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PUBMED FOR HANDHELDS

Journal Abstract Search

280 related items for PubMed ID: 8729391

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  • 5. 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
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  • 6. 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
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  • 7. [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 Dec; 217(5):281-5. PubMed ID: 16167276
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  • 14. [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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  • 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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  • 18. Immunohistochemical evaluation of merosin deficiency in congenital muscular dystrophies.
    Brett FM, Loring P, Caesar A, Burke M, Brennan RP, King M, Farrell MA.
    Arch Pathol Lab Med; 1998 Jan; 122(1):69-71. PubMed ID: 9448020
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  • 20. 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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