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 *

129 related articles for article (PubMed ID: 6682724)

  • 41. The Burden of Early Phenotypes and the Influence of Wall Thickness in Hypertrophic Cardiomyopathy Mutation Carriers: Findings From the HCMNet Study.
    Ho CY; Day SM; Colan SD; Russell MW; Towbin JA; Sherrid MV; Canter CE; Jefferies JL; Murphy AM; Cirino AL; Abraham TP; Taylor M; Mestroni L; Bluemke DA; Jarolim P; Shi L; Sleeper LA; Seidman CE; Orav EJ;
    JAMA Cardiol; 2017 Apr; 2(4):419-428. PubMed ID: 28241245
    [TBL] [Abstract][Full Text] [Related]  

  • 42. First description of germline mosaicism in familial hypertrophic cardiomyopathy.
    Forissier JF; Richard P; Briault S; Ledeuil C; Dubourg O; Charbonnier B; Carrier L; Moraine C; Bonne G; Komajda M; Schwartz K; Hainque B
    J Med Genet; 2000 Feb; 37(2):132-4. PubMed ID: 10662815
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 3D echocardiographic imaging of a septal myocardial cleft in hypertrophic cardiomyopathy.
    Cagli K; Golbasi Z; Turak O; Ozeke O; Ekizler FA
    Echocardiography; 2016 Dec; 33(12):1929-1930. PubMed ID: 27659039
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.
    Posen BM; Moolman JC; Corfield VA; Brink PA
    Br Heart J; 1995 Jul; 74(1):40-6. PubMed ID: 7662452
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Asymmetric septal hypertrophy.
    Ann Intern Med; 1974 Nov; 81(5):650-80. PubMed ID: 4608574
    [No Abstract]   [Full Text] [Related]  

  • 46. An ARG403GLN beta-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy; description of clinical features of the family members.
    Conte MR; Morelio M; Mangiardi L; Orzan F; Checco L; Bonfiglio G; Alfarano A; Camaschella C; Brusca A
    Eur Heart J; 1997 Jun; 18(6):1033-4. PubMed ID: 9183600
    [No Abstract]   [Full Text] [Related]  

  • 47. Severe apical hypertrophic cardiomyopathy with Ser 236 Gly mutation in MYBPC3: A three-year follow-up investigation.
    Cen X; Zheng J; Hu X; Qu B
    Hellenic J Cardiol; 2017; 58(5):366-368. PubMed ID: 28062247
    [No Abstract]   [Full Text] [Related]  

  • 48. Can echocardiography and ECG discriminate hereditary transthyretin V30M amyloidosis from hypertrophic cardiomyopathy?
    Gustavsson S; Granåsen G; Grönlund C; Wiklund U; Mörner S; Henein M; Suhr OB; Lindqvist P
    Amyloid; 2015; 22(3):163-70. PubMed ID: 26104852
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Classification of hypertrophic cardiomyopathy by real time cross-sectional echocardiography: correlation with M-mode echocardiographic findings and clinical features (author's transl)].
    Kawanishi H; Inoh T; Yokota Y; Ohmori K; Hayakawa M; Kaku K; Kumaki T; Fukuzaki H
    J Cardiogr; 1981 Jun; 11(2):431-8. PubMed ID: 7198670
    [No Abstract]   [Full Text] [Related]  

  • 50. Left ventricular noncompaction associated with hypertrophic cardiomyopathy: echocardiographic diagnosis and genetic analysis of a new pedigree in China.
    Yuan L; Xie M; Cheng TO; Wang X; Zhu F; Kong X; Ghoorah D
    Int J Cardiol; 2014 Jun; 174(2):249-59. PubMed ID: 24698237
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Morphological quantification and differentiation of left ventricular hypertrophy in hypertrophic cardiomyopathy and hypertensive heart disease. A two dimensional echocardiographic study.
    Keller H; Wanger KC; Goepfrich M; Stegaru B; Buss J; Heene DL
    Eur Heart J; 1990 Jan; 11(1):65-74. PubMed ID: 2137778
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Familial hypertrophic cardiomyopathy].
    Wróblewska-Kałuzewska M; Ozimek W; Pleskot M; Jedrasik P
    Pol Merkur Lekarski; 1997 Feb; 2(8):129-31. PubMed ID: 9538659
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Familial spontaneous complete heart block in hypertrophic cardiomyopathy.
    Louie EK; Maron BJ
    Br Heart J; 1986 May; 55(5):469-74. PubMed ID: 3707787
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Echocardiographic assessment of left ventricular hypertrophy in patients with obstructive or nonobstructive hypertrophic cardiomyopathy.
    Maron BJ
    Eur Heart J; 1983 Nov; 4 Suppl F():73-91. PubMed ID: 6686547
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Genotype-phenotype correlation of R870H mutation in hypertrophic cardiomyopathy.
    Tanjore RR; Sikindlapuram AD; Calambur N; Thakkar B; Kerkar PG; Nallari P
    Clin Genet; 2006 May; 69(5):434-6. PubMed ID: 16650083
    [No Abstract]   [Full Text] [Related]  

  • 56. Natural history of genotype positive-phenotype negative patients with hypertrophic cardiomyopathy.
    Gray B; Ingles J; Semsarian C
    Int J Cardiol; 2011 Oct; 152(2):258-9. PubMed ID: 21862152
    [No Abstract]   [Full Text] [Related]  

  • 57. Deformation patterns in genotyped patients with hypertrophic cardiomyopathy.
    Geske JB; Bos JM; Gersh BJ; Ommen SR; Eidem BW; Ackerman MJ
    Eur Heart J Cardiovasc Imaging; 2014 Apr; 15(4):456-65. PubMed ID: 24217980
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Hypertrophic cardiomyopathy with unusual locations of left ventricular hypertrophy undetectable by M-mode echocardiography. Identification by wide-angle two-dimensional echocardiography.
    Maron BJ; Gottdiener JS; Bonow RO; Epstein SE
    Circulation; 1981 Feb; 63(2):409-18. PubMed ID: 6450004
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children.
    Greber-Platzer S; Marx M; Fleischmann C; Suppan C; Dobner M; Wimmer M
    J Mol Cell Cardiol; 2001 Jan; 33(1):141-8. PubMed ID: 11133230
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Apical hypertrophic cardiomyopathy in an adolescent.
    Abdy NA; Valdes SO; Sorrell VL; Klewer SE; Barber BJ
    Congenit Heart Dis; 2010; 5(2):182-7. PubMed ID: 20412494
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.