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Journal Abstract Search

80 related items for PubMed ID: 3665271

  • 1. [Fukuyama type congenital muscular dystrophy (FCMD) with a long survival--an autopsy case report].
    Ohtake T, Nagashima T, Tanabe H, Oda M, Satoh J.
    Rinsho Shinkeigaku; 1987 Jun; 27(6):767-74. PubMed ID: 3665271
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  • 2. Autopsy analyses of the muscular dystrophies.
    Moriuchi T, Kagawa N, Mukoyama M, Hizawa K.
    Tokushima J Exp Med; 1993 Jun; 40(1-2):83-93. PubMed ID: 8211986
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  • 8. Prenatal diagnosis of Fukuyama type congenital muscular dystrophy by polymorphism analysis.
    Kondo E, Saito K, Toda T, Osawa M, Yamamoto T, Kobayashi M, Fukuyama Y.
    Am J Med Genet; 1996 Dec 11; 66(2):169-74. PubMed ID: 8958324
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  • 9. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain.
    Saito Y, Mizuguchi M, Oka A, Takashima S.
    Ann Neurol; 2000 Jun 11; 47(6):756-64. PubMed ID: 10852541
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  • 10. [A case of Duchenne type of progessive muscular dystrophy verified by postmortem examination].
    Jedrzejowska-Kulakowska, Hausmanowa-Petrusewicz I, Gawlik Z, Rafalowska J, Slucka C.
    Neuropatol Pol; 1968 Jun 11; 6(1):71-85. PubMed ID: 5665043
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  • 12. Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.
    Toda T, Watanabe T, Matsumura K, Sunada Y, Yamada H, Nakano I, Mannen T, Kanazawa I, Shimizu T.
    Muscle Nerve; 1995 May 11; 18(5):508-17. PubMed ID: 7739638
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  • 16. An electron microscopical study of the T-system in biopsied muscles from Fukuyama type congenital muscular dystrophy.
    Miike T, Ohtani Y, Tamari H, Ishitsu T, Nonaka I.
    Muscle Nerve; 1984 Oct 11; 7(8):629-35. PubMed ID: 6543909
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  • 19. 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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  • 20. Hyperekplexia in a neonate: a novel finding in Fukuyama type congenital muscular dystrophy.
    Tunc T, Mungan IA, Okulu E, Tiras ST, Tekin M, Atasay B, Arsan S, Turmen T.
    Genet Couns; 2009 Apr 07; 20(3):275-9. PubMed ID: 19852435
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