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22. Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI. Leite CC; Lucato LT; Martin MG; Ferreira LG; Resende MB; Carvalho MS; Marie SK; Jinkins JR; Reed UC Pediatr Radiol; 2005 Jun; 35(6):572-9. PubMed ID: 15750812 [TBL] [Abstract][Full Text] [Related]
23. Merosin-deficient congenital muscular dystrophy type 1A. Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331 [TBL] [Abstract][Full Text] [Related]
24. [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 [TBL] [Abstract][Full Text] [Related]
25. 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; 3(2):168-76. PubMed ID: 10679036 [TBL] [Abstract][Full Text] [Related]
26. 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 [TBL] [Abstract][Full Text] [Related]
27. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status. Mercuri E; Muntoni F; Berardinelli A; Pennock J; Sewry C; Philpot J; Dubowitz V Neuropediatrics; 1995 Feb; 26(1):3-7. PubMed ID: 7791947 [TBL] [Abstract][Full Text] [Related]
28. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms]. Nonaka I Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431 [TBL] [Abstract][Full Text] [Related]
29. 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 [TBL] [Abstract][Full Text] [Related]
30. Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases. Ferreira LG; Marie SK; Liu EC; Resende MB; Carvalho MS; Scaff M; Reed UC Arq Neuropsiquiatr; 2005 Sep; 63(3B):791-800. PubMed ID: 16258658 [TBL] [Abstract][Full Text] [Related]
31. 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 [TBL] [Abstract][Full Text] [Related]
33. Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin. Tachi N; Ohya K; Chiba S; Matsuo M; Patria SY; Matsumura K Neurology; 1997 Aug; 49(2):579-83. PubMed ID: 9270600 [TBL] [Abstract][Full Text] [Related]
34. Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy. Mercuri E; Pennock J; Goodwin F; Sewry C; Cowan F; Dubowitz L; Dubowitz V; Muntoni F Neuromuscul Disord; 1996 Dec; 6(6):425-9. PubMed ID: 9027850 [TBL] [Abstract][Full Text] [Related]
38. Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up. Trevisan CP; Martinello F; Ferruzza E; Angelini C Eur Neurol; 1995; 35(4):230-5. PubMed ID: 7671985 [TBL] [Abstract][Full Text] [Related]
39. 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 [TBL] [Abstract][Full Text] [Related]
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