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PUBMED FOR HANDHELDS

Journal Abstract Search


264 related items for PubMed ID: 15476279

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  • 2. Interleukin-1 expression in inflammatory myopathies: evidence of marked immunoreactivity in sarcoid granulomas and muscle fibres showing ischaemic and regenerative changes.
    Authier FJ, Mhiri C, Chazaud B, Christov C, Cherin P, Barlovatz-Meimon G, Gherardi RK.
    Neuropathol Appl Neurobiol; 1997 Apr; 23(2):132-40. PubMed ID: 9160898
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  • 3. [Inclusion body myositis and neuromuscular diseases with rimmed vacuoles].
    Figarella-Branger D, Pellissier JF, Pouget J, Calore EE, Azulay JP, Desnuelle C, Serratrice G.
    Rev Neurol (Paris); 1992 Apr; 148(4):281-90. PubMed ID: 1332175
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  • 4. A dual role for HSP90 and HSP70 in the inflammatory myopathies: from muscle fiber protection to active invasion by macrophages.
    De Paepe B, Creus KK, Martin JJ, Weis J, De Bleecker JL.
    Ann N Y Acad Sci; 2009 Sep; 1173():463-9. PubMed ID: 19758187
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  • 6. Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases.
    Olivé M, Goldfarb L, Dagvadorj A, Sambuughin N, Paulin D, Li Z, Goudeau B, Vicart P, Ferrer I.
    Acta Neuropathol; 2003 Jul; 106(1):1-7. PubMed ID: 12669240
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  • 12. Tau aggregates are abnormally phosphorylated in inclusion body myositis and have an immunoelectrophoretic profile distinct from other tauopathies.
    Maurage CA, Bussière T, Sergeant N, Ghesteem A, Figarella-Branger D, Ruchoux MM, Pellissier JF, Delacourte A.
    Neuropathol Appl Neurobiol; 2004 Dec; 30(6):624-34. PubMed ID: 15541003
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  • 13. Difference in adhesion molecule expression (ICAM-1 and VCAM-1) in juvenile and adult dermatomyositis, polymyositis and inclusion body myositis.
    Sallum AM, Kiss MH, Silva CA, Wakamatsu A, Vianna MA, Sachetti S, Marie SK.
    Autoimmun Rev; 2006 Feb; 5(2):93-100. PubMed ID: 16431335
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  • 15. The pathological diagnosis of specific inflammatory myopathies.
    Carpenter S, Karpati G.
    Brain Pathol; 1992 Jan; 2(1):13-9. PubMed ID: 1341942
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  • 16. Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.
    Neudecker S, Krasnianski M, Bahn E, Zierz S.
    Acta Neuropathol; 2004 Sep; 108(3):257-9. PubMed ID: 15221332
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  • 17. Oxidative stress and predominant Abeta42(43) deposition in myopathies with rimmed vacuoles.
    Tateyama M, Takeda A, Onodera Y, Matsuzaki M, Hasegawa T, Nunomura A, Hirai K, Perry G, Smith MA, Itoyama Y.
    Acta Neuropathol; 2003 Jun; 105(6):581-5. PubMed ID: 12734664
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  • 19. Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy.
    Sarkozi E, Askanas V, Engel WK.
    Am J Pathol; 1994 Dec; 145(6):1280-4. PubMed ID: 7992832
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