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5. Congenital muscular dystrophy with merosin deficiency. Tomé FM; Evangelista T; Leclerc A; Sunada Y; Manole E; Estournet B; Barois A; Campbell KP; Fardeau M C R Acad Sci III; 1994 Apr; 317(4):351-7. PubMed ID: 8000914 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. Merosin-deficient congenital muscular dystrophy type 1A. Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331 [TBL] [Abstract][Full Text] [Related]
8. [Non-Fukuyama type merosin-positive congenital muscular dystrophy with delayed muscle fiber type differentiation: a case report]. Korematsu S; Kobayashi O; Fukushima N; Sawaguchi H; Ishihara T; Izumi T; Ogawa T; Nonaka I No To Hattatsu; 1995 Jul; 27(4):309-14. PubMed ID: 7612293 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblings. Ruggieri V; Lubieniecki F; Meli F; Diaz D; Ferragut E; Saito K; Brockington M; Muntoni F; Fukuyama Y; Taratuto AL Neuromuscul Disord; 2001 Sep; 11(6-7):570-8. PubMed ID: 11525887 [TBL] [Abstract][Full Text] [Related]
12. Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter. Echenne B; Rivier F; Jellali AJ; Azais M; Mornet D; Pons F Neuromuscul Disord; 1997 May; 7(3):187-90. PubMed ID: 9185183 [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 secondary merosin deficiency and normal brain MRI: a novel entity? Mercuri E; Sewry CA; Brown SC; Brockington M; Jungbluth H; DeVile C; Counsell S; Manzur A; Muntoni F Neuropediatrics; 2000 Aug; 31(4):186-9. PubMed ID: 11071142 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy. Spyrou N; Philpot J; Foale R; Camici PG; Muntoni F Am Heart J; 1998 Sep; 136(3):474-6. PubMed ID: 9736139 [TBL] [Abstract][Full Text] [Related]