BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 308614)

  • 1. Systemic membrane defect in the proximal muscular dystrophies.
    Pickard NA; Gruemer HD; Verrill HL; Isaacs ER; Robinow M; Nance WE; Myers EC; Goldsmith B
    N Engl J Med; 1978 Oct; 299(16):841-6. PubMed ID: 308614
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Possibility of prenatal diagnosis of progressive muscular dystrophy: evaluation of creatine kinase activity in serum and the capping of lymphocytes].
    Venturoli A; Sensi A; Baricordi R; Artioli A; Osti L; Mari R; Ferroni G; Lucci M
    Boll Soc Ital Biol Sper; 1983 Dec; 59(12):1988-94. PubMed ID: 6608363
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lymphocyte capping in limb-girdle muscular dystrophy: patients and carriers in an Amish isolate.
    Bader PI; Bender CJ; Creason MT; Conn PS; Townsend DW
    Am J Med Genet; 1982 Jul; 12(3):255-69. PubMed ID: 7114089
    [No Abstract]   [Full Text] [Related]  

  • 4. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP; Pegoraro E; Scacheri P; Burns RG; Taber JW; Weiss L; Spiro A; Blattner P
    Am J Med Genet; 1996 Jun; 63(4):573-80. PubMed ID: 8826437
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The contribution of assays for lymphocyte capping and creatine kinase to detection of the Becker-type dystrophy trait.
    Goldsmith BM; Gruemer HD; Hawley RJ; Pickard NA; Verrill HL; Nance WE; Miller G; Crawford RG
    Clin Chem; 1980 May; 26(6):754-9. PubMed ID: 7371153
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human lymphocyte capping and the effect of lanthanum in Duchenne muscular dystrophy.
    Horenstein AL; Emery AE
    Res Commun Chem Pathol Pharmacol; 1983 Aug; 41(2):303-12. PubMed ID: 6635321
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lymphocyte capping in limb-girdle muscular dystrophy.
    Sybert VP
    Am J Med Genet; 1983 May; 15(1):181-3. PubMed ID: 6859123
    [No Abstract]   [Full Text] [Related]  

  • 8. Dystrophin assay in muscular dystrophies: an Indian experience.
    Jain S; Sarkar C; Dinda AK; Maheshwari MC
    Natl Med J India; 1993; 6(6):259-62. PubMed ID: 7950930
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C
    Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sporadic Duchenne muscular dystrophy in females; genetic counseling of women with pelvifemoral muscular dystrophy.
    Zellweger H; Ionasescu V; Simpson J
    Helv Paediatr Acta; 1980 Sep; 35(4):343-8. PubMed ID: 7451237
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC; Gedeon AK; Haan EA; Sheffield LJ; White SJ; Bates LJ; Robertson EF; Sutherland GR
    Aust Paediatr J; 1988; 24 Suppl 1():92-7. PubMed ID: 3202740
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lymphocyte capping in carriers of Duchenne muscular dystrophy.
    Bader PI
    N Engl J Med; 1979 Sep; 301(13):725. PubMed ID: 481472
    [No Abstract]   [Full Text] [Related]  

  • 13. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection.
    Tangorra A; Curatola G; Milani-Comparetti M; Ferretti G
    Am J Med Genet; 1989 Apr; 32(4):540-4. PubMed ID: 2774000
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.
    Norman A; Harper P
    Clin Genet; 1989 Jul; 36(1):31-7. PubMed ID: 2766561
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females.
    Zatz M; Marie SK; Cerqueira A; Vainzof M; Pavanello RC; Passos-Bueno MR
    Am J Med Genet; 1998 May; 77(2):155-61. PubMed ID: 9605290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Potential pitfalls in using DNA probes to counsel Duchenne and Becker muscular dystrophy families.
    Shi YJ; Fischbeck KH; Ritter A
    Chin Med J (Engl); 1992 Jun; 105(6):469-75. PubMed ID: 1451547
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [In vitro study of fibroblasts from patients with Duchenne muscular dystrophy. Evaluation of capping and ultrastructural aspect].
    Charbonné F; Perissel B; Boué A; Normand B; Mage G; Vanneuville G; Turchini JP; Malet P
    Pathol Biol (Paris); 1985 Sep; 33(7):751-7. PubMed ID: 3909073
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lymphocyte capping in Duchenne muscular dystrophy.
    Pickard NA; Gruemer HD; Nance WE; Goldsmith BM
    Lancet; 1979 Aug; 2(8137):306. PubMed ID: 88637
    [No Abstract]   [Full Text] [Related]  

  • 19. Lymphocyte capping and carrier detection in Duchenne muscular dystrophy.
    Sands ME; Harris R
    Lancet; 1979 Sep; 2(8144):698. PubMed ID: 90790
    [No Abstract]   [Full Text] [Related]  

  • 20. Carrier detection by microsatellite analysis of Duchenne/Becker muscular dystrophy in Hungarian families.
    Bachrati CZ; Somodi Z; Endreffy E; Kalmár T; Raskó I
    Ann Hum Genet; 1998 Nov; 62(Pt 6):511-20. PubMed ID: 10363129
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.