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295 related items for PubMed ID: 2646527

  • 1. [Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin].
    Voit T, Patel K, Sewry CA, Strong PN, Dubowitz V, Dunn MJ.
    Monatsschr Kinderheilkd; 1989 Jan; 137(1):20-7. PubMed ID: 2646527
    [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
    [Abstract] [Full Text] [Related]

  • 3. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle.
    Zubrzycka-Gaarn EE, Bulman DE, Karpati G, Burghes AH, Belfall B, Klamut HJ, Talbot J, Hodges RS, Ray PN, Worton RG.
    Nature; 1988 Jun 02; 333(6172):466-9. PubMed ID: 3287171
    [Abstract] [Full Text] [Related]

  • 4. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 02; 32(2):268-73. PubMed ID: 2648829
    [Abstract] [Full Text] [Related]

  • 5. Localization and characterization of dystrophin in muscle biopsy specimens from Duchenne muscular dystrophy and various neuromuscular disorders.
    Uchino M, Araki S, Miike T, Teramoto H, Nakamura T, Yasutake T.
    Muscle Nerve; 1989 Dec 02; 12(12):1009-16. PubMed ID: 2695839
    [Abstract] [Full Text] [Related]

  • 6. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Gilgenkrantz H, Chelly J, Récan D, Chafey P, Kaplan JC.
    C R Seances Soc Biol Fil; 1992 Dec 02; 186(4):349-53. PubMed ID: 1301222
    [Abstract] [Full Text] [Related]

  • 7. Genetic polymorphism in muscle biopsies of Duchenne and Becker muscular dystrophy patients.
    Anand A, Prabhakar S, Kaul D.
    Neurol India; 1999 Sep 02; 47(3):218-23. PubMed ID: 10514583
    [Abstract] [Full Text] [Related]

  • 8. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.
    Matsumura K, Tomé FM, Collin H, Azibi K, Chaouch M, Kaplan JC, Fardeau M, Campbell KP.
    Nature; 1992 Sep 24; 359(6393):320-2. PubMed ID: 1406935
    [Abstract] [Full Text] [Related]

  • 9. Duchenne muscular dystrophy in a girl identified by dystrophin deficiency.
    Maytal J, Shanske AL, Fox JE, Lipper S, Eviatar L.
    Neuropediatrics; 1991 Aug 24; 22(3):163-5. PubMed ID: 1944823
    [Abstract] [Full Text] [Related]

  • 10. Absence of correlation between utrophin localization and quantity and the clinical severity in Duchenne/Becker dystrophies.
    Vainzof M, Passos-Bueno MR, Man N, Zatz M.
    Am J Med Genet; 1995 Sep 25; 58(4):305-9. PubMed ID: 8533838
    [Abstract] [Full Text] [Related]

  • 11. Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodies.
    Voit T, Haas K, Léger JO, Pons F, Léger JJ.
    Am J Pathol; 1991 Nov 25; 139(5):969-76. PubMed ID: 1951635
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S, Sugino S, Ohtani Y, Matsukura M, Nishino I, Ikezawa M, Sakata A, Kondo Y, Yoshioka K, Huard J, Nonaka I, Miike T.
    Ann Neurol; 1998 Dec 25; 44(6):967-71. PubMed ID: 9851444
    [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 25; 15(2):214-8. PubMed ID: 1549142
    [Abstract] [Full Text] [Related]

  • 15. [Gene deletion analysis in molecular diagnosis of Duchenne-Becker muscular dystrophy].
    Endreffy E, László A, Kálmán M, Krenács T, Raskó I.
    Orv Hetil; 1994 Feb 20; 135(8):399-403. PubMed ID: 8139842
    [Abstract] [Full Text] [Related]

  • 16. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun 20; 21(1):151-6. PubMed ID: 9225508
    [Abstract] [Full Text] [Related]

  • 17. [Molecular genetics of Duchenne/Becker muscular dystrophy].
    Saito K, Ikeya K, Kondo E, Yamauchi A, Komine S, Fukuyama Y.
    Nihon Rinsho; 1993 Sep 20; 51(9):2420-7. PubMed ID: 8411723
    [Abstract] [Full Text] [Related]

  • 18. Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.
    Fardeau M, Matsumura K, Tomé FM, Collin H, Leturcq F, Kaplan JC, Campbell KP.
    C R Acad Sci III; 1993 Aug 20; 316(8):799-804. PubMed ID: 8044705
    [Abstract] [Full Text] [Related]

  • 19. [Cardiologic study of 10 patients with Duchenne muscular dystrophy(DMD): personal experience].
    Falsaperla R, Romeo G, Sciacca P, Di Giorgio A, Mattia CL, Distefano G.
    Pediatr Med Chir; 2001 Aug 20; 23(1):57-60. PubMed ID: 11486424
    [Abstract] [Full Text] [Related]

  • 20. Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.
    Yoshida K, Ikeda S, Nakamura A, Kagoshima M, Takeda S, Shoji S, Yanagisawa N.
    Muscle Nerve; 1993 Nov 20; 16(11):1161-6. PubMed ID: 8413368
    [Abstract] [Full Text] [Related]

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