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.
185 related articles for article (PubMed ID: 10392752)
1. Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation. Reed UC; Tsanaclis AM; Vainzof M; Marie SK; Carvalho MS; Roizenblatt J; Pedreira CC; Diament A; Levy JA Brain Dev; 1999 Jun; 21(4):274-8. PubMed ID: 10392752 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings. Topaloğlu H; Talim B; Vignier N; Helbling-Leclerc AH; Yetük M; Afşin IE; Cağlar M; Kale G; Guicheney P Neuromuscul Disord; 1998 May; 8(3-4):169-74. PubMed ID: 9631397 [TBL] [Abstract][Full Text] [Related]
7. Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: a new entity in two families. Topaloğlu H; Yetük M; Talim B; Akçören Z; Cağlar M Eur J Paediatr Neurol; 1997; 1(4):127-31. PubMed ID: 10728208 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
11. 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]
12. Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. Reed UC; Marie SK; Vainzof M; Gobbo LF; Gurgel JE; Carvalho MS; Resende MB; Espíndola AA; Zatz M; Diament A J Child Neurol; 2000 Mar; 15(3):172-8. PubMed ID: 10757473 [TBL] [Abstract][Full Text] [Related]
13. 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]
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]