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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 10417791

  • 1.
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  • 2. Localization of dystrophin and beta-spectrin in vacuolar myopathies.
    De Bleecker JL, Engel AG, Winkelmann JC.
    Am J Pathol; 1993 Oct; 143(4):1200-8. PubMed ID: 8214011
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  • 3. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies.
    Jones KJ, Kim SS, North KN.
    J Med Genet; 1998 May; 35(5):379-86. PubMed ID: 9610800
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  • 4. Autophagic vacuolar myopathy in twin girls.
    Holton JL, Beesley C, Jackson M, Venner K, Bhardwaj N, Winchester B, Al-Memar A.
    Neuropathol Appl Neurobiol; 2006 Jun; 32(3):253-9. PubMed ID: 16640643
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  • 5. Caveolin-3 is not an integral component of the dystrophin glycoprotein complex.
    Crosbie RH, Yamada H, Venzke DP, Lisanti MP, Campbell KP.
    FEBS Lett; 1998 May 08; 427(2):279-82. PubMed ID: 9607328
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  • 7. Immunogold localization of adhalin, alpha-dystroglycan and laminin in normal and dystrophic skeletal muscle.
    Cullen MJ, Walsh J, Roberds SL, Campbell KP.
    Biochem Soc Trans; 1996 May 08; 24(2):274S. PubMed ID: 8736932
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  • 9. Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter.
    Echenne B, Rivier F, Jellali AJ, Azais M, Mornet D, Pons F.
    Neuromuscul Disord; 1997 May 08; 7(3):187-90. PubMed ID: 9185183
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  • 12. Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities.
    Mora M, Moroni I, Uziel G, di Blasi C, Barresi R, Farina L, Morandi L.
    Neuromuscul Disord; 1996 Oct 08; 6(5):377-81. PubMed ID: 8938702
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  • 13. Fukuyama-type congenital muscular dystrophy: close relation between changes in the muscle basal lamina and plasma membrane.
    Matsubara S, Mizuno Y, Kitaguchi T, Isozaki E, Miyamoto K, Hirai S.
    Neuromuscul Disord; 1999 Oct 08; 9(6-7):388-98. PubMed ID: 10545042
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  • 15. Multiplex Western blotting system for the analysis of muscular dystrophy proteins.
    Anderson LV, Davison K.
    Am J Pathol; 1999 Apr 08; 154(4):1017-22. PubMed ID: 10233840
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  • 18. Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study.
    ter Laak HJ, Leyten QH, Gabreëls FJ, Kuppen H, Renier WO, Sengers RC.
    Clin Neurol Neurosurg; 1998 Mar 08; 100(1):5-10. PubMed ID: 9637197
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  • 19. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects.
    Handa V, Mital A, Gupta M, Goyle S.
    Neurol India; 2001 Mar 08; 49(1):19-24. PubMed ID: 11303236
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  • 20. Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy.
    Murakami N, Goto Y, Itoh M, Katsumi Y, Wada T, Ozawa E, Nonaka I.
    Neuromuscul Disord; 1995 Mar 08; 5(2):149-55. PubMed ID: 7539316
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