206 related articles for article (PubMed ID: 28427417)
1. Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome.
Chen Y; Barajas-Martinez H; Zhu D; Wang X; Chen C; Zhuang R; Shi J; Wu X; Tao Y; Jin W; Wang X; Hu D
J Transl Med; 2017 Apr; 15(1):78. PubMed ID: 28427417
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.
Fukuyama M; Wang Q; Kato K; Ohno S; Ding WG; Toyoda F; Itoh H; Kimura H; Makiyama T; Ito M; Matsuura H; Horie M
Europace; 2014 Dec; 16(12):1828-37. PubMed ID: 24728418
[TBL] [Abstract][Full Text] [Related]
4. Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia.
Bermúdez-Jiménez FJ; Carriel V; Brodehl A; Alaminos M; Campos A; Schirmer I; Milting H; Abril BÁ; Álvarez M; López-Fernández S; García-Giustiniani D; Monserrat L; Tercedor L; Jiménez-Jáimez J
Circulation; 2018 Apr; 137(15):1595-1610. PubMed ID: 29212896
[TBL] [Abstract][Full Text] [Related]
5. Identification and Functional Characterization of a Novel CACNA1C-Mediated Cardiac Disorder Characterized by Prolonged QT Intervals With Hypertrophic Cardiomyopathy, Congenital Heart Defects, and Sudden Cardiac Death.
Boczek NJ; Ye D; Jin F; Tester DJ; Huseby A; Bos JM; Johnson AJ; Kanter R; Ackerman MJ
Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1122-32. PubMed ID: 26253506
[TBL] [Abstract][Full Text] [Related]
6. Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome.
Chen Y; Barajas-Martinez H; Zhu D; Wang X; Chen C; Zhuang R; Shi J; Wu X; Tao Y; Jin W; Wang X; Hu D
J Transl Med; 2017 May; 15(1):101. PubMed ID: 28490369
[No Abstract] [Full Text] [Related]
7. Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.
Sutphin BS; Boczek NJ; Barajas-Martínez H; Hu D; Ye D; Tester DJ; Antzelevitch C; Ackerman MJ
Congenit Heart Dis; 2016 Dec; 11(6):683-692. PubMed ID: 27218670
[TBL] [Abstract][Full Text] [Related]
8. Short-term beat-to-beat variability of the QT interval is increased and correlates with parameters of left ventricular hypertrophy in patients with hypertrophic cardiomyopathy.
Orosz A; Baczkó I; Nagy V; Gavallér H; Csanády M; Forster T; Papp JG; Varró A; Lengyel C; Sepp R
Can J Physiol Pharmacol; 2015 Sep; 93(9):765-72. PubMed ID: 26313025
[TBL] [Abstract][Full Text] [Related]
9. Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window current.
Landstrom AP; Boczek NJ; Ye D; Miyake CY; De la Uz CM; Allen HD; Ackerman MJ; Kim JJ
Int J Cardiol; 2016 Oct; 220():290-8. PubMed ID: 27390944
[TBL] [Abstract][Full Text] [Related]
10. [P1208fs mutation in the cardiac myosin binding protein C is associated with hypertrophic cardiomyopathy in a Chinese pedigree].
Li J; Liu LW; Na LS; Zuo L; Qi W; Liu Y; Shao H; Ma ZL; Wang LF
Zhonghua Xin Xue Guan Bing Za Zhi; 2016 Apr; 44(4):321-6. PubMed ID: 27112610
[TBL] [Abstract][Full Text] [Related]
11. Gene mutations in apical hypertrophic cardiomyopathy.
Arad M; Penas-Lado M; Monserrat L; Maron BJ; Sherrid M; Ho CY; Barr S; Karim A; Olson TM; Kamisago M; Seidman JG; Seidman CE
Circulation; 2005 Nov; 112(18):2805-11. PubMed ID: 16267253
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Burashnikov E; Pfeiffer R; Barajas-Martinez H; Delpón E; Hu D; Desai M; Borggrefe M; Häissaguerre M; Kanter R; Pollevick GD; Guerchicoff A; Laiño R; Marieb M; Nademanee K; Nam GB; Robles R; Schimpf R; Stapleton DD; Viskin S; Winters S; Wolpert C; Zimmern S; Veltmann C; Antzelevitch C
Heart Rhythm; 2010 Dec; 7(12):1872-82. PubMed ID: 20817017
[TBL] [Abstract][Full Text] [Related]
13. Temporal repolarization lability in hypertrophic cardiomyopathy caused by beta-myosin heavy-chain gene mutations.
Atiga WL; Fananapazir L; McAreavey D; Calkins H; Berger RD
Circulation; 2000 Mar; 101(11):1237-42. PubMed ID: 10725281
[TBL] [Abstract][Full Text] [Related]
14. Ultrasonic Assessment of Myocardial Microstructure in Hypertrophic Cardiomyopathy Sarcomere Mutation Carriers With and Without Left Ventricular Hypertrophy.
Hiremath P; Lawler PR; Ho JE; Correia AW; Abbasi SA; Kwong RY; Jerosch-Herold M; Ho CY; Cheng S
Circ Heart Fail; 2016 Sep; 9(9):. PubMed ID: 27623770
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Purevjav E; Arimura T; Augustin S; Huby AC; Takagi K; Nunoda S; Kearney DL; Taylor MD; Terasaki F; Bos JM; Ommen SR; Shibata H; Takahashi M; Itoh-Satoh M; McKenna WJ; Murphy RT; Labeit S; Yamanaka Y; Machida N; Park JE; Alexander PM; Weintraub RG; Kitaura Y; Ackerman MJ; Kimura A; Towbin JA
Hum Mol Genet; 2012 May; 21(9):2039-53. PubMed ID: 22286171
[TBL] [Abstract][Full Text] [Related]
17. Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations.
Zhu YB; Luo JW; Jiang F; Liu G
Mol Med Rep; 2018 May; 17(5):7073-7080. PubMed ID: 29568937
[TBL] [Abstract][Full Text] [Related]
18. Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives.
Andersen PS; Havndrup O; Hougs L; Sørensen KM; Jensen M; Larsen LA; Hedley P; Thomsen AR; Moolman-Smook J; Christiansen M; Bundgaard H
Hum Mutat; 2009 Mar; 30(3):363-70. PubMed ID: 19035361
[TBL] [Abstract][Full Text] [Related]
19. CSRP3, p.Arg122*, is responsible for hypertrophic cardiomyopathy in a Chinese family.
Huang H; Chen Y; Jin J; Du R; Tang K; Fan L; Xiang R
J Gene Med; 2022 Jan; 24(1):e3390. PubMed ID: 34558151
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6).
Templin C; Ghadri JR; Rougier JS; Baumer A; Kaplan V; Albesa M; Sticht H; Rauch A; Puleo C; Hu D; Barajas-Martinez H; Antzelevitch C; Lüscher TF; Abriel H; Duru F
Eur Heart J; 2011 May; 32(9):1077-88. PubMed ID: 21383000
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
