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Journal Abstract Search

257 related items for PubMed ID: 11556002

  • 1. [Fukuyama type congenital muscular dystrophy].
    Osawa M, Hino N.
    Ryoikibetsu Shokogun Shirizu; 2001; (35):97-102. PubMed ID: 11556002
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  • 7. Cardiac involvement in Fukuyama-type congenital muscular dystrophy.
    Nakanishi T, Sakauchi M, Kaneda Y, Tomimatsu H, Saito K, Nakazawa M, Osawa M.
    Pediatrics; 2006 Jun; 117(6):e1187-92. PubMed ID: 16717122
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  • 8. Seizure-genotype relationship in Fukuyama-type congenital muscular dystrophy.
    Yoshioka M, Higuchi Y, Fujii T, Aiba H, Toda T.
    Brain Dev; 2008 Jan; 30(1):59-67. PubMed ID: 17597323
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  • 9. POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease.
    Diesen C, Saarinen A, Pihko H, Rosenlew C, Cormand B, Dobyns WB, Dieguez J, Valanne L, Joensuu T, Lehesjoki AE.
    J Med Genet; 2004 Oct; 41(10):e115. PubMed ID: 15466003
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  • 10. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
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  • 11. [Fukuyama-type congenital muscular dystrophy and alpha-dystroglycanopathy].
    Kobayashi K, Toda T.
    Tanpakushitsu Kakusan Koso; 2004 Nov 07; 49(15 Suppl):2457-62. PubMed ID: 15553001
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  • 18. [Muscular dystrophy, congenital with mental retardation, Fukuyama type].
    Saito K.
    Ryoikibetsu Shokogun Shirizu; 2001 Nov 07; (34 Pt 2):225-7. PubMed ID: 11528712
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  • 19. Diagnosis and etiology of congenital muscular dystrophy.
    Peat RA, Smith JM, Compton AG, Baker NL, Pace RA, Burkin DJ, Kaufman SJ, Lamandé SR, North KN.
    Neurology; 2008 Jul 29; 71(5):312-21. PubMed ID: 18160674
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