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Journal Abstract Search

553 related items for PubMed ID: 7477753

  • 1. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
    Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R.
    Neuropediatrics; 1995 Jun; 26(3):148-55. PubMed ID: 7477753
    [Abstract] [Full Text] [Related]

  • 2. Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.
    Sewry CA, D'Alessandro M, Wilson LA, Sorokin LM, Naom I, Bruno S, Ferlini A, Dubowitz V, Muntoni F.
    Neuropediatrics; 1997 Aug; 28(4):217-22. PubMed ID: 9309712
    [Abstract] [Full Text] [Related]

  • 3. Congenital muscular dystrophy with merosin deficiency.
    Tomé FM, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Apr; 317(4):351-7. PubMed ID: 8000914
    [Abstract] [Full Text] [Related]

  • 4. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
    Nonaka I.
    Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
    [Abstract] [Full Text] [Related]

  • 5. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1997 Dec; 28(2):141-9. PubMed ID: 10101782
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?
    Mercuri E, Sewry CA, Brown SC, Brockington M, Jungbluth H, DeVile C, Counsell S, Manzur A, Muntoni F.
    Neuropediatrics; 2000 Aug 07; 31(4):186-9. PubMed ID: 11071142
    [Abstract] [Full Text] [Related]

  • 8. Merosin-deficient congenital muscular dystrophy type 1A.
    Buteică E, Roşulescu E, Burada F, Stănoiu B, Zăvăleanu M.
    Rom J Morphol Embryol; 2008 Aug 07; 49(2):229-33. PubMed ID: 18516331
    [Abstract] [Full Text] [Related]

  • 9. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
    Vainzof M, Marie SK, Reed UC, Schwartzman JS, Pavanello RC, Passos-Bueno MR, Zatz M.
    Neuropediatrics; 1995 Dec 07; 26(6):293-7. PubMed ID: 8719743
    [Abstract] [Full Text] [Related]

  • 10. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y, Nakagawa M, Takeda S.
    Microsc Res Tech; 1995 Dec 07; 48(3-4):181-91. PubMed ID: 10679965
    [Abstract] [Full Text] [Related]

  • 11. [Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia].
    Ribeiro VT, Moreira NC, Teixeira J, Guimarães A, Cruz R, Lima L.
    Acta Med Port; 2003 Dec 07; 16(3):189-92. PubMed ID: 12868400
    [Abstract] [Full Text] [Related]

  • 12. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I, Bushby K, Anderson L, Muntoni F, Tolvanen-Mahjneh H, Bashir R, Pizzi A, Brockington M, Marconi G.
    Neuropediatrics; 1999 Feb 07; 30(1):22-8. PubMed ID: 10222457
    [Abstract] [Full Text] [Related]

  • 13. Merosin-deficient congenital muscular dystrophy in Korea.
    Chae JH, Lee JS, Hwang H, Kim KJ, Hwang YS, Park JD, Cheon JE, Kim IO, Choe GY, Park SH.
    Brain Dev; 2009 May 07; 31(5):341-6. PubMed ID: 18723302
    [Abstract] [Full Text] [Related]

  • 14. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
    Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F.
    Hum Mol Genet; 2003 Nov 01; 12(21):2853-61. PubMed ID: 12966029
    [Abstract] [Full Text] [Related]

  • 15. Laminin-alpha 2 chain (merosin M) is preserved in the Walker-Warburg syndrome.
    Kükner S, Gürer Y, Saatçi I, Akçören Z, Topaloğlu H.
    Neuropediatrics; 1996 Oct 01; 27(5):279-80. PubMed ID: 8971752
    [No Abstract] [Full Text] [Related]

  • 16. Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2.
    Helbling-Leclerc A, Topaloglu H, Tomé FM, Sewry C, Gyapay G, Naom I, Muntoni F, Dubowitz V, Barois A, Estournet B.
    C R Acad Sci III; 1995 Dec 01; 318(12):1245-52. PubMed ID: 8745640
    [Abstract] [Full Text] [Related]

  • 17. [Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].
    Fardeau M, Tomé FM, Helbling-Leclerc A, Evangelista T, Ottolini A, Chevallay M, Barois A, Estournet B, Harpey JP, Fauré S, Guicheney P, Hillaire D.
    Rev Neurol (Paris); 1996 Jan 01; 152(1):11-9. PubMed ID: 8729391
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