Dysferlin deficiency treated like refractory polymyositis-Reference-Cited by-同舟云学术

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Dysferlin deficiency treated like refractory polymyositis

Published:2009-09-04 Issue:1 Volume:29 Page:
ISSN:0770-3198
Container-title:Clinical Rheumatology
language:en
Short-container-title:Clin Rheumatol

Author:

Vinit Julien,Samson Maxime,Gaultier Jean-Baptiste,Laquerriere Annie,Ollagnon Elisabeth,Petiot Philippe,Marie Isabelle,Levesque Hervé,Rousset Hugues

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Rheumatology

Link

http://link.springer.com/content/pdf/10.1007/s10067-009-1273-1.pdf

Reference8 articles.

1. Ueyama H, Kumamoto T, Horinouchi H, Fujimoto S, Aono H, Tsuda T (2002) Clinical heterogeneity in dysferlinopathy. Intern Med 41:532–536

2. Guglieri M, Magri F, D'Angelo MG, Prelle A, Morandi L, Rodolico C et al (2008) Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients. Hum Mutat 29:258–266

3. Nguyen K, Bassez G, Krahn M, Bernard R, Laforet P, Labelle V et al (2007) Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes. Arch Neurol 64:1176–1182

4. Dincer P, Akcoren Z, Demir E, Richard I, Sancak O, Kale G et al (2000) A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. J Med Genet 37:361–367

5. Confalonieri P, Oliva L, Andreetta F, Lorenzoni R, Dassi P, Mariani E et al (2003) Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study. J Neuroimmunol 142:130–136

Cited by 17 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. Limb girdle muscular dystrophies;Česká a slovenská neurologie a neurochirurgie;2022-12-31

2. Reasons for misdiagnosis of polymyositis in patients with dysferlinopathy: a clinical case;Neuromuscular Diseases;2022-12-13

3. Dysferlinopathy misdiagnosed with juvenile polymyositis in the pre-symptomatic stage of hyperCKemia: a case report and literature review;BMC Medical Genomics;2022-06-20

4. Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi Arabia;Frontiers in Neuroscience;2022-02-22

5. A Patient With Late-onset Limb-girdle Muscular Dystrophy Type 2B Mimicking Dermatomyositis: A Case Report and Review;Journal of Rheumatic Diseases;2021-04-01

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