physiology of the Eye-correlates basic science and clinical management to describe the how and why of eye disease processes and the related best management protocols. Editors Leonard A. Levin and Daniel M. Albert-two of the world's leading ophthalmic clinician-scientists-have recruited as contributors the most expert and experienced authorities available in each of the major areas of ophthalmic disease specific to ophthalm…
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Other Authors
Levin, Leonard A
Albert, Daniel M
Responsibility
[edited by] Leonard A. Levin, Daniel M. Albert
Place of Publication
[Philadelphia]
Publisher
Saunders/Elsevier
Date of Publication
2010
Physical Description
1 online resource (xv, 687 p.)
ISBN
9780702029837
Subjects (MeSH)
Eye Diseases
Eye - physiopathology
Subjects (LCSH)
Ophthalmology
Eye - Diseases
Eye - Diseases - Treatment
Eye Diseases
Eye - physiopathology
Ophtalmologie
Œil - Maladies
Œil - Maladies - Traitement
Notes
"Expert consult"--Cover
Abstract
Ocular Disease-a newly introduced companion volume to the classic Adlers Physiology of the Eye-correlates basic science and clinical management to describe the how and why of eye disease processes and the related best management protocols. Editors Leonard A. Levin and Daniel M. Albert-two of the world's leading ophthalmic clinician-scientists-have recruited as contributors the most expert and experienced authorities available in each of the major areas of ophthalmic disease specific to ophthalmology: retina, cornea, cataract, glaucoma, uveitis, and more. The concise chapter structure features liberal use of color-with 330 full-color line artworks, call-out boxes, summaries, and schematics for easy navigation and understanding. In print and online at expertconsult.com, this comprehensive resource provides you with a better and more practical understanding of the science behind eye disease and its relation to treatment. Includes access to the fully searchable text online at expertconsult.com, along with images and references. Covers all areas of disease in ophthalmology including retina, cornea, cataract, glaucoma, and uveitis for the comprehensive information you need for managing clinical cases. Presents a unique and pragmatic blend of necessary basic science and clinical application to serve as a clinical guide to understanding the cause and rational management of ocular disease
Contents
Loss of corneal transparency / Russell L McCally -- Abnormalities of corneal wound healing / Audrey M Bernstein -- Wound healing after laser in situ keratomileusis and photorefractive keratectomy / Fabricio Witzel de Medeiros and Steven E Wilson -- Genetics and mechanisms of hereditary corneal dystrophies / John D Gottsch -- Fuchs' endothelial corneal dystrophy / Vinay Gutti, David S Bardenstein, Sudha Iyengar, and Jonathan H Lass -- Keratoconus / M Cristina Kenney and Ronald N Gaster -- Infectious keratitis / Michael S Gilmore, Susan R Heimer, and Ai Yamada -- Corneal graft rejection / Daniel R Saban, Mohammad H Dastjerdi, and Reza Dana -- Corneal edema / Daniel G Dawson and Henry F Edelhauser -- Corneal angiogenesis and lymphangiogenesis / Chih-Wei Wu, David Ellenberg, and Jin-Hong Chang -- Ocular surface restoration / Julie T Daniels, Genevieve A Secker, and Alex J Shortt -- Herpetic keratitis / Pranita P Sarangi and Barry T Rouse -- Ocular allergy / Neal P Barney, Ellen B Cook, James L Stahl, and Frank M Graziano -- The lacrimal gland and dry-eye disease / Darlene A Dartt -- Immune mechanisms of dry-eye disease / Austin K Mircheff and Joel E Schechter -- Disruption of tear film and blink dynamics / Jianhua Wang and Anuj Chauhan -- Abnormalities of eyelid and tear film lipid / Gary N Foulks and Douglas Borchman -- Dry eye: abnormalities of tear film mucins / Ann-Christin Albertsmeyer and Ilene K Gipson -- Steroid-induced glaucoma / Abbot F Clark, Xinyu Zhang, and Thomas Yorio -- Biomechanical changes of the optic disc / Ian A Sigal, Michael D Roberts, Michael JA Girard, Claude F Burgoyne, and J Crawford Downs -- Pigmentary dispersion syndrome and glaucoma / Michael G Anderson -- Abnormal trabecular meshwork outflow / Paul A Knepper and Beatrice YJT Yue -- Pressure-induced optic nerve damage / James C Tsai -- Exfoliation (pseudoexfoliation) syndrome / Robert Ritch and Ursula Schultzer-Schrehardt -- Angle closure glaucoma / Shamira Perera, Nishani Amerasinghe, and Tin Aung -- Central nervous system changes in glaucoma / Yeni N Yücel and Neeru Gupta -- Retinal ganglion cell death in glaucoma / Heather R Pelzel and Robert W Nickells -- Wound-healing responses to glaucoma surgery / Stelios Georgoulas, Annegret Dahlmann-Noor, Stephen Brocchini, and Peng Tee Khaw -- Blood flowchanges in glaucoma / Leopold Schmetterer and Mark Lesk -- Biochemical mechanisms of age-related cataract / David C Beebe, Ying-Bo Shui, and Nancy M Holekamp -- Posterior capsule opacification / Judith West-Mays and Heather Sheardown -- Diabetes-associated cataracts / Peter F Kador -- Steroid-induced cataract / Abbas Samadi -- Presbyopia / Jane F Koretz -- Restoration of accommodation / Stephen D McLeod and Michelle Trager Cabrera -- Intraoperative floppy iris syndrome / Amy Lin and Roger F Steinert -- Optic neuritis / John R Guy and Xiaoping Qi -- Abnormal ocular motor control / James A Sharpe and Arun Sundaram -- Idiopathic intracranial hypertension (idiopathic pseudotumor cerebri) / Deborah M Grzybowski and Martin Lubow -- Giant cell arteritis / Lynn K Gordon -- Ischemic optic neuropathy / Helen Danesh-Meyer -- Optic nerve axonal injury / Daniela Toffoli and Leonard A Levin -- Leber's hereditary optic neuropathy / Alfredo Sadun and Alice Kim -- Optic atrophy / Nathan T Tagg and Randy H Kardon -- Nystagmus / Frank Proudlock and Irene Gottlob -- Toxic optic nerve neuropathies / FT "Fritz" Fraunfelder and FW "Rick" Fraunfelder -- Uveal melanoma / Zelia MS Correa and J William Harbour -- Genetics of hereditary retinoblastoma / Alejandra G de Alba Campomanes and Joan M O'Brien -- Molecular basis of low-penetrance retinoblastoma / Katie Matatall and J William Harbour -- Vasculogenic mimicry / Robert Folberg and Andrew J Maniotis -- Treatment of choroidal melanoma / Aimee V Chappelow and Andrew P Schachat -- Sebaceous cell carcinoma / Alon Kahana, Jonathan T Pribila, Christine C Nelson, and Victor M Elner -- Neurofibromatosis / Robert Listernick and David H Gutmann -- Phthisis bulbi / Ingo Schmack, Hans E Volcker, and Hans E Grossniklaus -- Myopia / Terri L Young -- Pathogenesis of Graves' ophthalmopathy / A Reagan Schiefer and Rebecca S Bahn -- Duane syndrome / Joseph L Demer -- Amblyopia / Robert F Hess and Nigel Daw -- Strabismus / Christopher S von Bartheld, Scott A Croes, and L Alan Johnson -- Albinism / Gerald F Cox and Anne B Fulton -- Aniridia / Elias I Traboulsi -- Color vision defects / Maureen Neitz and Jay Neitz -- Acute retinal vascular occlusive disorders / Sohan Singh Hayreh -- Retinal photic injury: laboratory and clinical findings / Daniel Organisciak and Marco Zarbin -- Vascular damage in diabetic retinopathy / Timothy S Kern and Suber Huang -- Neovascularization in diabetic retinopathy / Corey B Westerfeld and Joan W Miller -- Diabetic macular edema / Pascale Massin, Michel Paques, and Jean-Antoine Pournaras --Dry age-related macular degeneration and age-related macular degeneration pathogenesis / Marco Zarbin and Janet S Sunness -- Neovascular age-related macular degeneration / David E Lederer, Scott W Cousins, and Karl G Csaky -- Inhibition of / Anthony P Adamis and Adrienne Berman -- Retinal detachment / Steven K Fisher and Geoffrey P Lewis -- Retinopathy of prematurity / Mary Elizabeth Hartnett and Cynthia A Toth -- Retinal energy metabolism / Robert A Linsenmeier -- Retinitis pigmentosa and related disorders / Eric A Pierce -- Visual prostheses and other assistive devices / Muhammad Ali Memon and Joseph F Rizzo III -- Paraneoplastic retinal degeneration / Grazyna Adamus -- Cellular repopulation of the retina / Budd AL Tucker, Michael J Young, and Henry J Klassen -- Proliferative vitreoretinopathy / Clyde Guidry -- Immunologic mechanisms of uveitis / Steven Yeh, Zhuqing Li, and Robert B Nussenblatt -- Herpesvirus retinitis / Sally S Atherton and Mei Zheng -- Sympathetic ophthalmia / Mirunalini Kumaradas and Narsing A Rao -- Scleritis / Srilakshmi M Sharma and James T Rosenbaum -- Infectious uveitis / Pooja Bhat, Allen Tony Jackson, and C Stephen Foster -- Ocular sarcoidosis / Russell N Van Gelder and Suzanne M Dintzis
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