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Results: 1 to 20 of 91

1.

Brugada syndrome in spinal and bulbar muscular atrophy.

Araki A, Katsuno M, Suzuki K, Banno H, Suga N, Hashizume A, Mano T, Hijikata Y, Nakatsuji H, Watanabe H, Yamamoto M, Makiyama T, Ohno S, Fukuyama M, Morimoto S, Horie M, Sobue G.

Neurology. 2014 May 20;82(20):1813-21. doi: 10.1212/WNL.0000000000000434. Epub 2014 Apr 23.

PMID:
24759840
[PubMed - indexed for MEDLINE]
2.

The role of late I Na in development of cardiac arrhythmias.

Antzelevitch C, Nesterenko V, Shryock JC, Rajamani S, Song Y, Belardinelli L.

Handb Exp Pharmacol. 2014;221:137-68. doi: 10.1007/978-3-642-41588-3_7. Review.

PMID:
24737235
[PubMed - indexed for MEDLINE]
3.

A common genetic variant within SCN10A modulates cardiac SCN5A expression.

van den Boogaard M, Smemo S, Burnicka-Turek O, Arnolds DE, van de Werken HJ, Klous P, McKean D, Muehlschlegel JD, Moosmann J, Toka O, Yang XH, Koopmann TT, Adriaens ME, Bezzina CR, de Laat W, Seidman C, Seidman JG, Christoffels VM, Nobrega MA, Barnett P, Moskowitz IP.

J Clin Invest. 2014 Apr 1;124(4):1844-52. doi: 10.1172/JCI73140. Epub 2014 Mar 18.

PMID:
24642470
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Nav-igating through a complex landscape: SCN10A and cardiac conduction.

Park DS, Fishman GI.

J Clin Invest. 2014 Apr 1;124(4):1460-2. doi: 10.1172/JCI75240. Epub 2014 Mar 18.

PMID:
24642462
[PubMed - indexed for MEDLINE]
5.

Loss-of-function of the voltage-gated sodium channel NaV1.5 (channelopathies) in patients with irritable bowel syndrome.

Beyder A, Mazzone A, Strege PR, Tester DJ, Saito YA, Bernard CE, Enders FT, Ek WE, Schmidt PT, Dlugosz A, Lindberg G, Karling P, Ohlsson B, Gazouli M, Nardone G, Cuomo R, Usai-Satta P, Galeazzi F, Neri M, Portincasa P, Bellini M, Barbara G, Camilleri M, Locke GR 3rd, Talley NJ, D'Amato M, Ackerman MJ, Farrugia G.

Gastroenterology. 2014 Jun;146(7):1659-68. doi: 10.1053/j.gastro.2014.02.054. Epub 2014 Mar 5.

PMID:
24613995
[PubMed - indexed for MEDLINE]
6.

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.

Christiansen M, Hedley PL, Theilade J, Stoevring B, Leren TP, Eschen O, Sørensen KM, Tybjærg-Hansen A, Ousager LB, Pedersen LN, Frikke-Schmidt R, Aidt FH, Hansen MG, Hansen J, Bloch Thomsen PE, Toft E, Henriksen FL, Bundgaard H, Jensen HK, Kanters JK.

BMC Med Genet. 2014 Mar 7;15:31. doi: 10.1186/1471-2350-15-31.

PMID:
24606995
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic variants for long QT syndrome among infants and children from a statewide newborn hearing screening program cohort.

Chang RK, Lan YT, Silka MJ, Morrow H, Kwong A, Smith-Lang J, Wallerstein R, Lin HJ.

J Pediatr. 2014 Mar;164(3):590-5.e1-3. doi: 10.1016/j.jpeds.2013.11.011. Epub 2013 Dec 31.

PMID:
24388587
[PubMed - indexed for MEDLINE]
8.

Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: the Jackson Heart Study.

Akylbekova EL, Payne JP, Newton-Cheh C, May WL, Fox ER, Wilson JG, Sarpong DF, Taylor HA, Maher JF.

Am Heart J. 2014 Jan;167(1):116-122.e1. doi: 10.1016/j.ahj.2013.10.009. Epub 2013 Oct 22.

PMID:
24332150
[PubMed - indexed for MEDLINE]
9.

A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese?

Shen C, Xu L, Yang Z, Zou Y, Hu K, Fan Z, Ge J, Sun A.

Dis Markers. 2013;35(5):531-5. doi: 10.1155/2013/659528. Epub 2013 Oct 20.

PMID:
24227891
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Long QT syndrome in South Africa: the results of comprehensive genetic screening.

Hedley PL, Durrheim GA, Hendricks F, Goosen A, Jespersgaard C, Støvring B, Pham TT, Christiansen M, Brink PA, Corfield VA.

Cardiovasc J Afr. 2013 Jul;24(6):231-7. doi: 10.5830/CVJA-2013-032.

PMID:
24217263
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Update of diagnosis and management of inherited cardiac arrhythmias.

Shimizu W.

Circ J. 2013;77(12):2867-72. Epub 2013 Nov 7. Review.

PMID:
24200848
[PubMed - indexed for MEDLINE]
Free Article
12.

Electrophysiological characteristics of a SCN5A voltage sensors mutation R1629Q associated with Brugada syndrome.

Zeng Z, Zhou J, Hou Y, Liang X, Zhang Z, Xu X, Xie Q, Li W, Huang Z.

PLoS One. 2013 Oct 22;8(10):e78382. doi: 10.1371/journal.pone.0078382. eCollection 2013.

PMID:
24167619
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Long QT syndrome: a Korean single center study.

Lee YS, Kwon BS, Kim GB, Oh SI, Bae EJ, Park SS, Noh CI.

J Korean Med Sci. 2013 Oct;28(10):1454-60. doi: 10.3346/jkms.2013.28.10.1454. Epub 2013 Sep 25.

PMID:
24133349
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Electrical stimulation promotes maturation of cardiomyocytes derived from human embryonic stem cells.

Chan YC, Ting S, Lee YK, Ng KM, Zhang J, Chen Z, Siu CW, Oh SK, Tse HF.

J Cardiovasc Transl Res. 2013 Dec;6(6):989-99. doi: 10.1007/s12265-013-9510-z. Epub 2013 Oct 1.

PMID:
24081385
[PubMed - indexed for MEDLINE]
15.

Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease.

Fedele F, Mancone M, Chilian WM, Severino P, Canali E, Logan S, De Marchis ML, Volterrani M, Palmirotta R, Guadagni F.

Basic Res Cardiol. 2013;108(6):387. doi: 10.1007/s00395-013-0387-4. Epub 2013 Sep 26.

PMID:
24068186
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Unfolded protein response regulates cardiac sodium current in systolic human heart failure.

Gao G, Xie A, Zhang J, Herman AM, Jeong EM, Gu L, Liu M, Yang KC, Kamp TJ, Dudley SC.

Circ Arrhythm Electrophysiol. 2013 Oct;6(5):1018-24. doi: 10.1161/CIRCEP.113.000274. Epub 2013 Sep 13.

PMID:
24036084
[PubMed - indexed for MEDLINE]
17.

Modeling type 3 long QT syndrome with cardiomyocytes derived from patient-specific induced pluripotent stem cells.

Ma D, Wei H, Zhao Y, Lu J, Li G, Sahib NB, Tan TH, Wong KY, Shim W, Wong P, Cook SA, Liew R.

Int J Cardiol. 2013 Oct 15;168(6):5277-86. doi: 10.1016/j.ijcard.2013.08.015. Epub 2013 Aug 15.

PMID:
23998552
[PubMed - indexed for MEDLINE]
18.

Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.

Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW.

Circ Arrhythm Electrophysiol. 2013 Oct;6(5):946-51. doi: 10.1161/CIRCEP.113.000618. Epub 2013 Aug 30.

PMID:
23995044
[PubMed - indexed for MEDLINE]
19.

A novel deletion-frameshift mutation in the S1 region of HERG gene in a Chinese family with long QT syndrome.

Gao Y, Zhang P, Li XB, Wu CC, Guo JH.

Chin Med J (Engl). 2013 Aug;126(16):3093-6.

PMID:
23981618
[PubMed - indexed for MEDLINE]
Free Article
20.

A novel SCN5A mutation demonstrating a variety of clinical phenotypes in familial sick sinus syndrome.

Nakajima S, Makiyama T, Hanazawa K, Kaitani K, Amano M, Hayama Y, Onishi N, Tamaki Y, Miyake M, Tamura T, Kondo H, Motooka M, Izumi C, Nakagawa Y, Horie M.

Intern Med. 2013;52(16):1805-8. Epub 2012 Mar 1.

PMID:
23955615
[PubMed - indexed for MEDLINE]
Free Article

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