Progression despite replacement of a myopathic form of coenzyme Q10 defect-Reference-Cited by-同舟云学术

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Progression despite replacement of a myopathic form of coenzyme Q10 defect

Published:2004-08-23 Issue:4 Volume:63 Page:727-729
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Aure K.,Benoist J. F.,de Baulny H. O.,Romero N. B.,Rigal O.,Lombes A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 74 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. Mitochondrial Dysfunction due to Novel COQ8A Variation with Poor Response to CoQ10 Treatment: A Comprehensive Study and Review of Literatures;The Cerebellum;2024-03-02

2. Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Hypomorphic variants and two distinct disease entities;Molecular Genetics and Metabolism;2023-08

3. COQ8A-Ataxia as a Manifestation of Primary Coenzyme Q Deficiency;Metabolites;2022-10-08

4. The efficacy of coenzyme Q ₁₀ treatment in alleviating the symptoms of primary coenzyme Q ₁₀ deficiency: A systematic review;Journal of Cellular and Molecular Medicine;2022-08-19

5. A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options;Molecular Genetics and Metabolism Reports;2022-06

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