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PUBMED FOR HANDHELDS

Journal Abstract Search


165 related items for PubMed ID: 1850594

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Inclusion body myositis.
    Chou SM.
    Baillieres Clin Neurol; 1993 Nov; 2(3):557-77. PubMed ID: 8156143
    [Abstract] [Full Text] [Related]

  • 23. [Inclusion body myositis: clinical and myopathological features].
    Xie H, Wang L, Shen D.
    Zhonghua Nei Ke Za Zhi; 1997 Sep; 36(9):610-2. PubMed ID: 10436972
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. [Clinical forms of inclusion body myositis: 12 cases].
    Serratrice G, Pellissier JF, Pouget J, Figarella-Branger D.
    Rev Neurol (Paris); 1989 Sep; 145(11):781-8. PubMed ID: 2556772
    [Abstract] [Full Text] [Related]

  • 26. Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndrome.
    Cole AJ, Kuzniecky R, Karpati G, Carpenter S, Andermann E, Andermann F.
    Brain; 1988 Oct; 111 ( Pt 5)():1025-37. PubMed ID: 2846114
    [Abstract] [Full Text] [Related]

  • 27. Inclusion body myositis (IBM): myopathy or neuropathy?
    Eisen A, Berry K, Gibson G.
    Neurology; 1983 Sep; 33(9):1109-14. PubMed ID: 6310442
    [Abstract] [Full Text] [Related]

  • 28. Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
    Argov Z, Tiram E, Eisenberg I, Sadeh M, Seidman CE, Seidman JG, Karpati G, Mitrani-Rosenbaum S.
    Ann Neurol; 1997 Apr; 41(4):548-51. PubMed ID: 9124813
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  • 29.
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  • 30.
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  • 31.
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  • 32. Inclusion body myositis: a chronic persistent mumps myositis?
    Chou SM.
    Hum Pathol; 1986 Aug; 17(8):765-77. PubMed ID: 3015764
    [Abstract] [Full Text] [Related]

  • 33. Idiopathic inflammatory myopathies: inclusion-body myositis, polymyositis, and dermatomyositis.
    Askanas V, Engel WK, Mirabella M.
    Curr Opin Neurol; 1994 Oct; 7(5):448-56. PubMed ID: 7804466
    [Abstract] [Full Text] [Related]

  • 34. Inclusion body myositis in French patients. A clinicopathological evaluation.
    Mhiri C, Gherardi R.
    Neuropathol Appl Neurobiol; 1990 Aug; 16(4):333-44. PubMed ID: 2172855
    [Abstract] [Full Text] [Related]

  • 35. Dysphagia in inclusion body myositis.
    Wintzen AR, Bots GT, de Bakker HM, Hulshof JH, Padberg GW.
    J Neurol Neurosurg Psychiatry; 1988 Dec; 51(12):1542-5. PubMed ID: 2851642
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. Fast and reliable new method for electron-microscopic identification of cytoplasmic tubulo-filaments in muscle biopsies of patients with inclusion-body myositis.
    Askanas V, Alvarez RB.
    Acta Neuropathol; 1992 Dec; 84(3):335-6. PubMed ID: 1329431
    [No Abstract] [Full Text] [Related]

  • 38.
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  • 39. The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
    Eisenberg I, Avidan N, Potikha T, Hochner H, Chen M, Olender T, Barash M, Shemesh M, Sadeh M, Grabov-Nardini G, Shmilevich I, Friedmann A, Karpati G, Bradley WG, Baumbach L, Lancet D, Asher EB, Beckmann JS, Argov Z, Mitrani-Rosenbaum S.
    Nat Genet; 2001 Sep; 29(1):83-7. PubMed ID: 11528398
    [Abstract] [Full Text] [Related]

  • 40. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy.
    Askanas V, Serdaroglu P, Engel WK, Alvarez RB.
    Neurosci Lett; 1991 Sep 02; 130(1):73-6. PubMed ID: 1660975
    [Abstract] [Full Text] [Related]


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