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7. 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]
8. [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 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Matsumura K; Yamada H; Saito F; Sunada Y; Shimizu T Neuromuscul Disord; 1997 Jan; 7(1):7-12. PubMed ID: 9132144 [TBL] [Abstract][Full Text] [Related]
12. Merosin positive congenital muscular dystrophy with severe involvement of the central nervous system. De Stefano N; Dotti MT; Villanova M; Scarano G; Federico A Brain Dev; 1996; 18(4):323-6. PubMed ID: 8879654 [TBL] [Abstract][Full Text] [Related]
13. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations. Vainzof M; Marie SK; Reed UC; Schwartzman JS; Pavanello RC; Passos-Bueno MR; Zatz M Neuropediatrics; 1995 Dec; 26(6):293-7. PubMed ID: 8719743 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. 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]
16. 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]
17. 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]
18. 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]