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. Congenital muscular dystrophy. Huang FL; Mak SC; Chi CS Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931 [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. Merosin-positive congenital muscular dystrophy: a large inbred family. Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy. Mercuri E; Anker S; Philpot J; Sewry C; Dubowitz V; Muntoni F Pediatr Neurol; 1998 May; 18(5):399-401. PubMed ID: 9650678 [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. 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]
12. The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review. Jones KJ; Morgan G; Johnston H; Tobias V; Ouvrier RA; Wilkinson I; North KN J Med Genet; 2001 Oct; 38(10):649-57. PubMed ID: 11584042 [TBL] [Abstract][Full Text] [Related]
13. Congenital muscular dystrophy. A histochemical study with morphometric analysis on biopsied muscles. Kihira S; Nonaka I J Neurol Sci; 1985 Sep; 70(2):139-49. PubMed ID: 4056819 [TBL] [Abstract][Full Text] [Related]
14. Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy. Marbini A; Bellanova MF; Ferrari A; Lodesani M; Gemignani F Acta Neuropathol; 1997 Aug; 94(2):103-8. PubMed ID: 9255383 [TBL] [Abstract][Full Text] [Related]
15. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder]. Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Alonso-Martín A; Morales-Redondo R; Eirís-Puñal J Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819 [TBL] [Abstract][Full Text] [Related]
16. 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]