A new congenital form of X-linked autophagic vacuolar myopathy-Reference-Cited by-同舟云学术

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A new congenital form of X-linked autophagic vacuolar myopathy

Published:2005-10-10 Issue:7 Volume:65 Page:1132-1134
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Yan C.,Tanaka M.,Sugie K.,Nobutoki T.,Woo M.,Murase N.,Higuchi Y.,Noguchi S.,Nonaka I.,Hayashi Y. K.,Nishino I.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 27 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. Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis;Human Molecular Genetics;2023-09-26

2. Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant;Neuromuscular Disorders;2023-07

3. X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in Children;Neurology India;2022

4. Autophagy dysfunction in skeletal myopathies: Inclusion body myositis and Danon disease;Autophagy Dysfunction in Alzheimer's Disease and Dementia;2022

5. Autophagic vacuolar myopathy: Danon disease and related myopathies;Neurology and Clinical Neuroscience;2021-10-06

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