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 *

212 related articles for article (PubMed ID: 29978770)

  • 1. Investigation of myocardial dysfunction using three-dimensional speckle tracking echocardiography in a genetic positive hypertrophic cardiomyopathy Chinese family.
    Wang J; Guo RQ; Guo JY; Zuo L; Lei CH; Shao H; Wang LF; Zhang YM; Liu LW
    Cardiol Young; 2018 Sep; 28(9):1106-1114. PubMed ID: 29978770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dual LQT1 and HCM phenotypes associated with tetrad heterozygous mutations in KCNQ1, MYH7, MYLK2, and TMEM70 genes in a three-generation Chinese family.
    Wang L; Zuo L; Hu J; Shao H; Lei C; Qi W; Liu Y; Miao Y; Ma X; Huang CL; Wang B; Zhou X; Zhang Y; Liu L
    Europace; 2016 Apr; 18(4):602-9. PubMed ID: 25825456
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Relationship between electrocardiographic and genetic mutation (MYH7-H1717Q, MYLK2-K324E and KCNQ1-R190W) phenotype in patients with hypertrophic cardiomyopathy].
    Shao H; Zhang Y; Liu L; Ma Z; Zuo L; Ye C; Wei X; Sun C; Tao L
    Zhonghua Xin Xue Guan Bing Za Zhi; 2016 Jan; 44(1):50-4. PubMed ID: 26813553
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
    Wang B; Wang J; Wang LF; Yang F; Xu L; Li WX; He Y; Zuo L; Yang QL; Shao H; Hu D; Liu LW
    Mol Med Rep; 2019 Dec; 20(6):5229-5238. PubMed ID: 31638223
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.
    Havndrup O; Bundgaard H; Andersen PS; Allan Larsen L; Vuust J; Kjeldsen K; Christiansen M
    Cardiovasc Res; 2003 Feb; 57(2):347-57. PubMed ID: 12566107
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Cumulative Effects of the MYH7-V878A and CACNA1C-A1594V Mutations in a Chinese Family with Hypertrophic Cardiomyopathy.
    Wang B; Guo RQ; Wang J; Yang F; Zuo L; Liu Y; Shao H; Ju Y; Sun C; Xu L; Zhang YM; Wang LF; Liu LW
    Cardiology; 2017; 138(4):228-237. PubMed ID: 28866666
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Myocardial Deformation Analysis in
    Höller V; Seebacher H; Zach D; Schwegel N; Ablasser K; Kolesnik E; Gollmer J; Waltl G; Rainer PP; Verheyen S; Zirlik A; Verheyen N
    Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680864
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Echocardiographic evaluation of pre-diagnostic development in young relatives genetically predisposed to hypertrophic cardiomyopathy.
    Jensen MK; Havndrup O; Christiansen M; Andersen PS; Axelsson A; Køber L; Bundgaard H
    Int J Cardiovasc Imaging; 2015 Dec; 31(8):1511-8. PubMed ID: 26231341
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical features, spectrum of causal genetic mutations and outcome of hypertrophic cardiomyopathy in South Africans.
    Ntusi NA; Shaboodien G; Badri M; Gumedze F; Mayosi BM
    Cardiovasc J Afr; 2016; 27(3):152-158. PubMed ID: 27841901
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy.
    Velicki L; Jakovljevic DG; Preveden A; Golubovic M; Bjelobrk M; Ilic A; Stojsic S; Barlocco F; Tafelmeier M; Okwose N; Tesic M; Brennan P; Popovic D; Ristic A; MacGowan GA; Filipovic N; Maier LS; Olivotto I
    BMC Cardiovasc Disord; 2020 Dec; 20(1):516. PubMed ID: 33297970
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prediction of Left Ventricular Filling Pressure by 3-Dimensional Speckle-Tracking Echocardiography in Patients With Coronary Artery Disease.
    Ma H; Xie RA; Gao LJ; Zhang JP; Wu WC; Wang H
    J Ultrasound Med; 2015 Oct; 34(10):1809-18. PubMed ID: 26333567
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Morphological and functional abnormalities pattern in hypertrophy-free HCM mutation carriers detected with echocardiography.
    Peyrou J; Réant P; Reynaud A; Cornolle C; Dijos M; Rooryck-Thambo C; Landelle M; Montaudon M; Laurent F; Roudaut R; Lafitte S
    Int J Cardiovasc Imaging; 2016 Sep; 32(9):1379-1389. PubMed ID: 27324645
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
    Revera M; van der Merwe L; Heradien M; Goosen A; Corfield VA; Brink PA; Moolman-Smook JC
    Cardiovasc Res; 2008 Mar; 77(4):687-94. PubMed ID: 18029407
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early changes in apical rotation in genotype positive children with hypertrophic cardiomyopathy mutations without hypertrophic changes on two-dimensional imaging.
    Forsey J; Benson L; Rozenblyum E; Friedberg MK; Mertens L
    J Am Soc Echocardiogr; 2014 Feb; 27(2):215-21. PubMed ID: 24325958
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three-dimensional Speckle Tracking Echocardiography in Light Chain Cardiac Amyloidosis: Examination of Left and Right Ventricular Myocardial Mechanics Parameters.
    Urbano-Moral JA; Gangadharamurthy D; Comenzo RL; Pandian NG; Patel AR
    Rev Esp Cardiol (Engl Ed); 2015 Aug; 68(8):657-64. PubMed ID: 26092748
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
    Wang J; Xu SJ; Zhou H; Wang LJ; Hu B; Fang F; Zhang XM; Luo YW; He XY; Zhuang SW; Li XM; Liu ZM; Hu DY
    Clin Cardiol; 2009 Sep; 32(9):E16-21. PubMed ID: 19645038
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy.
    Weissler-Snir A; Hindieh W; Gruner C; Fourey D; Appelbaum E; Rowin E; Care M; Lesser JR; Haas TS; Udelson JE; Manning WJ; Olivotto I; Tomberli B; Maron BJ; Maron MS; Crean AM; Rakowski H; Chan RH
    Circ Cardiovasc Imaging; 2017 Feb; 10(2):. PubMed ID: 28193612
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impact of Global and Segmental Hypertrophy on Two-Dimensional Strain Derived from Three-Dimensional Echocardiography in Hypertrophic Cardiomyopathy: Comparison with Healthy Subjects.
    Voilliot D; Huttin O; Hammache N; Filippetti L; Vaugrenard T; Aliot E; Sadoul N; Juillière Y; Selton-Suty C
    J Am Soc Echocardiogr; 2015 Sep; 28(9):1093-102. PubMed ID: 25935111
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differences of myocardial systolic deformation and correlates of diastolic function in competitive rowers and young hypertensives: a speckle-tracking echocardiography study.
    Galderisi M; Lomoriello VS; Santoro A; Esposito R; Olibet M; Raia R; Di Minno MN; Guerra G; Mele D; Lombardi G
    J Am Soc Echocardiogr; 2010 Nov; 23(11):1190-8. PubMed ID: 20810245
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
    Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
    Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.