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26. Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency. Villanova M; Malandrini A; Biancotti R; Löfgren A; Mongini T; Six J; Salvestroni R; Parrotta E; Van Broeckhoven C; Paolozzi C; Guazzi G Neuromuscul Disord; 1996 May; 6(3):167-72. PubMed ID: 8784804 [TBL] [Abstract][Full Text] [Related]
27. Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy. Nicholson LV; Johnson MA; Bushby KM; Gardner-Medwin D Arch Dis Child; 1993 May; 68(5):632-6. PubMed ID: 8323331 [TBL] [Abstract][Full Text] [Related]
28. Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness. Sewry CA; Sansome A; Clerk A; Sherratt TG; Hasson N; Rodillo E; Heckmatt JZ; Strong PN; Dubowitz V Neuromuscul Disord; 1993 Mar; 3(2):141-8. PubMed ID: 8358239 [TBL] [Abstract][Full Text] [Related]
29. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. Shomrat R; Gluck E; Legum C; Shiloh Y Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727 [TBL] [Abstract][Full Text] [Related]
30. Cardiac involvement in a family with Becker muscular dystrophy. Yu Y; Yamabe H; Fujita H; Inoue T; Yokota Y; Nishio H; Wada H; Matsuo M; Yokoyama M Intern Med; 1995 Sep; 34(9):919-23. PubMed ID: 8580570 [TBL] [Abstract][Full Text] [Related]
31. Very small dystrophin molecule in a family with a mild form of Becker dystrophy. Morandi L; Mora M; Bernasconi P; Mantegazza R; Gebbia M; Balestrini MR; Cornelio F Neuromuscul Disord; 1993 Jan; 3(1):65-70. PubMed ID: 8329891 [TBL] [Abstract][Full Text] [Related]
32. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers. Sumita DR; Vainzof M; Campiotto S; Cerqueira AM; Cánovas M; Otto PA; Passos-Bueno MR; Zatz M Am J Med Genet; 1998 Dec; 80(4):356-61. PubMed ID: 9856563 [TBL] [Abstract][Full Text] [Related]
33. Dystrophin analysis in Duchenne and Becker muscular dystrophy carriers: correlation with intracellular calcium and albumin. Morandi L; Mora M; Gussoni E; Tedeschi S; Cornelio F Ann Neurol; 1990 Nov; 28(5):674-9. PubMed ID: 1979724 [TBL] [Abstract][Full Text] [Related]
34. Diagnosis of DMD carrier status in a family with no known affected males. Muntoni F; Mateddu A; Cau M; Congiu R; Puddu R; Cossu P; Cao A; Melis MA Dev Med Child Neurol; 1993 Jan; 35(1):70-3. PubMed ID: 8095479 [TBL] [Abstract][Full Text] [Related]
35. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage. Rose MR; Howard RS; Genet SA; McMahon CJ; Whitfield A; Morgan-Hughes JA Muscle Nerve; 1993 Jan; 16(1):57-62. PubMed ID: 8423832 [TBL] [Abstract][Full Text] [Related]
36. Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females. Pegoraro E; Schimke RN; Arahata K; Hayashi Y; Stern H; Marks H; Glasberg MR; Carroll JE; Taber JW; Wessel HB Am J Hum Genet; 1994 Jun; 54(6):989-1003. PubMed ID: 8198142 [TBL] [Abstract][Full Text] [Related]
37. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies]. Tuffery-Giraud S; Chambert S; Demaille J; Claustres M Ann Biol Clin (Paris); 1999; 57(4):417-26. PubMed ID: 10432364 [TBL] [Abstract][Full Text] [Related]
38. The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol. van Essen AJ; Kneppers AL; van der Hout AH; Scheffer H; Ginjaar IB; ten Kate LP; van Ommen GJ; Buys CH; Bakker E J Med Genet; 1997 Oct; 34(10):805-12. PubMed ID: 9350811 [TBL] [Abstract][Full Text] [Related]