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Journal Abstract Search

139 related items for PubMed ID: 9327401

  • 1.
    ; . PubMed ID:
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  • 2. Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study.
    ter Laak HJ, Leyten QH, Gabreëls FJ, Kuppen H, Renier WO, Sengers RC.
    Clin Neurol Neurosurg; 1998 Mar; 100(1):5-10. PubMed ID: 9637197
    [Abstract] [Full Text] [Related]

  • 3. Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy.
    Marbini A, Bellanova MF, Ferrari A, Lodesani M, Gemignani F.
    Acta Neuropathol; 1997 Aug; 94(2):103-8. PubMed ID: 9255383
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  • 4. 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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  • 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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  • 6. Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry.
    Herrmann R, Straub V, Meyer K, Kahn T, Wagner M, Voit T.
    Eur J Pediatr; 1996 Nov; 155(11):968-76. PubMed ID: 8911899
    [Abstract] [Full Text] [Related]

  • 7. 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 Nov; 3(2):168-76. PubMed ID: 10679036
    [Abstract] [Full Text] [Related]

  • 8. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy.
    Li M, Dickson DW, Spiro AJ.
    Arch Neurol; 1997 Dec; 54(12):1457-61. PubMed ID: 9400354
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  • 10. Severe classical congenital muscular dystrophy and merosin expression.
    Vajsar J, Chitayat D, Becker LE, Ho M, Ben-Zeev B, Jay V.
    Clin Genet; 1998 Sep; 54(3):193-8. PubMed ID: 9788720
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  • 12. [Congenital muscular dystrophy and merosin deficiency].
    Werneck LC, Scola RH, Iwamoto FM.
    Arq Neuropsiquiatr; 1997 Dec; 55(4):780-7. PubMed ID: 9629338
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  • 15. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1997 Dec; 28(2):141-9. PubMed ID: 10101782
    [Abstract] [Full Text] [Related]

  • 16. [A unique case of congenital muscular dystrophy].
    Hermanová M, Vondrácek P, Lukás Z.
    Cesk Patol; 2004 Apr; 40(2):57-62. PubMed ID: 15233018
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  • 17. 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 Apr; 61(5):481-7. PubMed ID: 24262449
    [Abstract] [Full Text] [Related]

  • 18. Abnormal localization of laminin subunits in muscular dystrophies.
    Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K.
    J Neurol Sci; 1993 Oct; 119(1):53-64. PubMed ID: 8246011
    [Abstract] [Full Text] [Related]

  • 19. Expression of laminin subunits in congenital muscular dystrophy.
    Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni F, Dubowitz V.
    Neuromuscul Disord; 1995 Jul; 5(4):307-16. PubMed ID: 7580244
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