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.


PUBMED FOR HANDHELDS

Journal Abstract Search


121 related items for PubMed ID: 1646530

  • 1. [Duchenne's myodystrophy--a hereditary defect of the cell membranes].
    Khrennikov VIu.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):22-4. PubMed ID: 1646530
    [Abstract] [Full Text] [Related]

  • 2. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.
    Matsumura K, Campbell KP.
    Muscle Nerve; 1994 Jan; 17(1):2-15. PubMed ID: 8264699
    [Abstract] [Full Text] [Related]

  • 3. [In vitro transformation of amniotic cells to muscle cells--background and outlook].
    Streubel B, Martucci-Ivessa G, Fleck T, Bittner RE.
    Wien Med Wochenschr; 1996 Jan; 146(9-10):216-7. PubMed ID: 9012220
    [Abstract] [Full Text] [Related]

  • 4. The cardiomyopathy of Duchenne's muscular dystrophy and the function of dystrophin.
    Cziner DG, Levin RI.
    Med Hypotheses; 1993 Mar; 40(3):169-73. PubMed ID: 8502196
    [Abstract] [Full Text] [Related]

  • 5. [Screening for deletion in patients with Duchenne's myodystrophy by multiplex amplification].
    Chukhrova AL, Malygina NA, Poliakov AV, Zaĭtseva SP, Sitnikov VF, Dadali EL, Kamennykh LN, Khrennikov VIu, Badalian LO, Evgrafov OV.
    Tsitol Genet; 1994 Mar; 28(4):80-3. PubMed ID: 7801388
    [Abstract] [Full Text] [Related]

  • 6. Muscular degeneration in Duchenne's dystrophy may be caused by a mitochondrial defect.
    Lucas-Heron B.
    Med Hypotheses; 1995 Apr; 44(4):298-300. PubMed ID: 7666833
    [Abstract] [Full Text] [Related]

  • 7. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON, Puzyrev VP, Radzhabaliev ShF, Rakhmonov RA.
    Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
    [Abstract] [Full Text] [Related]

  • 8. Etiology and pathogenesis of the muscular dystrophies.
    Van den Bergh PY, Tomé FM, Fardeau M.
    Acta Neurol Belg; 1995 Oct; 95(3):123-41. PubMed ID: 7484050
    [Abstract] [Full Text] [Related]

  • 9. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs.
    Acsadi G, Dickson G, Love DR, Jani A, Walsh FS, Gurusinghe A, Wolff JA, Davies KE.
    Nature; 1991 Aug 29; 352(6338):815-8. PubMed ID: 1881437
    [Abstract] [Full Text] [Related]

  • 10. Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle.
    Ervasti JM, Ohlendieck K, Kahl SD, Gaver MG, Campbell KP.
    Nature; 1990 May 24; 345(6273):315-9. PubMed ID: 2188135
    [Abstract] [Full Text] [Related]

  • 11. Dystroglycan and muscular dystrophies related to the dystrophin-glycoprotein complex.
    Sciandra F, Bozzi M, Bianchi M, Pavoni E, Giardina B, Brancaccio A.
    Ann Ist Super Sanita; 2003 May 24; 39(2):173-81. PubMed ID: 14587215
    [Abstract] [Full Text] [Related]

  • 12. Analysis of dystrophin expression after activation of myogenesis in amniocytes, chorionic-villus cells, and fibroblasts. A new method for diagnosing Duchenne's muscular dystrophy.
    Sancho S, Mongini T, Tanji K, Tapscott SJ, Walker WF, Weintraub H, Miller AD, Miranda AF.
    N Engl J Med; 1993 Sep 23; 329(13):915-20. PubMed ID: 8361505
    [Abstract] [Full Text] [Related]

  • 13. Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?
    Matsumura K, Saito F, Yamada H, Hase A, Sunada Y, Shimizu T.
    Cell Mol Biol (Noisy-le-grand); 1999 Sep 23; 45(6):751-62. PubMed ID: 10541473
    [Abstract] [Full Text] [Related]

  • 14. [DNA and dystrophin analysis in Duchenne's and Becker's disease; benefit to the patient].
    Jennekens FG, Ippel PF.
    Ned Tijdschr Geneeskd; 1993 Jan 09; 137(2):61-3. PubMed ID: 8421528
    [No Abstract] [Full Text] [Related]

  • 15. [Membrane theory of the pathogenesis of progressive muscular dystrophy].
    Badalian LO, Temin PA, Il'in IL, Kovaleva MIu, Dzutova ED.
    Klin Med (Mosk); 1982 Oct 09; 60(10):13-6. PubMed ID: 6757558
    [No Abstract] [Full Text] [Related]

  • 16. [Clinical diagnosis of Duchenne muscular dystrophy using anti-dystrophin antibodies].
    Arahata K.
    No To Shinkei; 1991 May 09; 43(5):411-9. PubMed ID: 1910928
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.
    Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH.
    Hum Mol Genet; 2004 Sep 15; 13(18):1999-2010. PubMed ID: 15254015
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.