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.
137 related articles for article (PubMed ID: 9185183)
1. 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]
2. Abnormalities of dystrophin, the sarcoglycans, and laminin alpha2 in the muscular dystrophies. Jones KJ; Kim SS; North KN J Med Genet; 1998 May; 35(5):379-86. PubMed ID: 9610800 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
6. Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families. Pini A; Merlini L; Tomé FM; Chevallay M; Gobbi G Brain Dev; 1996; 18(4):316-22. PubMed ID: 8879653 [TBL] [Abstract][Full Text] [Related]
7. Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities. Mora M; Moroni I; Uziel G; di Blasi C; Barresi R; Farina L; Morandi L Neuromuscul Disord; 1996 Oct; 6(5):377-81. PubMed ID: 8938702 [TBL] [Abstract][Full Text] [Related]
8. Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy. Ishii H; Hayashi YK; Nonaka I; Arahata K Neuromuscul Disord; 1997 May; 7(3):191-7. PubMed ID: 9185184 [TBL] [Abstract][Full Text] [Related]
9. 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-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. 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]
13. The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin. Hayashi YK; Mizuno Y; Yoshida M; Nonaka I; Ozawa E; Arahata K Neurology; 1995 Mar; 45(3 Pt 1):551-4. PubMed ID: 7898714 [TBL] [Abstract][Full Text] [Related]
15. Immunogold localization of adhalin, alpha-dystroglycan and laminin in normal and dystrophic skeletal muscle. Cullen MJ; Walsh J; Roberds SL; Campbell KP Biochem Soc Trans; 1996 May; 24(2):274S. PubMed ID: 8736932 [No Abstract] [Full Text] [Related]
16. Congenital muscular dystrophy in Israeli families. Rachmiel M; Nevo Y; Lahat E; Kutai M; Harel S; Shahar E J Child Neurol; 2002 May; 17(5):333-6. PubMed ID: 12150578 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy. Kumar S; Aroor S; Mundkur S; Kumar M BMJ Case Rep; 2014 Mar; 2014():. PubMed ID: 24604798 [TBL] [Abstract][Full Text] [Related]
19. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects. Handa V; Mital A; Gupta M; Goyle S Neurol India; 2001 Mar; 49(1):19-24. PubMed ID: 11303236 [TBL] [Abstract][Full Text] [Related]
20. Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci. Talim B; Ferreiro A; Cormand B; Vignier N; Oto A; Göğüş S; Cila A; Lehesjoki AE; Pihko H; Guicheney P; Topaloğlu H Neuromuscul Disord; 2000 Dec; 10(8):548-52. PubMed ID: 11053680 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]