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Journal Abstract Search

153 related items for PubMed ID: 8719743

  • 1. 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; 26(6):293-7. PubMed ID: 8719743
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  • 2. 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
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  • 3. [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
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  • 4. 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
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  • 5. Brain MRI features of merosin-negative congenital muscular dystrophy.
    Ibrahim Abdulla JK, Vattoth S, Al Tawari AA, Pandey T, Abubacker S.
    Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069
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  • 6. Merosin-deficient congenital muscular dystrophy type 1A.
    Buteică E, Roşulescu E, Burada F, Stănoiu B, Zăvăleanu M.
    Rom J Morphol Embryol; 2008 Dec; 49(2):229-33. PubMed ID: 18516331
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  • 7. 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 Dec; 4(3):109-14. PubMed ID: 10872105
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  • 8. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 2000 Dec; 28(2):141-9. PubMed ID: 10101782
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  • 10. [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; 16(3):189-92. PubMed ID: 12868400
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  • 14. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.
    van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J.
    Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685
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  • 18. 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; 31(5):341-6. PubMed ID: 18723302
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  • 20. Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.
    Lamer S, Carlier RY, Pinard JM, Mompoint D, Bagard C, Burdairon E, Estournet B, Barois A, Vallée C.
    Radiology; 1998 Mar; 206(3):811-6. PubMed ID: 9494506
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