Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: Characterization of sub-clinical phenotypes-Reference-Cited by-同舟云学术

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Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: Characterization of sub-clinical phenotypes

Published:1994-07 Issue:4 Volume:4 Page:349-358
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Angelini C.,Fanin M.,Pegoraro E.,Freda M.P.,Cadaldini M.,Martinello F.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference39 articles.

1. Familial X-linked myalgia and cramps: a non progressive myopathy associated with a deletion in the dystrophin gene;Gospe;Neurology,1989

2. Early myocardial disease and cramping myalgia in Becker type muscular dystrophy: a kindred;Kuhn;Neurology,1979

3. Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy;Bushby;Hum Genet,1991

4. Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker muscular dystrophy;Doriguzzi;J Neurol,1993

5. Mild myopathic syndromes;Fischbeck,1991

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1. Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study;Journal of Neuromuscular Diseases;2024-03-05

2. Diverse Cardiac Phenotype of Becker Muscular Dystrophy: Under-Recognized Subclinical Cardiomyopathy Due to Partial Dystrophin Deficiency in a Contemporary Era;Pediatric Cardiology;2024-01-19

3. Clinical potential of microdystrophin as a surrogate endpoint;Neuromuscular Disorders;2023-01

4. Myalgic Becker Muscular Dystrophy Due to an Exon 15 Point Mutation: Case Series and Literature Review;Journal of Clinical Neuromuscular Disease;2022-12

5. Body composition and myokines in a cohort of patients with Becker muscular dystrophy;Muscle & Nerve;2022-05-27

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