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Journal Abstract Search

229 related items for PubMed ID: 24262449

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Brain MRI features of merosin-negative congenital muscular dystrophy.
    Ibrahim Abdulla JK, Vattoth S, Al Tawari AA, Pandey T, Abubacker S.
    Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069
    [Abstract] [Full Text] [Related]

  • 3. Merosin-deficient congenital muscular dystrophy in Korea.
    Chae JH, Lee JS, Hwang H, Kim KJ, Hwang YS, Park JD, Cheon JE, Kim IO, Choe GY, Park SH.
    Brain Dev; 2009 May; 31(5):341-6. PubMed ID: 18723302
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1997 Aug; 28(2):141-9. PubMed ID: 10101782
    [Abstract] [Full Text] [Related]

  • 6. [Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].
    Xiong H, Yao S, Yuan Y, Chang XZ, Wu Y, Bao XH, Zhang YH, Wu HS, Chen L, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2006 Dec; 44(12):918-23. PubMed ID: 17254461
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.
    Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F.
    Eur J Paediatr Neurol; 2000 Jan; 4(3):109-14. PubMed ID: 10872105
    [Abstract] [Full Text] [Related]

  • 12. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
    Nonaka I.
    Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

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

  • 15. Congenital myopathies and muscular dystrophies.
    Gilbreath HR, Castro D, Iannaccone ST.
    Neurol Clin; 2014 Aug; 32(3):689-703, viii. PubMed ID: 25037085
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
    Vainzof M, Marie SK, Reed UC, Schwartzman JS, Pavanello RC, Passos-Bueno MR, Zatz M.
    Neuropediatrics; 1995 Dec; 26(6):293-7. PubMed ID: 8719743
    [Abstract] [Full Text] [Related]

  • 18. Telethonin-deficiency initially presenting as a congenital muscular dystrophy.
    Ferreiro A, Mezmezian M, Olivé M, Herlicoviez D, Fardeau M, Richard P, Romero NB.
    Neuromuscul Disord; 2011 Jun; 21(6):433-8. PubMed ID: 21530252
    [Abstract] [Full Text] [Related]

  • 19. Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation.
    Reed UC, Tsanaclis AM, Vainzof M, Marie SK, Carvalho MS, Roizenblatt J, Pedreira CC, Diament A, Levy JA.
    Brain Dev; 1999 Jun; 21(4):274-8. PubMed ID: 10392752
    [Abstract] [Full Text] [Related]

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