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Results 1 - 10 of 32 for "Myopathy," "distal," 2
  1. Distal myopathy 2 is a condition characterized by weakness of specific muscles that begins in adulthood. It is a form of muscular dystrophy that specifically ...
  2. ... MATR3 gene has been identified in people with distal myopathy 2, a condition characterized by muscle and vocal cord weakness. The MATR3 gene mutation associated with distal myopathy 2 changes a single protein building block (amino acid) ...
  3. Muscular Dystrophy (National Library of Medicine)  
    What is muscular dystrophy (MD)? Muscular dystrophy (MD) is a group of more than 30 genetic diseases. They cause weakness of the muscles. Over time, the ...
  4. ... without rimmed vacuoles Distal myopathy with rimmed vacuoles Distal myopathy, Nonaka type DMRV Hereditary inclusion body myopathy type 2 HIBM2 IBM2 Inclusion body myopathy type 2 Inclusion ...
  5. ... caveolin-3 gene causes a peculiar form of distal myopathy. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2. ...
  6. ... caveolin-3 gene causes a peculiar form of distal myopathy. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2. ...
  7. ... I, Hayashi YK, Noguchi S. Molecular pathomechanism of distal myopathy with rimmed vacuoles. Acta Myol. 2005 Oct;24(2):80-3. Citation on PubMed Noguchi S, Keira ...
  8. ... Kozman H, Mastaglia FL, Kakulas BA. Autosomal dominant distal myopathy: linkage to chromosome 14. Am J Hum Genet. 1995 Feb;56(2):422-7. Citation on PubMed or Free article ...
  9. ... Citation on PubMed Udd B, Hackman P. Udd Distal Myopathy - Tibial Muscular Dystrophy. 2005 Feb 17 [updated 2020 Jan 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
  10. ... Romero N, Leturcq F, Eymard B. Miyoshi-like distal myopathy with mutations in anoctamin 5 gene. Rev Neurol (Paris). 2012 Feb;168(2):135-41. doi: 10.1016/j.neurol.2011. ...
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