137 related articles for article (PubMed ID: 1525558)
1. Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining.
Chevron MP; Tuffery S; Echenne B; Demaille J; Claustres M
Neuromuscul Disord; 1992; 2(1):47-50. PubMed ID: 1525558
[TBL] [Abstract][Full Text] [Related]
2. Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.
Voit T; Stuettgen P; Cremer M; Goebel HH
Neuropediatrics; 1991 Aug; 22(3):152-62. PubMed ID: 1944822
[TBL] [Abstract][Full Text] [Related]
3. Is dystrophin labelling always discontinuous in Becker muscular dystrophy?
Slater CR; Nicholson LV
J Neurol Sci; 1991 Feb; 101(2):187-92. PubMed ID: 2033404
[TBL] [Abstract][Full Text] [Related]
4. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages.
Vainzof M; Pavanello RC; Pavanello I; Tsanaclis AM; Levy JA; Passos-Bueno MR; Rapaport D; Zatz M
Neuromuscul Disord; 1991; 1(3):177-83. PubMed ID: 1822792
[TBL] [Abstract][Full Text] [Related]
5. A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidence.
Augier N; Boucraut J; Léger J; Anoal M; Nicholson LV; Voelkel MA; Léger JJ; Pellissier JF
J Neurol Sci; 1992 Feb; 107(2):233-8. PubMed ID: 1564523
[TBL] [Abstract][Full Text] [Related]
6. Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.
Haginoya K; Yamamoto K; Iinuma K; Yanagisawa T; Ichinohasama Y; Shimmoto M; Suzuki Y; Tada K
J Neurol; 1991 Oct; 238(7):375-8. PubMed ID: 1683669
[TBL] [Abstract][Full Text] [Related]
7. Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
Sunohara N; Arahata K; Hoffman EP; Yamada H; Nishimiya J; Arikawa E; Kaido M; Nonaka I; Sugita H
Ann Neurol; 1990 Nov; 28(5):634-9. PubMed ID: 2260849
[TBL] [Abstract][Full Text] [Related]
8. Mosaic expression of two dystrophins in a boy with progressive muscular dystrophy.
Rivier F; Tuffery S; Jellali AJ; Echenne B; Mornet D; Pons F
Muscle Nerve; 1998 Oct; 21(10):1317-20. PubMed ID: 9736061
[TBL] [Abstract][Full Text] [Related]
9. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
Arahata K; Beggs AH; Honda H; Ito S; Ishiura S; Tsukahara T; Ishiguro T; Eguchi C; Orimo S; Arikawa E
J Neurol Sci; 1991 Feb; 101(2):148-56. PubMed ID: 2033400
[TBL] [Abstract][Full Text] [Related]
10. Characterisation of dystrophin in carriers of Duchenne muscular dystrophy.
Clerk A; Rodillo E; Heckmatt JZ; Dubowitz V; Strong PN; Sewry CA
J Neurol Sci; 1991 Apr; 102(2):197-205. PubMed ID: 2072119
[TBL] [Abstract][Full Text] [Related]
11. Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy.
Voit T; Neuen-Jacob E; Mahler V; Jauch A; Cremer M
Eur J Pediatr; 1992 Feb; 151(2):112-6. PubMed ID: 1537352
[TBL] [Abstract][Full Text] [Related]
12. Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects.
Mizuno Y; Nonaka I; Hirai S; Ozawa E
J Neurol Sci; 1993 Oct; 119(1):43-52. PubMed ID: 8246010
[TBL] [Abstract][Full Text] [Related]
13. Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin.
Hori S; Ohtani S; Shimizu T; Ibi T; Sahashi K; Nonaka I; Miyamoto K; Tanabe H
J Neurol Sci; 1994 Feb; 121(2):183-9. PubMed ID: 8158213
[TBL] [Abstract][Full Text] [Related]
14. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
Gold R; Kress W; Meurers B; Meng G; Reichmann H; Müller CR
Muscle Nerve; 1992 Feb; 15(2):214-8. PubMed ID: 1549142
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
Vainzof M; Takata RI; Passos-Bueno MR; Pavanello RC; Zatz M
Hum Mol Genet; 1993 Jan; 2(1):39-42. PubMed ID: 8490621
[TBL] [Abstract][Full Text] [Related]
17. Asymptomatic Becker muscular dystrophy: expression of dystrophin and dystrophin-related protein.
Tachi N; Wakai S; Watanabe Y; Ohya K; Chiba S
Pediatr Neurol; 1993; 9(3):207-9. PubMed ID: 8352853
[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]
19. PCR and immunoblot analyses of dystrophin in Becker muscular dystrophy.
Uchino M; Miike T; Iwashita H; Uyama E; Yoshioka K; Sugino S; Ando M
J Neurol Sci; 1994 Jul; 124(2):225-9. PubMed ID: 7964876
[TBL] [Abstract][Full Text] [Related]
20. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.
Bonilla E; Schmidt B; Samitt CE; Miranda AF; Hays AP; de Oliveira AB; Chang HW; Servidei S; Ricci E; Younger DS
Am J Pathol; 1988 Dec; 133(3):440-5. PubMed ID: 3059802
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]