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Journal Abstract Search

169 related items for PubMed ID: 9448020

  • 1. 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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  • 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
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  • 4. [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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  • 5. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1996 Jan; 28(2):141-9. PubMed ID: 10101782
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  • 13. 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 Jan; 61(5):481-7. PubMed ID: 24262449
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  • 15. MR imaging of pelvic and thigh muscles in congenital muscular dystrophy.
    Oto A, Aydingöz U, Başgün N, Talim B, Karaağaoğlu E, Topaloğlu H.
    Turk J Pediatr; 2001 Jan; 43(1):44-51. PubMed ID: 11297158
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  • 16. Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy.
    Talim B, Kale G, Topaloglu H, Akçören Z, Caglar M, Gögüş S, Elkay M.
    Pediatr Dev Pathol; 2000 Jan; 3(2):168-76. PubMed ID: 10679036
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