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Results 1 - 10 of 14 for Inclusion body myopathy 3
  1. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... Kimonis VE. Global gene profiling of VCP-associated inclusion body myopathy. Clin Transl Sci. 2012 Jun;5(3):226-34. doi: 10.1111/j.1752-8062.2012.00407.x. Epub 2012 Apr 4. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  2. VCP gene 
    ... multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. J Mol Neurosci. 2011 Nov;45(3):522-31. doi: 10.1007/s12031-011-9627- ...
    https://medlineplus.gov/genetics/gene/vcp - Genetics
  3. GNE myopathy 
    ... on distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy: contributions from an animal model. Lack of sialic acid, a central determinant in sugar chains, causes myopathy? Acta Myol. 2007 Dec;26(3):171-5. Citation on PubMed or Free article ...
    https://medlineplus.gov/genetics/condition/gne-myopathy - Genetics
  4. SELENON gene 
    ... and insulin resistance. Ann Neurol. 2006 Mar;59(3):546-52. doi: ... Mallory body-like inclusions is caused by mutations of the selenoprotein N ...
    https://medlineplus.gov/genetics/gene/selenon - Genetics
  5. GNE gene 
    ... Wirguin I, Soffer D, Mitrani-Rosenbaum S. Hereditary inclusion body myopathy: the Middle Eastern genetic cluster. Neurology. 2003 May ... acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. Nat Genet. 2001 Sep;29(1):83-7. ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  6. Find a Neuromuscular Disease (Muscular Dystrophy Association)  
    Neuromuscular Disorders/Start Here ... Neuromuscular Disorders ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy ...
    https://www.mda.org/disease/list - External Health Links
  7. Myosin storage myopathy 
    ... mutation in myosin storage myopathy and scapulo-peroneal myopathy. Neuromuscul Disord. ... Acta Neuropathol. 2013 Jan;125(1):3-18. doi: 10.1007/s00401-012-1024-2. ...
    https://medlineplus.gov/genetics/condition/myosin-storage-myopathy - Genetics
  8. Idiopathic inflammatory myopathy 
    ... Genetic Testing Registry: Myositis disease Genetic Testing Registry: Inclusion body myositis Idiopathic inflammatory myopathy National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../idiopathic-inflammatory-myopathy - Genetics
  9. Rigid spine muscular dystrophy 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov CONGENITAL MYOPATHY 3 WITH RIGID SPINE; CMYP3 PubMed Ardissone A, Bragato ... Morandi L, Mora M, Moroni I. SEPN1-related myopathy in three patients: novel mutations and diagnostic clues. Eur J ...
    https://medlineplus.gov/.../condition/rigid-spine-muscular-dystrophy - Genetics
  10. Inclusion-Body Myositis: Diagnosis (Muscular Dystrophy Association)  
    Myositis/Diagnosis and Tests ... Myositis ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy for people living ...
    https://www.mda.org/disease/inclusion-body-myositis/diagnosis - External Health Links
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