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27. Identification of Duchenne muscular dystrophy carriers. Electron microscopical investigation of skeletal muscle. Ionescu V; Radu H; Nicolescu P Arch Pathol; 1975 Aug; 99(8):436-41. PubMed ID: 1147838 [TBL] [Abstract][Full Text] [Related]
28. [Status of connective tissue in progressive muscular dystrophies]. Sitnikov VF; Temin PA Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(3):272-6. PubMed ID: 442894 [TBL] [Abstract][Full Text] [Related]
29. Capillaries of human overacting extraocular muscles. Ludatscher RM; Meyer E; Zonis S; Lichtig C Invest Ophthalmol Vis Sci; 1984 Dec; 25(12):1441-7. PubMed ID: 6511227 [TBL] [Abstract][Full Text] [Related]
30. Intramuscular renin-angiotensin system is activated in human muscular dystrophy. Sun G; Haginoya K; Dai H; Chiba Y; Uematsu M; Hino-Fukuyo N; Onuma A; Iinuma K; Tsuchiya S J Neurol Sci; 2009 May; 280(1-2):40-8. PubMed ID: 19232644 [TBL] [Abstract][Full Text] [Related]
31. Electron microscopic study on the satellite cell in the muscle of Duchenne muscular dystrophy. Wakayama Y J Neuropathol Exp Neurol; 1976; 35(5):532-40. PubMed ID: 956871 [TBL] [Abstract][Full Text] [Related]
32. Considerations about a possible role played by connective tissue proliferation and vascular disturbances in the pathogenesis of progressive muscular dystrophy. Cazzato G Eur Neurol; 1968; 1(3):158-79. PubMed ID: 5698619 [No Abstract] [Full Text] [Related]
33. [Expression of connective tissue growth factor in progressive muscular dystrophy]. Sun GL; Yao F; Jiang HK; Li P; Kazuhiro H Zhonghua Er Ke Za Zhi; 2005 Oct; 43(10):753-7. PubMed ID: 16255854 [TBL] [Abstract][Full Text] [Related]
34. Ultrastructural abnormalities in muscular vessels of hyperthyroid patients. Finol HJ; Müller B; Torres SH; Domínguez JJ; Perdomo P; Montes de Oca I Acta Neuropathol; 1986; 71(1-2):64-9. PubMed ID: 3776475 [TBL] [Abstract][Full Text] [Related]
35. Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency. Niiyama T; Higuchi I; Hashiguchi T; Suehara M; Uchida Y; Horikiri T; Shiraishi T; Saitou A; Hu J; Nakagawa M; Arimura K; Osame M Acta Neuropathol; 2003 Aug; 106(2):137-42. PubMed ID: 12736748 [TBL] [Abstract][Full Text] [Related]
36. Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses. Côté PD; Moukhles H; Lindenbaum M; Carbonetto S Nat Genet; 1999 Nov; 23(3):338-42. PubMed ID: 10610181 [TBL] [Abstract][Full Text] [Related]
37. [Ultrastructural observations on 24 cases of pseudo-hypertrophic muscular dystrophy]. Hang ZB; Luo DR; Wu KM Zhonghua Bing Li Xue Za Zhi; 1994; 23(3):159-61. PubMed ID: 7954955 [TBL] [Abstract][Full Text] [Related]
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39. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease? Taniguchi M; Kurahashi H; Noguchi S; Sese J; Okinaga T; Tsukahara T; Guicheney P; Ozono K; Nishino I; Morishita S; Toda T Biochem Biophys Res Commun; 2006 Apr; 342(2):489-502. PubMed ID: 16487936 [TBL] [Abstract][Full Text] [Related]
40. Intramuscular capillary abnormalities in a case of myotonic dystrophy (Steinert's disease). Finol H; Torres S; Rabucha A; Saenz H Acta Cient Venez; 1992; 43(5):284-9. PubMed ID: 1343740 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]