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.
134 related articles for article (PubMed ID: 7580244)
41. Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse. Matsumura K; Yamada H; Saito F; Sunada Y; Shimizu T Neuromuscul Disord; 1997 Jan; 7(1):7-12. PubMed ID: 9132144 [TBL] [Abstract][Full Text] [Related]
42. Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome. Vajsar J; Ackerley C; Chitayat D; Becker LE Pediatr Neurol; 2000 Feb; 22(2):139-43. PubMed ID: 10738921 [TBL] [Abstract][Full Text] [Related]
43. 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]
44. Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. Herrmann R; Straub V; Meyer K; Kahn T; Wagner M; Voit T Eur J Pediatr; 1996 Nov; 155(11):968-76. PubMed ID: 8911899 [TBL] [Abstract][Full Text] [Related]
45. Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers. Vainzof M; Richard P; Herrmann R; Jimenez-Mallebrera C; Talim B; Yamamoto LU; Ledeuil C; Mein R; Abbs S; Brockington M; Romero NB; Zatz M; Topaloglu H; Voit T; Sewry C; Muntoni F; Guicheney P; Tomé FM Neuromuscul Disord; 2005 Oct; 15(9-10):588-94. PubMed ID: 16084089 [TBL] [Abstract][Full Text] [Related]
46. Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency. Minetti C; Bado M; Morreale G; Pedemonte M; Cordone G Neurology; 1996 May; 46(5):1354-8. PubMed ID: 8628482 [TBL] [Abstract][Full Text] [Related]
54. [Immunohistochemical studies of a variant of congenital muscular dystrophy]. Yoshioka M; Sugie K; Nishino I; Toda T No To Hattatsu; 2004 Jan; 36(1):55-9. PubMed ID: 14737865 [TBL] [Abstract][Full Text] [Related]
55. Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain. Allamand V; Sunada Y; Salih MA; Straub V; Ozo CO; Al-Turaiki MH; Akbar M; Kolo T; Colognato H; Zhang X; Sorokin LM; Yurchenco PD; Tryggvason K; Campbell KP Hum Mol Genet; 1997 May; 6(5):747-52. PubMed ID: 9158149 [TBL] [Abstract][Full Text] [Related]
56. Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigation. Yamamoto T; Shibata N; Kanazawa M; Kobayashi M; Komori T; Ikeya K; Kondo E; Saito K; Osawa M Acta Neuropathol; 1997 Aug; 94(2):173-9. PubMed ID: 9255393 [TBL] [Abstract][Full Text] [Related]
57. 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]
58. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. Higuchi I; Yamada H; Fukunaga H; Iwaki H; Okubo R; Nakagawa M; Osame M; Roberds SL; Shimizu T; Campbell KP J Clin Invest; 1994 Aug; 94(2):601-6. PubMed ID: 8040315 [TBL] [Abstract][Full Text] [Related]
59. 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]
60. 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] [Previous] [Next] [New Search]