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4. Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin gene. Palmucci L; Doriguzzi C; Mongini T; Restagno G; Chiadò-Piat L; Maniscalco M Neurology; 1994 Mar; 44(3 Pt 1):541-3. PubMed ID: 8145928 [TBL] [Abstract][Full Text] [Related]
5. Prevalent cardiac involvement in dystrophin Becker type mutation. Siciliano G; Fanin M; Angelini C; Pollina LE; Miorin M; Saad FA; Freda MP; Muratorio A Neuromuscul Disord; 1994 Jul; 4(4):381-6. PubMed ID: 7981595 [TBL] [Abstract][Full Text] [Related]
7. Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy. Piccolo G; Azan G; Tonin P; Arbustini E; Gavazzi A; Banfi P; Mora M; Morandi L; Tedeschi S Neuromuscul Disord; 1994 Mar; 4(2):143-6. PubMed ID: 8012195 [TBL] [Abstract][Full Text] [Related]
8. 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]
13. [Post exercise myalgias as presentation form of dystrophinopathy]. Kleinsteuber K; Rocco P; Herrera L; Vainzof M; Birke ME; Yáñez M; Flandes A; Zatz M; de Carvallo P; Avaria MA Rev Med Chil; 2000 Jul; 128(7):772-7. PubMed ID: 11050839 [TBL] [Abstract][Full Text] [Related]
14. [Exercise-intolerance and exercise-induced rhabdomyolisis: etiology and diagnosis]. Laforêt P; Eymard B Rev Neurol (Paris); 2004 Feb; 160(2):217-23. PubMed ID: 15034480 [TBL] [Abstract][Full Text] [Related]
15. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation. Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344 [TBL] [Abstract][Full Text] [Related]
16. Episodic myoglobinuria in a primary gamma-sarcoglycanopathy. Pena L; Kim K; Charrow J Neuromuscul Disord; 2010 May; 20(5):337-9. PubMed ID: 20356742 [TBL] [Abstract][Full Text] [Related]
17. Mosaic pattern of dystrophins in Duchenne muscular dystrophy. Tachi N; Sasaki K; Yamada T; Imamura S; Mike T Pediatr Neurol; 1990; 6(1):54-6. PubMed ID: 2178618 [TBL] [Abstract][Full Text] [Related]
18. Dystrophin diagnosis: comparison of dystrophin abnormalities by immunofluorescence and immunoblot analyses. Arahata K; Hoffman EP; Kunkel LM; Ishiura S; Tsukahara T; Ishihara T; Sunohara N; Nonaka I; Ozawa E; Sugita H Proc Natl Acad Sci U S A; 1989 Sep; 86(18):7154-8. PubMed ID: 2674948 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]