Atlas of Inherited Retinal Diseases
portes grátis
Atlas of Inherited Retinal Diseases
Diaconita, Vlad; Tsang, Stephen H.; Sharma, Tarun
Springer International Publishing AG
12/2024
300
Dura
9783031722295
Pré-lançamento - envio 15 a 20 dias após a sua edição
Descrição não disponível.
Chapter 1 Retinal Histology and Anatomical Landmarks.- Chapter 2 Fluorescein Angiography.- Chapter 3 Optical Coherence Tomography.- Chapter 4 Fundus Autofluorescence.- Chapter 5 ERG.- Chapter 6 Electrooculography.- Chapter 7 Glossary of Relevant Genetic and MolecularCell Biology.- Chapter 8 X-linked Retinitis Pigmentosa.- Chapter 9 X-linked Choroideremia.- Chapter 10 X-linked Juvenile Retinoschisis.- Chapter 11 X-linked Ocular Albinism.- Chapter 12 Progressive Cone Dystrophy and Cone-Rod Dystrophy.- Chapter 13 Congenital Stationary Night Blindness.- Chapter 14 Blue Cone Monochromatism.- Chapter 15 Autosomal Dominant Retinitis Pigmentosa.- Chapter 16 Best Vitelliform Macular Dystrophy.- Chapter 17 Pattern Dystrophy.- Chapter 18 Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese, Autosomal Dominant Drusen).- Chapter 19 Occult Macular Dystrophy.- Chapter 20 Sorsby Pseudoinflammatory Fundus Dystrophy.- Chapter 21 North Carolina Macular Dystrophy.- Chapter 22 Pigmented Paravenous Chorioretinal Atrophy (PPCRA).- Chapter 23 Late-Onset Retinal Degeneration.- Chapter 24 Achromatopsia (Rod Monochromatism).- Chapter 25 Retinitis Pigmentosa (Non-syndromic).- Chapter 26 Leber Congenital Amaurosis.- Chapter 27 Stargardt Disease.- Chapter 28 Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome).- Chapter 29 Best Vitelliform Macular Dystrophy.- Chapter 30 Mitochondrial Disorder Kearns-Sayre Syndrome.- Chapter 31 MIDD.- Chapter 32 Usher Syndrome.- Chapter 33 Bardet-Biedl Syndrome.- Chapter 34 Senior-Loken Syndrome.- Chapter 35 Alstrom Syndrome. Chapter 36 Sjogren-Larsson Syndrome.- Chapter 37 Inborn Errors of Metabolism Gyrate Atrophy.- Chapter 38 Pseudoxanthoma Elasticum.- Chapter 39 Refsum Disease.- Chapter 40 Bietti.- Chapter 41 Alport Syndrome.- Chapter 42 N - Stickler Syndrome.- Chapter 43 N - OTX2 Syndrome.- Chapter 44 VHL.- Chapter 45 Tuberous Sclerosis.- Chapter 46 Neurofibromatosis.- Chapter 47 Rubella Retinopathy.- Chapter 48 Syphilis.- Chapter 49 AIR.- Chapter 50 Drug-Induced Retinal Toxicity.- Chapter 51 Non-Infectious Uveitis.- Chapter 52 Diffuse Unilateral Subacute Neuroretinitis (DUSN).- Chapter 53 CSCR.- Chapter 54 Pathologic Myopia.- Chapter 55 A Practical Approach to Retinal Dystrophies.- Chapter 56 Genetic Testing For Inherited Retinal Dystrophy.- Chapter 57 Genetic Reports.- Chapter 58 The genetic basis of IRDS and the role of genetic testing.- Chapter 59 Seeing Stars The Gene Therapy Revolution.- Chapter 60 Mutation Specific Treatments for Inherited Retinal Diseases.- Chapter 61 Global Treatment Approaches Part 1 Neuroprotection and Stem Cell Therapy.- Chapter 62 Global Treatment Approaches Part 2 Optogenetics and Retinal Implants.
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genetic eye disorder;molecular genetics;genome testing;exon sequencing;gene therapy
Chapter 1 Retinal Histology and Anatomical Landmarks.- Chapter 2 Fluorescein Angiography.- Chapter 3 Optical Coherence Tomography.- Chapter 4 Fundus Autofluorescence.- Chapter 5 ERG.- Chapter 6 Electrooculography.- Chapter 7 Glossary of Relevant Genetic and MolecularCell Biology.- Chapter 8 X-linked Retinitis Pigmentosa.- Chapter 9 X-linked Choroideremia.- Chapter 10 X-linked Juvenile Retinoschisis.- Chapter 11 X-linked Ocular Albinism.- Chapter 12 Progressive Cone Dystrophy and Cone-Rod Dystrophy.- Chapter 13 Congenital Stationary Night Blindness.- Chapter 14 Blue Cone Monochromatism.- Chapter 15 Autosomal Dominant Retinitis Pigmentosa.- Chapter 16 Best Vitelliform Macular Dystrophy.- Chapter 17 Pattern Dystrophy.- Chapter 18 Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese, Autosomal Dominant Drusen).- Chapter 19 Occult Macular Dystrophy.- Chapter 20 Sorsby Pseudoinflammatory Fundus Dystrophy.- Chapter 21 North Carolina Macular Dystrophy.- Chapter 22 Pigmented Paravenous Chorioretinal Atrophy (PPCRA).- Chapter 23 Late-Onset Retinal Degeneration.- Chapter 24 Achromatopsia (Rod Monochromatism).- Chapter 25 Retinitis Pigmentosa (Non-syndromic).- Chapter 26 Leber Congenital Amaurosis.- Chapter 27 Stargardt Disease.- Chapter 28 Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome).- Chapter 29 Best Vitelliform Macular Dystrophy.- Chapter 30 Mitochondrial Disorder Kearns-Sayre Syndrome.- Chapter 31 MIDD.- Chapter 32 Usher Syndrome.- Chapter 33 Bardet-Biedl Syndrome.- Chapter 34 Senior-Loken Syndrome.- Chapter 35 Alstrom Syndrome. Chapter 36 Sjogren-Larsson Syndrome.- Chapter 37 Inborn Errors of Metabolism Gyrate Atrophy.- Chapter 38 Pseudoxanthoma Elasticum.- Chapter 39 Refsum Disease.- Chapter 40 Bietti.- Chapter 41 Alport Syndrome.- Chapter 42 N - Stickler Syndrome.- Chapter 43 N - OTX2 Syndrome.- Chapter 44 VHL.- Chapter 45 Tuberous Sclerosis.- Chapter 46 Neurofibromatosis.- Chapter 47 Rubella Retinopathy.- Chapter 48 Syphilis.- Chapter 49 AIR.- Chapter 50 Drug-Induced Retinal Toxicity.- Chapter 51 Non-Infectious Uveitis.- Chapter 52 Diffuse Unilateral Subacute Neuroretinitis (DUSN).- Chapter 53 CSCR.- Chapter 54 Pathologic Myopia.- Chapter 55 A Practical Approach to Retinal Dystrophies.- Chapter 56 Genetic Testing For Inherited Retinal Dystrophy.- Chapter 57 Genetic Reports.- Chapter 58 The genetic basis of IRDS and the role of genetic testing.- Chapter 59 Seeing Stars The Gene Therapy Revolution.- Chapter 60 Mutation Specific Treatments for Inherited Retinal Diseases.- Chapter 61 Global Treatment Approaches Part 1 Neuroprotection and Stem Cell Therapy.- Chapter 62 Global Treatment Approaches Part 2 Optogenetics and Retinal Implants.
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
