Muscular dystrophy [NEW TOPIC PAGE]

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From CDC-Authored Genomics Publication Database

This database contains CDC-authored publications in public health genomics including infectious diseases, newborn screening, reproductive health, genetic testing, cancer, chronic diseases, birth defects and developmental disabilities, environmental and occupational health as well as laboratory, bioinformatics and statistical methods.

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• Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management.
  Birnkrant David J et al. The Lancet. Neurology 2018 Jan
• Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.
  Birnkrant David J et al. The Lancet. Neurology 2018 Jan
• Prevalence of Duchenne and Becker muscular dystrophies in the United States.
  Romitti Paul A et al. Pediatrics 2015 Mar 135(3) 513-21
• Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing.
  Kalman Lisa et al. J Mol Diagn 2013 Jul 15(4) 518-25
• Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy.
  Nabukera Sarah K et al. Am. J. Med. Genet. A 2013 Jan 161A(1) 70-5
• Evidence-based path to newborn screening for Duchenne muscular dystrophy.
  Mendell Jerry R et al. Ann. Neurol. 2012 Mar 71(3) 304-13

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