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Journal Abstract Search

377 related items for PubMed ID: 9309712

  • 21. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
    [Abstract] [Full Text] [Related]

  • 22. 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 07; 122(1):69-71. PubMed ID: 9448020
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  • 23. 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 07; 54(3):193-8. PubMed ID: 9788720
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  • 24. Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.
    Louhichi N, Richard P, Triki CH, Meziou M, Ayadi H, Guicheney P, Fakhfakh F.
    Arch Inst Pasteur Tunis; 2006 Sep 07; 83(1-4):19-23. PubMed ID: 19388593
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  • 25. Merosin negative congenital muscular dystrophy: a short report.
    Ralte AM, Sharma MC, Gulati S, Das M, Sarkar C.
    Neurol India; 2003 Sep 07; 51(3):417-9. PubMed ID: 14652462
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  • 26. [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 Sep 07; 217(5):281-5. PubMed ID: 16167276
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  • 27. Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice.
    Ringelmann B, Röder C, Hallmann R, Maley M, Davies M, Grounds M, Sorokin L.
    Exp Cell Res; 1999 Jan 10; 246(1):165-82. PubMed ID: 9882526
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  • 29. 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 10; 3(2):168-76. PubMed ID: 10679036
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  • 30. Congenital muscular dystrophy with merosin deficiency.
    Tomé FM, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Apr 10; 317(4):351-7. PubMed ID: 8000914
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  • 32. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy.
    Shorer Z, Philpot J, Muntoni F, Sewry C, Dubowitz V.
    J Child Neurol; 1995 Nov 10; 10(6):472-5. PubMed ID: 8576559
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  • 34. 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 Nov 10; 61(5):481-7. PubMed ID: 24262449
    [Abstract] [Full Text] [Related]

  • 35. Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophy.
    Vainzof M, Costa CS, Marie SK, Moreira ES, Reed U, Passos-Bueno MR, Beggs AH, Zatz M.
    Neuropediatrics; 1997 Aug 10; 28(4):223-8. PubMed ID: 9309713
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  • 37. Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.
    Nissinen M, Helbling-Leclerc A, Zhang X, Evangelista T, Topaloglu H, Cruaud C, Weissenbach J, Fardeau M, Tomé FM, Schwartz K, Tryggvason K, Guicheney P.
    Am J Hum Genet; 1996 Jun 10; 58(6):1177-84. PubMed ID: 8651294
    [Abstract] [Full Text] [Related]

  • 38. [A unique case of congenital muscular dystrophy].
    Hermanová M, Vondrácek P, Lukás Z.
    Cesk Patol; 2004 Apr 10; 40(2):57-62. PubMed ID: 15233018
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  • 39. Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.
    Mercuri E, Dubowitz L, Berardinelli A, Pennock J, Jongmans M, Henderson S, Muntoni F, Sewry C, Philpot J, Dubowitz V.
    Neuropediatrics; 1995 Jun 10; 26(3):156-62. PubMed ID: 7477754
    [Abstract] [Full Text] [Related]

  • 40. [Congenital muscular dystrophy and merosin deficiency].
    Werneck LC, Scola RH, Iwamoto FM.
    Arq Neuropsiquiatr; 1997 Dec 10; 55(4):780-7. PubMed ID: 9629338
    [Abstract] [Full Text] [Related]

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