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Journal Abstract Search

553 related items for PubMed ID: 7477753

  • 21. 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
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  • 22. Beyond dystrophin: current progress in the muscular dystrophies.
    Bönnemann CG, McNally EM, Kunkel LM.
    Curr Opin Pediatr; 1996 Dec; 8(6):569-82. PubMed ID: 9018440
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  • 23. 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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  • 24. Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
    Helbling-Leclerc A, Zhang X, Topaloglu H, Cruaud C, Tesson F, Weissenbach J, Tomé FM, Schwartz K, Fardeau M, Tryggvason K.
    Nat Genet; 1995 Oct; 11(2):216-8. PubMed ID: 7550355
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  • 30. The childhood muscular dystrophies: making order out of chaos.
    Tsao CY, Mendell JR.
    Semin Neurol; 1999 Oct; 19(1):9-23. PubMed ID: 10711985
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  • 31. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
    Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, Muntoni F.
    Neuromuscul Disord; 1999 Mar; 9(2):81-5. PubMed ID: 10220862
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  • 32. 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
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  • 34. 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
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  • 37. Congenital muscular dystrophies.
    Kirschner J.
    Handb Clin Neurol; 2013 Nov; 113():1377-85. PubMed ID: 23622361
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  • 38. [Type II lissencephaly: presentation of intermediate form].
    Palomero-Domínguez MA, Ramos-Fernández JM, Domínguez-Santurino F, Ruiz-Gómez M.
    Rev Neurol; 1998 Oct; 27(158):594-6. PubMed ID: 9803503
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  • 39. 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(6):472-5. PubMed ID: 8576559
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  • 40. [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
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