Expanding sialidosis spectrum by genome-wide screening: NEU1 mutations in adult-onset myoclonus-Reference-Cited by-同舟云学术

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

Published:2014-05-07 Issue:22 Volume:82 Page:2003-2006
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Canafoglia L.,Robbiano A.,Pareyson D.,Panzica F.,Nanetti L.,Giovagnoli A. R.,Venerando A.,Gellera C.,Franceschetti S.,Zara F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 40 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. Clinical and Structural Characteristics of NEU1 Variants Causing Sialidosis Type 1;Journal of Movement Disorders;2024-07-31

2. 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

3. Sialidosis type 1 without cherry-red spots: a case report and literature review;BMJ Neurology Open;2024-02

4. Myoclonus;Movement Disorders Phenomenology;2024

5. Adult-Onset Genetic Leukoencephalopathies With Movement Disorders;Journal of Movement Disorders;2023-05-31

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