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Titlebook: Inherited Retinal Disease; Hyeong-Gon Yu Book 2022 Springer Nature Singapore Pte Ltd. 2022 Inherited retinal disease.retinitis pigmentosa.

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發(fā)表于 2025-3-21 16:21:05 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Inherited Retinal Disease
編輯Hyeong-Gon Yu
視頻videohttp://file.papertrans.cn/467/466466/466466.mp4
概述Updates on clinical features and molecular diagnosis.Cases contributed by global leaders in the field.Clinical photographs obtained with newer imaging techniques.Many images of rare but clinically imp
圖書封面Titlebook: Inherited Retinal Disease;  Hyeong-Gon Yu Book 2022 Springer Nature Singapore Pte Ltd. 2022 Inherited retinal disease.retinitis pigmentosa.
描述This book presents the latest knowledge and expert guidance on all aspects of inherited retinal diseases, including molecular genetics, diagnosis, clinical features, general principles of treatment, novel treatment methods, and genetic counseling. Recent years have witnessed great advances in understanding of the genetic and cytological background of these diseases. Genetic analysis methods such as next generation sequencing have remarkably reduced the cost and time required for massive analysis of patients’ samples. Studies on gene therapy and stem cell therapy have been successfully carried out in animal models, and gene therapy is now available for Leber congenital amaurosis caused by RPE65 mutations. Against this background, Inherited Retinal Disease will be an invaluable up-to-date resource for ophthalmologists, medical students, and researchers in ocular inflammation. In addition to supplying essential information on each individual disorder, it features many interesting cases contributed by global leaders in the field as well as clinical photographs obtained with newer imaging techniques and numerous images of rare but clinically important diseases.
出版日期Book 2022
關鍵詞Inherited retinal disease; retinitis pigmentosa; retinal dystrophy; genetic diagnosis; molecular genetic
版次1
doihttps://doi.org/10.1007/978-981-16-7337-5
isbn_softcover978-981-16-7339-9
isbn_ebook978-981-16-7337-5
copyrightSpringer Nature Singapore Pte Ltd. 2022
The information of publication is updating

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g cases contributed by global leaders in the field as well as clinical photographs obtained with newer imaging techniques and numerous images of rare but clinically important diseases.978-981-16-7339-9978-981-16-7337-5
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Kaoru Fujinami,Yu Fujinami-Yokokawa,Lizhu Yang,Xiao Liu,Gavin Arno,Nikolas Pontikos,East Asia Inheri
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Vitelliform Macular Dystrophy,n the diagnosis of VMD because the clinical features of VMD are similar to those of exudative age-related macular degeneration (AMD), choroidal neovascularization (CNV), or central serous chorioretinopathy (CSC). Here, in addition to describing the clinical characteristics of VMD, this chapter focuses on the clinical genetics of . gene in VMD.
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