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Journal Abstract Search

436 related items for PubMed ID: 12609097

  • 1. Familial Wolff-Parkinson-White syndrome is linked to the loci on chromosome 7q3.
    Liu W, Liu G, Hu D, Qi Y, Shan Z, Yang D, Liu D, Wang Y.
    Chin Med J (Engl); 2002 Nov; 115(11):1733-5. PubMed ID: 12609097
    [Abstract] [Full Text] [Related]

  • 2. Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.
    MacRae CA, Ghaisas N, Kass S, Donnelly S, Basson CT, Watkins HC, Anan R, Thierfelder LH, McGarry K, Rowland E.
    J Clin Invest; 1995 Sep; 96(3):1216-20. PubMed ID: 7657794
    [Abstract] [Full Text] [Related]

  • 3. [Association between pre-excitation syndrome and 7q3 D7S505 pseudonym gene].
    Liu W, Liu G, Hu D, Qi Y, Shan Z, Luo L, Zhang M, Wang L, Yi J.
    Zhonghua Yi Xue Za Zhi; 2002 Jun 25; 82(12):820-3. PubMed ID: 12126529
    [Abstract] [Full Text] [Related]

  • 4. Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.
    Mehdirad AA, Fatkin D, DiMarco JP, MacRae CA, Wase A, Seidman JG, Seidman CE, Benson DW.
    J Cardiovasc Electrophysiol; 1999 May 25; 10(5):629-35. PubMed ID: 10355918
    [Abstract] [Full Text] [Related]

  • 5. [Heredity in Wolff-Parkinson-White syndrome].
    Fomina IG, Logunova LV, Pogrebkova NS.
    Klin Med (Mosk); 1990 Apr 25; 68(4):61-6. PubMed ID: 2370785
    [Abstract] [Full Text] [Related]

  • 6. [Familial occurrence of the Wolff-Parkinson-White (WPW) syndrome].
    Homola D, Srnová V.
    Vnitr Lek; 1968 Sep 25; 14(9):850-6. PubMed ID: 5680885
    [No Abstract] [Full Text] [Related]

  • 7. [Inheritance of Wolff-Parkinson-White syndrome and evolution of its clinical symptoms in families of patients in a prospective trial].
    Fomina IG, Logunova LV, Kuleshov NP, Markova ZS.
    Klin Med (Mosk); 2001 Sep 25; 79(3):26-30. PubMed ID: 11490411
    [Abstract] [Full Text] [Related]

  • 8. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.
    Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, Ali Hassan AS, Ahmad F, Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R.
    N Engl J Med; 2001 Jun 14; 344(24):1823-31. PubMed ID: 11407343
    [Abstract] [Full Text] [Related]

  • 9. High risk of sudden death associated with a PRKAG2-related familial Wolff-Parkinson-White syndrome.
    Zhang LP, Hui B, Gao BR.
    J Electrocardiol; 2011 Jun 14; 44(4):483-6. PubMed ID: 20381067
    [Abstract] [Full Text] [Related]

  • 10. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC.
    Arch Neurol; 2007 Nov 14; 64(11):1625-7. PubMed ID: 17998445
    [Abstract] [Full Text] [Related]

  • 11. Is Wolff-Parkinson-White syndrome a genetic disease?
    Ehtisham J, Watkins H.
    J Cardiovasc Electrophysiol; 2005 Nov 14; 16(11):1258-62. PubMed ID: 16302915
    [Abstract] [Full Text] [Related]

  • 12. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
    [Abstract] [Full Text] [Related]

  • 13. Mutation of the MYH7 gene in a child with hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome.
    Bobkowski W, Sobieszczańska M, Turska-Kmieć A, Nowak A, Jagielski J, Gonerska M, Lebioda A, Siwińska A.
    J Appl Genet; 2007 Feb 26; 48(2):185-8. PubMed ID: 17495353
    [Abstract] [Full Text] [Related]

  • 14. [Familial WPW syndrome].
    Homola D, Vrba M, Srnová V.
    Vnitr Lek; 1982 Jan 26; 28(1):53-60. PubMed ID: 7058638
    [No Abstract] [Full Text] [Related]

  • 15. [Cardiogenetic studies. Familial occurrence of Wolff-Parkinson-White syndrome].
    Pedich W.
    Pol Tyg Lek; 1969 Aug 11; 24(32):1232-4. PubMed ID: 5351569
    [No Abstract] [Full Text] [Related]

  • 16. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
    Ye X, Shi L, Yin W, Meng L, Wang QK, Bian Z.
    J Clin Periodontol; 2009 Aug 11; 36(8):627-33. PubMed ID: 19552635
    [Abstract] [Full Text] [Related]

  • 17. [Does patient age influence the indications for investigating asympatomatic Wolff-Parkinson-White syndrome?].
    Brembilla-Perrot B, Holban I, Houriez P, Beurrier D, Claudon O, Vançon AC.
    Arch Mal Coeur Vaiss; 2000 Dec 11; 93(12):1523-7. PubMed ID: 11211447
    [Abstract] [Full Text] [Related]

  • 18. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 11; 152(1):29-36. PubMed ID: 15656797
    [Abstract] [Full Text] [Related]

  • 19. Proximal trisomy of 1q mosaicism in a girl with hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome and multiple congenital anomalies.
    Hirshfeld AB, Thompson WR, Patel A, Boone LB, Murphy AM.
    Am J Med Genet; 2001 May 15; 100(4):264-8. PubMed ID: 11343316
    [Abstract] [Full Text] [Related]

  • 20. [Familial Wolff-Parkinson-White syndrome].
    Montemurro G, D'Avino R, Miraldi C.
    Boll Soc Ital Cardiol; 1967 May 15; 12(5):384-7. PubMed ID: 5606883
    [No Abstract] [Full Text] [Related]

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