These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. 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]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle. Trevisan CP; Martinello F; Ferruzza E; Fanin M; Chevallay M; Tomé FM Childs Nerv Syst; 1996 Oct; 12(10):604-10. PubMed ID: 8934020 [TBL] [Abstract][Full Text] [Related]
8. [Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia]. Ribeiro VT; Moreira NC; Teixeira J; Guimarães A; Cruz R; Lima L Acta Med Port; 2003; 16(3):189-92. PubMed ID: 12868400 [TBL] [Abstract][Full Text] [Related]
9. MR imaging findings in children with merosin-deficient congenital muscular dystrophy. Caro PA; Scavina M; Hoffman E; Pegoraro E; Marks HG AJNR Am J Neuroradiol; 1999 Feb; 20(2):324-6. PubMed ID: 10094364 [TBL] [Abstract][Full Text] [Related]
10. 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 [TBL] [Abstract][Full Text] [Related]
12. Merosin and congenital muscular dystrophy. Miyagoe-Suzuki Y; Nakagawa M; Takeda S Microsc Res Tech; 2000 Feb 1-15; 48(3-4):181-91. PubMed ID: 10679965 [TBL] [Abstract][Full Text] [Related]
13. Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients. Farina L; Morandi L; Milanesi I; Ciceri E; Mora M; Moroni I; Pantaleoni C; Savoiardo M Neuroradiology; 1998 Dec; 40(12):807-11. PubMed ID: 9877136 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings. Topaloğlu H; Talim B; Vignier N; Helbling-Leclerc AH; Yetük M; Afşin IE; Cağlar M; Kale G; Guicheney P Neuromuscul Disord; 1998 May; 8(3-4):169-74. PubMed ID: 9631397 [TBL] [Abstract][Full Text] [Related]