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Retinal Degenerative Diseases
Title
Retinal Degenerative Diseases [electronic resource] / edited by Joe G. Hollyfield, Robert E. Anderson, Matthew M. LaVail.
ISBN
9780387324425
Edition
1st ed. 2006.
Publication
New York, NY : Springer US : Imprint: Springer, 2006.
Physical Description
1 online resource (XXII, 557 p.)
Local Notes
Access is available to the Yale community.
Access and use
Access restricted by licensing agreement.
Summary
Retinal Degenerations is the result of the International Symposium on Retinal degeneration which has become perhaps the most important research meeting in the field. THe topics in this volume explore the etiology, cellular mechanisms, epidemiology, genetics, models and potential therapeutic measures for the blinding diseases of retinitis pigmentosa and age-related macular degeneration.
Variant and related titles
Springer ENIN.
Other formats
Printed edition:
Printed edition:
Printed edition:
Format
Books / Online
Language
English
Added to Catalog
September 25, 2019
Contents
From the contents Genetic Factors Modifying Clinical Expression of Autosomal Dominant Rp
Disease-Associated Variants of The Rod-Derived Cone Viability Factor (Rdcvf) In Leber Congenital Amaurosis. Rod-Derived Cone Viability Variants in Lca
Leber Congenital Amaurosis: Survey of The Genetic Heterogeneity, Refinement of The Clinical Definition and Phenotype-Genotype Correlations as A Strategy For Molecular Diagnosis. Clinical and Molecular Survey in Lca
A First Locus For Isolated Autosomal Recessive Optic Atrophy (Roa1) Maps To Chromosome 8q21-Q22
Rcc1-Like Domain and ORF15: Essentials in Rpgr Gene
Choroidal Neovascularization in Patients with Adult-Onset Foveomacular Dystrophy Caused by Mutations in the Rds/Peripherin Gene
Biochemical Characterisation of the C1QTNF5 Gene Associated With Late-Onset Retinal Degeneration. A Genetic Model of Age-Related Macular Degeneration
Bietti Crystalline Corneoretinal Dystrophy Associated with Cyp4v2 Gene Mutations
Fundus Appearance Of Choroideremia Using Optical Coherence Tomograpy
A2e, A Fluorophore Of Rpe Lipofuscin, Can Destabilie Membrane
Amino-Retinoid Compounds in The Human Retinal Pigment Epithelium
Annexins In Bruch’s Membrane and Drusen
Molecular Mechanisms of Photoreceptor Degeneration in RP Caused by Impdh1 Mutations.
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