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Journal Abstract Search

290 related items for PubMed ID: 9436431

  • 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. [Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)].
    Toda T.
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1419-21. PubMed ID: 8752416
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  • 23. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
    Brockington M, Blake DJ, Prandini P, Brown SC, Torelli S, Benson MA, Ponting CP, Estournet B, Romero NB, Mercuri E, Voit T, Sewry CA, Guicheney P, Muntoni F.
    Am J Hum Genet; 2001 Dec; 69(6):1198-209. PubMed ID: 11592034
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  • 24. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.
    Pegoraro E, Mancias P, Swerdlow SH, Raikow RB, Garcia C, Marks H, Crawford T, Carver V, Di Cianno B, Hoffman EP.
    Ann Neurol; 1996 Nov; 40(5):782-91. PubMed ID: 8957020
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  • 25. The childhood muscular dystrophies: making order out of chaos.
    Tsao CY, Mendell JR.
    Semin Neurol; 1999 Nov; 19(1):9-23. PubMed ID: 10711985
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  • 26. Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.
    Lamer S, Carlier RY, Pinard JM, Mompoint D, Bagard C, Burdairon E, Estournet B, Barois A, Vallée C.
    Radiology; 1998 Mar; 206(3):811-6. PubMed ID: 9494506
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  • 31. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
    Triki C, Louhichi N, Méziou M, Choyakh F, Kéchaou MS, Jlidi R, Mhiri C, Fakhfakh F, Ayadi H.
    Neuromuscul Disord; 2003 Jan; 13(1):4-12. PubMed ID: 12467726
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  • 34. Merosin-negative non-Fukuyama-type congenital muscular dystrophy: a case report.
    Yamashita Y, Ohtaka E, Matsuishi T, Osari S, Kobayashi O, Nonaka I.
    Brain Dev; 1996 Jan; 18(2):131-4. PubMed ID: 8733905
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  • 36. 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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  • 37. [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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  • 40. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle.
    Philpot J, Sewry C, Pennock J, Dubowitz V.
    Neuromuscul Disord; 1995 Jul; 5(4):301-5. PubMed ID: 7580243
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