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Journal Abstract Search

281 related items for PubMed ID: 17254461

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  • 4. A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade.
    Nagappa M, Atchayaram N, Narayanappa G.
    Neurol India; 2013; 61(5):481-7. PubMed ID: 24262449
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  • 6. [Congenital muscular dystrophy with laminin-a2 deficiency in early infancy: diagnosis and long-term follow-up].
    Panteliadis C, Karatza E, Xinias I, Flaris N, Tzitiridou M, Ramantani G.
    Klin Padiatr; 2005; 217(5):281-5. PubMed ID: 16167276
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  • 9. 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
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  • 12. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
    Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, Voit T, Sewry CA, Guicheney P, Muntoni F.
    Am J Hum Genet; 2001 Dec; 69(6):1198-209. PubMed ID: 11592034
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  • 14. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse.
    Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T.
    Neuromuscul Disord; 1997 Jan; 7(1):7-12. PubMed ID: 9132144
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  • 15. 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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  • 16. [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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  • 17. 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
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