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24. 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]
25. Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study. Taratuto AL; Lubieniecki F; Díaz D; Schultz M; Ruggieri V; Saccoliti M; Dubrovsky A Neuromuscul Disord; 1999 Mar; 9(2):86-94. PubMed ID: 10220863 [TBL] [Abstract][Full Text] [Related]
26. Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy. Martinello F; Angelini C; Trevisan CP Eur Neurol; 1998 Jul; 40(1):37-45. PubMed ID: 9693231 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. A case of merosin-negative congenital muscular dystrophy with extensive white matter abnormalities and electroencephalographic changes in a Syrian boy. Al-Ajmi MO; Abdulla JK; Neubauer D J Med Liban; 2001; 49(3):173-8. PubMed ID: 12184464 [TBL] [Abstract][Full Text] [Related]
30. [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]
31. 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]
36. Merosin-deficient congenital muscular dystrophy in two siblings. Hui CM; Kwong L; Lam SY; Loo KT Hong Kong Med J; 2004 Dec; 10(6):423-6. PubMed ID: 15591603 [TBL] [Abstract][Full Text] [Related]
37. [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]
38. High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy. Dubowitz DJ; Tyszka JM; Sewry CA; Moats RA; Scadeng M; Dubowitz V Neuromuscul Disord; 2000 Jun; 10(4-5):292-8. PubMed ID: 10838257 [TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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] [Previous] [Next] [New Search]