Sialidosis Type I without a Cherry Red Spot— Is There a Genetic Basis?-Reference-Cited by-同舟云学术

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Sialidosis Type I without a Cherry Red Spot— Is There a Genetic Basis?

Published:2021-01-31 Issue:1 Volume:14 Page:65-69
ISSN:2005-940X
Container-title:Journal of Movement Disorders
language:en
Short-container-title:JMD

Author:

Neeraja Koti,Holla Vikram Venkappayya,Prasad Shweta,Surisetti Bharath Kumar,Rakesh Kempaiah,Kamble Nitish,Yadav Ravi,Pal Pramod Kumar

Publisher

The Korean Movement Disorder Society

Subject

Clinical Neurology,Neurology

Link

http://e-jmd.org/upload/jmd-20083.pdf

Reference10 articles.

1. Sialidosis: A Review of Morphology and Molecular Biology of a Rare Pediatric Disorder

2. Expanding sialidosis spectrum by genome-wide screening: NEU1 mutations in adult-onset myoclonus

3. A longitudinal study of Taiwanese Sialidosis type 1: an insight into the concept of cherry-red spot myoclonus syndrome

4. Sialidosis Type 1 Without Cherry-Red Spot

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unique clinical and electrophysiological features in the peripheral nerve system in patients with sialidosis – a case series study;Orphanet Journal of Rare Diseases;2024-05-24

2. A fuzzy rule based machine intelligence model for cherry red spot disease detection of human eyes in IoMT;Wireless Networks;2022-09-10

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