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Journal Abstract Search

290 related items for PubMed ID: 9436431

  • 1. [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]

  • 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. 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]

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

  • 5. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y, Nakagawa M, Takeda S.
    Microsc Res Tech; 2008 Jun; 48(3-4):181-91. PubMed ID: 10679965
    [Abstract] [Full Text] [Related]

  • 6. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 2008 Jun; 28(2):141-9. PubMed ID: 10101782
    [Abstract] [Full Text] [Related]

  • 7. [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 Jun; 16(3):189-92. PubMed ID: 12868400
    [Abstract] [Full Text] [Related]

  • 8. [Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
    Toda T, Kobayashi K.
    Nihon Rinsho; 1997 Dec; 55(12):3169-75. PubMed ID: 9436430
    [Abstract] [Full Text] [Related]

  • 9. 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; 31(4):186-9. PubMed ID: 11071142
    [Abstract] [Full Text] [Related]

  • 10. Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin alpha-2 gene.
    Coral-Vazquez RM, Rosas-Vargas H, Meza-Espinosa P, Mendoza I, Huicochea JC, Ramon G, Salamanca F.
    J Hum Genet; 2003 Aug; 48(2):91-5. PubMed ID: 12601554
    [Abstract] [Full Text] [Related]

  • 11. [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; 152(1):11-9. PubMed ID: 8729391
    [Abstract] [Full Text] [Related]

  • 12. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping.
    Hillaire D, Leclerc A, Fauré S, Topaloglu H, Chiannilkulchaï N, Guicheney P, Grinas L, Legos P, Philpot J, Evangelista T.
    Hum Mol Genet; 1994 Sep; 3(9):1657-61. PubMed ID: 7833925
    [Abstract] [Full Text] [Related]

  • 13. 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; 30(1):22-8. PubMed ID: 10222457
    [Abstract] [Full Text] [Related]

  • 14. 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; 318(12):1245-52. PubMed ID: 8745640
    [Abstract] [Full Text] [Related]

  • 15. Merosin negative congenital muscular dystrophy: a short report.
    Ralte AM, Sharma MC, Gulati S, Das M, Sarkar C.
    Neurol India; 2003 Sep; 51(3):417-9. PubMed ID: 14652462
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.
    Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F.
    Eur J Paediatr Neurol; 2000 Apr; 4(3):109-14. PubMed ID: 10872105
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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]

  • 20. Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
    Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tomé FM, Schwartz K, Fardeau M, Tryggvason K.
    Nat Genet; 1995 Oct 07; 11(2):216-8. PubMed ID: 7550355
    [Abstract] [Full Text] [Related]

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