Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies-Reference-Cited by-同舟云学术

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Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies

Published:2010-06-23 Issue:4 Volume:75 Page:316-323
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Paradas C.,Llauger J.,Diaz-Manera J.,Rojas-Garcia R.,De Luna N.,Iturriaga C.,Marquez C.,Uson M.,Hankiewicz K.,Gallardo E.,Illa I.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 108 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

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2. Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study;Journal of Neurology;2024-07-07

3. The Dysferlinopathies Conundrum: Clinical Spectra, Disease Mechanism and Genetic Approaches for Treatments;Biomolecules;2024-02-21

4. Magnetic resonance imaging-based criteria to differentiate dysferlinopathy from other genetic muscle diseases;Neuromuscular Disorders;2024-01

5. Patterns of Clinical Progression Among Patients With Autosomal Recessive Limb-Girdle Muscular Dystrophy: A Systematic Review;Journal of Clinical Neuromuscular Disease;2023-12

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