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.
25. [Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]. Bonilla E; Minetti C; Chang HW; Medori R; Cordone G; Di Mauro S Minerva Pediatr; 1991 Mar; 43(3):67-70. PubMed ID: 1870528 [No Abstract] [Full Text] [Related]
26. [[Study of dystrophin in muscular dystrophy--why and when?]. Sariola H; Koistinen H; Wallgren-Pettersson C; Rapola J Duodecim; 1992; 108(6):591-6. PubMed ID: 1366119 [No Abstract] [Full Text] [Related]
27. [Development of an ultrasound-mediated nucleic acid delivery system for treating muscular dystrophies]. Negishi Y; Hamano N; Shiono H; Akiyama S; Endo-Takahashi Y; Suzuki R; Maruyama K; Aramaki Y Yakugaku Zasshi; 2012; 132(12):1383-8. PubMed ID: 23208045 [TBL] [Abstract][Full Text] [Related]
29. [Duchenne muscular dystrophy]. Ishiura S; Sugita H No To Shinkei; 1991 May; 43(5):405-9. PubMed ID: 1910927 [No Abstract] [Full Text] [Related]
30. Etiology and pathogenesis of the muscular dystrophies. Van den Bergh PY; Tomé FM; Fardeau M Acta Neurol Belg; 1995; 95(3):123-41. PubMed ID: 7484050 [TBL] [Abstract][Full Text] [Related]
31. [Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations]. Gold R; Kress W; Meurers B; Müller CR; Reichmann H Nervenarzt; 1991 Jun; 62(6):360-8. PubMed ID: 1876220 [No Abstract] [Full Text] [Related]
35. Human molecular genetics and the elucidation of the primary biochemical defect in Duchenne muscular dystrophy. Hoffman EP Cell Motil Cytoskeleton; 1989; 14(1):163-8. PubMed ID: 2684423 [No Abstract] [Full Text] [Related]
36. Genetic medicine and the muscular dystrophies: triumphs and tribulations. Hoffman EP; Chen YW Dev Med Child Neurol; 2002 Feb; 44(2):136-40. PubMed ID: 11848111 [No Abstract] [Full Text] [Related]
37. Detection of gene deletions by PCR analysis in a Malaysian patient with Duchenne muscular dystrophy. Lee MK; Manonmani V; Arahata K Med J Malaysia; 1993 Mar; 48(1):46-50. PubMed ID: 8341171 [TBL] [Abstract][Full Text] [Related]
38. [Neuromuscular diseases. Molecular genetic methods will revolutionize diagnosis and treatment]. Anvret M; Edström L; Ahlberg G Lakartidningen; 1992 Mar; 89(11):862, 865-9. PubMed ID: 1545641 [No Abstract] [Full Text] [Related]
39. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)]. Lukás Z; Vojtísková M; Fajkusová L; Bednarík J; Kadanka Z; Hájek J; Hermanová M; Vohánka S; Vytopil M Cesk Patol; 2001 Nov; 37(4):137-45. PubMed ID: 11813630 [TBL] [Abstract][Full Text] [Related]