| 書(shū)目名稱 | Hereditary Chorioretinal Disorders | | 編輯 | Gemmy Cheung | | 視頻video | http://file.papertrans.cn/426/425839/425839.mp4 | | 概述 | Provides clearly illustrated examples of various clinical manifestations.Covers the latest advances in our understanding of their genetic background and pathophysiology.Includes findings with the late | | 叢書(shū)名稱 | Retina Atlas | | 圖書(shū)封面 |  | | 描述 | .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 retin | | 出版日期 | Book 2020 | | 關(guān)鍵詞 | Retinitis Pigmentosa; Best‘s Disease; Congenital X-linked Retinoschisis; Cone Dystrophy; North Carolina | | 版次 | 1 | | doi | https://doi.org/10.1007/978-981-15-0414-3 | | isbn_softcover | 978-981-15-0416-7 | | isbn_ebook | 978-981-15-0414-3Series ISSN 2662-5741 Series E-ISSN 2662-575X | | issn_series | 2662-5741 | | copyright | Springer Nature Singapore Pte Ltd. 2020 |
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