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Hereditary Chorioretinal Disorders

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Autore: Cheung
Editore: Springer
Anno: 2020
Pagine: 181
ISBN: 9789811504136
Prezzo: 200,00€
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This volume of the retina atlas focuses on hereditary chorioretinal disorders. The topics covered include retinitis pigmentosa, Best disease, congenital X-linked retinoschisis, cone dystrophy, Stargardt’s disease, pattern dystrophy, North Carolina macular dystrophy, choroideremia, Mallattia Leventinese, Bietti’s crystalline dystrophy, and albinism. All clinical features are clearly illustrated with multimodal imaging techniques. The utility of some of the latest imaging tools such as OCT angiography, adaptive optics-scanning laser ophthalmoscopy, and microperimetery is discussed. Readers will gain valuable new insights into pathogenesis at the molecular level, which have been facilitated by recent genetic discoveries. The use of genetic testing and the latest advances in and challenges of gene therapy and cell-based therapy are also covered in detail.
Hereditary Chorioretinal Disorders atlas is one of nine volumes in the series Retina Atlas. The series provides validated and comprehensive information on vitreoretinal diseases, covering imaging basics, retinal vascular diseases, macular disorders, ocular inflammatory and infectious disorders, retinal degeneration, the surgical retina, ocular oncology, pediatric retina and trauma.

  • Retinitis Pigmentosa

    Pages 1-43

    Chou, Hung-Da (et al.)

  • Pages 45-50

    Putri, Christine Anggun (et al.)

  • X-Linked Retinoschisis

    Pages 51-66

    Kang, Eugene Yu-Chuan (et al.)

  • Progressive Cone/Cone-Rod Dystrophy

    Pages 67-74

    Tsai, Andrew (et al.)

  • Pattern Dystrophy

    Pages 75-84

    Tsai, Andrew (et al.)

  • Stargardt Macular Dystrophy

    Pages 85-94

    Vaclavik, Veronika

  • North Carolina Macular Dystrophy

    Pages 95-98

    Small, Leslie (et al.)

  • Choroideremia

    Pages 99-106

    MacDonald, Ian M. (et al.)

  • Malattia Leventinese

    Pages 107-117

    Vaclavik, Veronika

  • Bietti’s Crystalline Dystrophy

    Pages 119-138

    Kang, Eugene Yu-Chuan (et al.)

  • Albinism

    Pages 139-147

    Choi, Jessy (et al.)

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