Early diagnosis in Duchenne muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Failure of early diagnosis in symptomatic Duchenne muscular dystrophy;Bushby;Lancet,1999
2. Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity;Cox;Nature,1993
3. Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice;Ragot;Nature,1993
4. Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoplast transplantation;Gussoni;Nature,1992
5. Myoblast transfer in the treatment of Duchenne's dystrophy;Mendell;N Engl J Med,1995
Cited by 7 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. Clinical and Molecular Diagnosis in Muscular Dystrophies;Muscular Dystrophies;2019-10-02
2. Natural history of a cohort of Duchenne muscular dystrophy children seen between 1998 and 2014: An observational study from South India;Neurology India;2018
3. A mixed methods study of age at diagnosis and diagnostic odyssey for Duchenne muscular dystrophy;European Journal of Human Genetics;2015-01-28
4. Dystrophinopathies;Neuromuscular Disorders of Infancy, Childhood, and Adolescence;2015
5. Delayed Diagnosis in Duchenne Muscular Dystrophy: Data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet);The Journal of Pediatrics;2009-09
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