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22. Brain MRI features of merosin-negative congenital muscular dystrophy. Ibrahim Abdulla JK; Vattoth S; Al Tawari AA; Pandey T; Abubacker S Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069 [TBL] [Abstract][Full Text] [Related]
23. [Significance of merosin and sarcoglycan in manifestations of certain forms of muscular dystrophy]. Medić S; Rakocević-Stojanović V Srp Arh Celok Lek; 1998; 126(1-2):34-9. PubMed ID: 9525081 [TBL] [Abstract][Full Text] [Related]
24. Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle. Cohn RD; Mayer U; Saher G; Herrmann R; van der Flier A; Sonnenberg A; Sorokin L; Voit T J Neurol Sci; 1999 Mar; 163(2):140-52. PubMed ID: 10371075 [TBL] [Abstract][Full Text] [Related]
25. Multiplex Western blotting system for the analysis of muscular dystrophy proteins. Anderson LV; Davison K Am J Pathol; 1999 Apr; 154(4):1017-22. PubMed ID: 10233840 [TBL] [Abstract][Full Text] [Related]
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29. Fukuyama-type congenital muscular dystrophy: close relation between changes in the muscle basal lamina and plasma membrane. Matsubara S; Mizuno Y; Kitaguchi T; Isozaki E; Miyamoto K; Hirai S Neuromuscul Disord; 1999 Oct; 9(6-7):388-98. PubMed ID: 10545042 [TBL] [Abstract][Full Text] [Related]
30. Expression of laminin subunits in congenital muscular dystrophy. Sewry CA; Philpot J; Mahony D; Wilson LA; Muntoni F; Dubowitz V Neuromuscul Disord; 1995 Jul; 5(4):307-16. PubMed ID: 7580244 [TBL] [Abstract][Full Text] [Related]
31. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status. Mercuri E; Muntoni F; Berardinelli A; Pennock J; Sewry C; Philpot J; Dubowitz V Neuropediatrics; 1995 Feb; 26(1):3-7. PubMed ID: 7791947 [TBL] [Abstract][Full Text] [Related]
32. Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency. Reed UC; Marie SK; Vainzof M; Salum PB; Levy JA; Zatz M; Diament A Brain Dev; 1996; 18(1):53-8. PubMed ID: 8907344 [TBL] [Abstract][Full Text] [Related]
33. Normal expression of adhalin and merosin in ovine congenital progressive muscular dystrophy. Johnsen RD; Laing NG; Huxtable CR; Kakulas BA Aust Vet J; 1997 Mar; 75(3):215-6. PubMed ID: 9088516 [No Abstract] [Full Text] [Related]
34. Merosin negative congenital muscular dystrophy: a short report. Ralte AM; Sharma MC; Gulati S; Das M; Sarkar C Neurol India; 2003 Sep; 51(3):417-9. PubMed ID: 14652462 [TBL] [Abstract][Full Text] [Related]
35. Sequential neuroradiological and neurophysiological studies in a Japanese girl with merosin-deficient congenital muscular dystrophy. Fujii Y; Sugiura C; Fukuda C; Maegaki Y; Ohno K Brain Dev; 2011 Feb; 33(2):140-4. PubMed ID: 20303224 [TBL] [Abstract][Full Text] [Related]
37. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study. Flanigan KM; Kerr L; Bromberg MB; Leonard C; Tsuruda J; Zhang P; Gonzalez-Gomez I; Cohn R; Campbell KP; Leppert M Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485 [TBL] [Abstract][Full Text] [Related]
38. [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]
39. Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation. Voit T; Cohn RD; Sperner J; Leube B; Sorokin L; Toda T; Herrmann R Neuromuscul Disord; 1999 Mar; 9(2):95-101. PubMed ID: 10220864 [TBL] [Abstract][Full Text] [Related]
40. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle. Philpot J; Sewry C; Pennock J; Dubowitz V Neuromuscul Disord; 1995 Jul; 5(4):301-5. PubMed ID: 7580243 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]