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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 10322668)

  • 41. The cardiac troponin I gene is not associated with hypertrophic cardiomyopathy in patients from eastern Finland.
    Jääskeläinen P; Miettinen R; Silvennoinen K; Vauhkonen I; Laakso M; Kuusisto J
    J Mol Cell Cardiol; 1999 Nov; 31(11):2031-6. PubMed ID: 10591029
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Hypertrophic cardiomyopathy and HLA.
    Bloch A; Crittin J; Barras C; Jeannet M
    N Engl J Med; 1980 May; 302(18):1033. PubMed ID: 7189243
    [No Abstract]   [Full Text] [Related]  

  • 43. Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy.
    Cuda G; Mussari A; Concolino D; Costanzo FS; Strisciuglio P
    Hum Mutat; 2002 Mar; 19(3):309-10. PubMed ID: 11857753
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Hypertrophic cardiomyopathy: from diagnosis to prevention].
    Hassink RJ; Grosfeld MJ; Marcelis C; Delhaas T; Doevendans PA
    Ned Tijdschr Geneeskd; 2003 Jun; 147(24):1181-4. PubMed ID: 12845840
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Novel cardiac beta-myosin heavy chain gene missense mutations (R869C and R870C) that cause familial hypertrophic cardiomyopathy.
    Anan R; Shono H; Tei C
    Hum Mutat; 2000 Jun; 15(6):584. PubMed ID: 10862102
    [No Abstract]   [Full Text] [Related]  

  • 46. Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.
    Van Driest SL; Jaeger MA; Ommen SR; Will ML; Gersh BJ; Tajik AJ; Ackerman MJ
    J Am Coll Cardiol; 2004 Aug; 44(3):602-10. PubMed ID: 15358028
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Bilateral neurogenic osteoarthropathy in a case of syringomyelia associated with familial hypertrophic obstructive cardiomyopathy].
    Lucci B
    Riv Neurobiol; 1979; 25(3):352-61. PubMed ID: 263616
    [No Abstract]   [Full Text] [Related]  

  • 48. Hypertrophic cardiomyopathy in a Portuguese population: mutations in the myosin-binding protein C gene.
    Cardim N; Perrot A; Santos S; Morgado P; Pádua M; Ferreira S; Reis RP; Monteiro C; Ferreira T; Correia JM; Osterziel KJ
    Rev Port Cardiol; 2005 Dec; 24(12):1463-76. PubMed ID: 16566405
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Familial hypertrophic cariomyopathy and lentiginosis.
    Hopkins BE; Taylor RR; Robinson JS
    Aust N Z J Med; 1975 Aug; 5(4):359-64. PubMed ID: 1058676
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Diagnostic value of abnormal Q waves for identification of preclinical carriers of hypertrophic cardiomyopathy based on a molecular genetic diagnosis.
    Konno T; Shimizu M; Ino H; Yamaguchi M; Terai H; Uchiyama K; Oe K; Mabuchi T; Kaneda T; Mabuchi H
    Eur Heart J; 2004 Feb; 25(3):246-51. PubMed ID: 14972426
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
    Doolan A; Tebo M; Ingles J; Nguyen L; Tsoutsman T; Lam L; Chiu C; Chung J; Weintraub RG; Semsarian C
    J Mol Cell Cardiol; 2005 Feb; 38(2):387-93. PubMed ID: 15698845
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel missense mutation (R712L) adjacent to the "active thiol" region of the cardiac beta-myosin heavy chain gene causing hypertrophic cardiomyopathy in an Indian family.
    Sakthivel S; Joseph PK; Tharakan JM; Vosberg HP; Rajamanickam C
    Hum Mutat; 2000 Mar; 15(3):298-9. PubMed ID: 10679957
    [No Abstract]   [Full Text] [Related]  

  • 53. [Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].
    García-Castro M; Coto E; Reguero JR; Berrazueta JR; Alvarez V; Alonso B; Sainz R; Martín M; Morís C
    Rev Esp Cardiol; 2009 Jan; 62(1):48-56. PubMed ID: 19150014
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Familial cardiomyopathy: a clinical, hemodynamic and angiographic study in one family.
    Barold SS; Linhart JW; Hildner FJ; Rywlin A; Samet P
    Chest; 1970 Feb; 57(2):141-7. PubMed ID: 5460840
    [No Abstract]   [Full Text] [Related]  

  • 55. [Instability of alpha-2-macroglobulin protease complex in familial cardiomyopathy].
    Csanády M; Szász K; Lózsa A
    Orv Hetil; 1979 Mar; 120(11):635-40. PubMed ID: 86178
    [No Abstract]   [Full Text] [Related]  

  • 56. Coagulation and platelet function in hypertrophic cardiomyopathy.
    Longo G; Cecchi F; Grossi A; Matucci M; Rafanelli D; Vannucchi AM; Casprini P; Vannini S; Morfini M; Dolara A
    Thromb Haemost; 1984 Apr; 51(2):299. PubMed ID: 6539961
    [No Abstract]   [Full Text] [Related]  

  • 57. [Hypertrophic myocardiopathy and HLA (author's transl)].
    Pareja E; Valverde MD; Garrido F; Pasalodos-Pita J; Sancho Galdón M; Kindelan JM; Collado A; Sánchez Guijo P
    Sangre (Barc); 1981; 26(1):58-64. PubMed ID: 7196093
    [No Abstract]   [Full Text] [Related]  

  • 58. [Genetic investigations in functional obstructive subvalvular aortic stenosis (irregular hypertrophic cardiomyopathy)].
    Jörgensen G
    Humangenetik; 1968; 6(1):13-28. PubMed ID: 5749048
    [No Abstract]   [Full Text] [Related]  

  • 59. [The molecular basis of familial hypertrophic cardiomyopathy].
    Sánchez Cascos A
    Rev Esp Cardiol; 1991 Apr; 44(4):288. PubMed ID: 2068375
    [No Abstract]   [Full Text] [Related]  

  • 60. [Familial paroxysmal ataxia].
    Ramo Tello C; González JL; Hernández Gallego J; Calandre L; Bermejo F
    Neurologia; 1986; 1(5):212-5. PubMed ID: 3274218
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.