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. 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]
6. 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]
7. 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]
8. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy. Li M; Dickson DW; Spiro AJ Arch Neurol; 1997 Dec; 54(12):1457-61. PubMed ID: 9400354 [TBL] [Abstract][Full Text] [Related]
9. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining. Connolly AM; Pestronk A; Planer GJ; Yue J; Mehta S; Choksi R Neurology; 1996 Mar; 46(3):810-14. PubMed ID: 8618688 [TBL] [Abstract][Full Text] [Related]
10. Severe classical congenital muscular dystrophy and merosin expression. Vajsar J; Chitayat D; Becker LE; Ho M; Ben-Zeev B; Jay V Clin Genet; 1998 Sep; 54(3):193-8. PubMed ID: 9788720 [TBL] [Abstract][Full Text] [Related]
11. Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain. Sewry CA; Naom I; D'Alessandro M; Sorokin L; Bruno S; Wilson LA; Dubowitz V; Muntoni F Neuromuscul Disord; 1997 May; 7(3):169-75. PubMed ID: 9185180 [TBL] [Abstract][Full Text] [Related]
12. [Congenital muscular dystrophy and merosin deficiency]. Werneck LC; Scola RH; Iwamoto FM Arq Neuropsiquiatr; 1997 Dec; 55(4):780-7. PubMed ID: 9629338 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Alterations of the retino-cortical conduction in patients affected by classical congenital muscular dystrophy (CI-CMD) with merosin deficiency. Tormene AP; Trevisan C; Martinello F; Riva C; Pastorello E Doc Ophthalmol; 1999; 98(2):127-38. PubMed ID: 10946999 [TBL] [Abstract][Full Text] [Related]
15. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency]. Smeyers P Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782 [TBL] [Abstract][Full Text] [Related]
16. [A unique case of congenital muscular dystrophy]. Hermanová M; Vondrácek P; Lukás Z Cesk Patol; 2004 Apr; 40(2):57-62. PubMed ID: 15233018 [TBL] [Abstract][Full Text] [Related]
17. 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 [TBL] [Abstract][Full Text] [Related]
18. Abnormal localization of laminin subunits in muscular dystrophies. Hayashi YK; Engvall E; Arikawa-Hirasawa E; Goto K; Koga R; Nonaka I; Sugita H; Arahata K J Neurol Sci; 1993 Oct; 119(1):53-64. PubMed ID: 8246011 [TBL] [Abstract][Full Text] [Related]
19. Expression of laminin subunits in congenital muscular dystrophy. Sewry CA; Philpot J; Mahony D; Wilson LA; Muntoni F; Dubowitz V Neuromuscul Disord; 1995 Jul; 5(4):307-16. PubMed ID: 7580244 [TBL] [Abstract][Full Text] [Related]
20. Localization of laminin chains in the human retina: possible implications for congenital muscular dystrophy associated with alpha 2-chain of laminin deficiency. Toti P; De Felice C; Malandrini A; Megha T; Cardone C; Villanova M Neuromuscul Disord; 1997 Jan; 7(1):21-5. PubMed ID: 9132136 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]