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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 6311038

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  • 4. A benign form of reducing body myopathy.
    Oh SJ, Meyers GJ, Wilson ER, Alexander CB.
    Muscle Nerve; 1983 May; 6(4):278-82. PubMed ID: 6306460
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  • 5. Transient cytoplasmic bodies in muscle of three infants with Werdnig-Hoffmann disease.
    Buchino JJ, Bove KE, Iannaccone ST.
    Pediatr Pathol; 1990 May; 10(4):563-73. PubMed ID: 2164661
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  • 6. Congenital myopathy with cytoplasmic bodies.
    Goebel HH, Schloon H, Lenard HG.
    Neuropediatrics; 1981 May; 12(2):166-80. PubMed ID: 6267501
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  • 11. [A clinical, histochemical and ultrastructural study of mitochondrial myopathy].
    Jiang XM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Oct; 23(5):297-9, 320. PubMed ID: 2178086
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  • 12. Centronuclear myopathy with type I fibre hypotrophy and "fingerprint" inclusions associated with Marfan's syndrome.
    Jadro-Santel D, Grcević N, Dogan S, Franjić J, Benc H.
    J Neurol Sci; 1980 Feb; 45(1):43-56. PubMed ID: 6244371
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  • 15. Adult polyglucosan body myopathy.
    Goebel HH, Shin YS, Gullotta F, Yokota T, Alroy J, Voit T, Haller P, Schulz A.
    J Neuropathol Exp Neurol; 1992 Jan; 51(1):24-35. PubMed ID: 1311021
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  • 17. A fluorescent microscopy study of biopsied muscles from infantile neuromuscular disorders.
    Miike T, Tamari H, Ohtani Y, Nakamura H, Matsuda I, Miyoshino S.
    Acta Neuropathol; 1983 Jan; 59(1):48-52. PubMed ID: 6837268
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  • 18. Inclusion body myositis in post-poliomyelitis muscular atrophy.
    Abarbanel JM, Lichtenfeld Y, Zirkin H, Louzon Z, Osimani A, Farkash P, Herishanu Y.
    Acta Neurol Scand; 1988 Aug; 78(2):81-4. PubMed ID: 2845701
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  • 19. Type II fiber myolysis in a patient with hypocarnitinemia.
    Kimura S, Miyake S.
    Brain Dev; 1989 Aug; 11(4):263-5. PubMed ID: 2774097
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