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Journal Abstract Search

320 related items for PubMed ID: 10872105

  • 1. 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; 4(3):109-14. PubMed ID: 10872105
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  • 3. 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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  • 4. Merosin-negative congenital muscular dystrophy: magnetic resonance spectroscopy findings.
    Aslan M, Alkan A, Yakinci C, Sonmezgoz E, Bicak U, Zorludemir S.
    Brain Dev; 2005 Jun; 27(4):308-10. PubMed ID: 15862197
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  • 5. 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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  • 7. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y, Nakagawa M, Takeda S.
    Microsc Res Tech; 1997 Aug; 48(3-4):181-91. PubMed ID: 10679965
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  • 9. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1997 Aug; 28(2):141-9. PubMed ID: 10101782
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  • 10. 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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  • 13. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
    Nonaka I.
    Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
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  • 14. 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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  • 15. Occipito-temporal polymicrogyria and subclinical muscular dystrophy.
    Zolkipli Z, Hartley L, Brown S, Rutherford M, Cowan F, Mercuri E, Muntoni F.
    Neuropediatrics; 2003 Apr; 34(2):92-5. PubMed ID: 12776231
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  • 16. 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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  • 20. Changes in cerebral white matter in a case of congenital muscular dystrophy (non-Fukuyama type).
    Tanaka J, Mimaki T, Okada S, Fujimura H.
    Neuropediatrics; 1990 Nov; 21(4):183-6. PubMed ID: 2290477
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