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


395 related items for PubMed ID: 1309152

  • 1. Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry.
    Oliveira AS, Gabbai AA, Schmidt B, Kiyomoto BH, Lima JG, Minetti C, Bonilla E.
    Arq Neuropsiquiatr; 1992 Dec; 50(4):478-85. PubMed ID: 1309152
    [Abstract] [Full Text] [Related]

  • 2. [Monoclonal antibodies to dystrophin in biopsy diagnosis of Duchenne and Becker progressive muscular dystrophies].
    Lukás Z, Foretová L, Vojtísková M, Dráber P, Hájek J.
    Cesk Patol; 1994 May; 30(2):37-42. PubMed ID: 8020113
    [Abstract] [Full Text] [Related]

  • 3. Dystrophin immunostaining of muscle from Chinese patients with various neuromuscular diseases.
    Jong YJ, Chuang YH, Chen SS, Chen BH, Chiang CH.
    J Formos Med Assoc; 1991 Dec; 90(12):1143-8. PubMed ID: 1686882
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Utility of dystrophin and utrophin staining in childhood muscular dystrophy.
    Sundaram C, Vydehi B, Meena K, Murthy J.
    Indian J Pathol Microbiol; 2004 Jul; 47(3):367-9. PubMed ID: 16295426
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Dystrophin abnormality in progressive muscular dystrophy--a review article.
    Arahata K.
    Acta Paediatr Jpn; 1991 Apr; 33(2):216-21. PubMed ID: 1957648
    [Abstract] [Full Text] [Related]

  • 9. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
    Freund AA, Scola RH, Arndt RC, Lorenzoni PJ, Kay CK, Werneck LC.
    Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Immunocytochemical analysis of dystrophin in congenital muscular dystrophy.
    Arikawa E, Ishihara T, Nonaka I, Sugita H, Arahata K.
    J Neurol Sci; 1991 Sep; 105(1):79-87. PubMed ID: 1795174
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Diagnosis of dystrophinopathy by skin biopsy.
    Niiyama T, Higuchi I, Sakoda S, Matsumura T, Fukunaga H, Osame M.
    Muscle Nerve; 2002 Mar; 25(3):398-401. PubMed ID: 11870717
    [Abstract] [Full Text] [Related]

  • 18. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].
    Lukás Z, Vojtísková M, Fajkusová L, Bednarík J, Kadanka Z, Hájek J, Hermanová M, Vohánka S, Vytopil M.
    Cesk Patol; 2001 Nov; 37(4):137-45. PubMed ID: 11813630
    [Abstract] [Full Text] [Related]

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

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 20.