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 *

150 related articles for article (PubMed ID: 37301765)

  • 21. Guidelines for the diagnosis and management of hypertrophic cardiomyopathy.
    Semsarian C;
    Heart Lung Circ; 2011 Nov; 20(11):688-90. PubMed ID: 22000299
    [No Abstract]   [Full Text] [Related]  

  • 22. [Familial hypertrophic cardiomyopathy--a case report].
    Domal-Kwiatkowska D; Glanowska G; Smolik S; Wilczewski P; Mazurek U; Nowalany-Kozielska E; Fudal M; Wodniecki J
    Kardiol Pol; 2006 Nov; 64(11):1287-91. PubMed ID: 17165166
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [A Chinese pedigree with hypertrophic cardiomyopathy caused by rare homozygous mutation of TNNI3 gene p.Arg162Gln].
    Duan LQ; Li Q; Ren Y; Xu JR; Han QH
    Zhonghua Xin Xue Guan Bing Za Zhi; 2019 Dec; 47(12):1008-1010. PubMed ID: 31877599
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Factors Associated with Uptake of Genetics Services for Hypertrophic Cardiomyopathy.
    Khouzam A; Kwan A; Baxter S; Bernstein JA
    J Genet Couns; 2015 Oct; 24(5):797-809. PubMed ID: 25566741
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations: prediction of clinical status--is molecular genetics a new tool for the management of hypertrophic cardiomyopathy in clinical practice?
    Hengstenberg C; Erdmann J; Charron P
    Cardiovasc Res; 2003 Feb; 57(2):298-301. PubMed ID: 12566102
    [No Abstract]   [Full Text] [Related]  

  • 26. Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene.
    Hallıoğlu Kılınç O; Giray D; Bişgin A; Tuğ Bozdoğan S; Karpuz D
    Turk Kardiyol Dern Ars; 2017 Jul; 45(5):450-453. PubMed ID: 28694399
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Primary prevention of sudden cardiac death in a low-risk child with familial hypertrophic cardiomyopathy: the role of cardiac magnetic resonance imaging.
    Yamazawa H; Takeda A; Takei K; Furukawa T
    Clin Res Cardiol; 2014 Jan; 103(1):75-7. PubMed ID: 24170035
    [No Abstract]   [Full Text] [Related]  

  • 28. A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.
    Fokstuen S; Lyle R; Munoz A; Gehrig C; Lerch R; Perrot A; Osterziel KJ; Geier C; Beghetti M; Mach F; Sztajzel J; Sigwart U; Antonarakis SE; Blouin JL
    Hum Mutat; 2008 Jun; 29(6):879-85. PubMed ID: 18409188
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Looking for hypertrophic cardiomyopathy in the community: why is it important?
    Nistri S; Olivotto I; Girolami F; Torricelli F; Cecchi F; Yacoub MH
    J Cardiovasc Transl Res; 2009 Dec; 2(4):392-7. PubMed ID: 20559997
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Sarcomere gene mutations--a cause of hypertrophic cardiomyopathy].
    Kuusisto J; Jääskeläinen P; Laakso M
    Duodecim; 1999; 115(9):997-8. PubMed ID: 11877825
    [No Abstract]   [Full Text] [Related]  

  • 31. [Malignant form of familial hypertrophic cardiomyopathy complicated with ventricular fibrillation in siblings. Electrocardiogram in hypertrophic cardiomyopathy - a review].
    Kukla P; Petkow-Dimitrow P; Jastrzebski M; Bednarek J; Lelakowski J; Bryniarski L
    Kardiol Pol; 2009 Jul; 67(7):774-80; discussion 781. PubMed ID: 19650001
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic Correlation.
    Frustaci A; De Luca A; Guida V; Biagini T; Mazza T; Gaudio C; Letizia C; Russo MA; Galea N; Chimenti C
    J Am Heart Assoc; 2018 Feb; 7(4):. PubMed ID: 29440008
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recent progress in the genetics of cardiomyopathy and its role in the clinical evaluation of patients with cardiomyopathy.
    Ghosh N; Haddad H
    Curr Opin Cardiol; 2011 Mar; 26(2):155-64. PubMed ID: 21297463
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Diagnostic evaluation of hypertrophic cardiomyopathy in its clinical and preclinical phases.
    Mattos BP; Torres MA; Freitas VC
    Arq Bras Cardiol; 2008 Jul; 91(1):51-62. PubMed ID: 18660946
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes.
    Rosenzweig A; Watkins H; Hwang DS; Miri M; McKenna W; Traill TA; Seidman JG; Seidman CE
    N Engl J Med; 1991 Dec; 325(25):1753-60. PubMed ID: 1944483
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Age-dependent heterogeneity of familiar hypertrophic cardiomyopathy phenotype: a role of cardiovascular magnetic resonance.
    Glaveckaitė S; Rudys A; Mikštienė V; Valevičienė N; Palionis D; Laucevičius A
    Medicina (Kaunas); 2013; 49(9):422-5. PubMed ID: 24589579
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy].
    Pan GZ; Liu WL; Hu DY; Xie WL; Zhu TG; Li L; Li CL; Bian H
    Zhonghua Yi Xue Za Zhi; 2006 Nov; 86(42):2998-3001. PubMed ID: 17288815
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [The clinical characteristics of 5 patients with inherited hypertrophic cardiomyopathy].
    He JQ; Han ZH; Ren XJ; Gao YC; Zhang XL; Jiang TY
    Zhonghua Xin Xue Guan Bing Za Zhi; 2009 Apr; 37(4):320-3. PubMed ID: 19791467
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Familial hypertrophic cardiomyopathy complicated by complete atrioventricular block.
    Cicek D; Camsari A; Doven O
    Acta Cardiol; 2004 Feb; 59(1):71-4. PubMed ID: 15030138
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A contemporary approach to hypertrophic cardiomyopathy.
    Ho CY; Seidman CE
    Circulation; 2006 Jun; 113(24):e858-62. PubMed ID: 16785342
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.