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Results: 1 to 20 of 500

PubMed for MedGen (Select 468523)

1.

Diagnosis of Brugada syndrome during fever: a case report from a tertiary care centre.

Boda S, Mishra PC, Naik BS.

J Assoc Physicians India. 2014 Jul;62(7):616-9.

PMID:
25672038
2.

[Clinical polymorphisms and approaches of arrhythmias treatment in a family with δKPQ1505-1507 deletion in SCN5A gene].

Saber S, Houshmand M, Eftekhharzadeh M, Samiei N, Fazelifar AF, Haghjoo M, Zakliaz'minskaia EV, Gavrilenko AV.

Vestn Ross Akad Med Nauk. 2014;(5-6):52-9. Russian.

PMID:
25558681
3.

[Role of standard resting ECG in the assessment of sudden cardiac death risk].

Napolitano C, Priori SG.

G Ital Cardiol (Rome). 2014 Dec;15(12):670-7. doi: 10.1714/1718.18768. Review. Italian.

PMID:
25533116
4.

Genetically engineered SCN5A mutant pig hearts exhibit conduction defects and arrhythmias.

Park DS, Cerrone M, Morley G, Vasquez C, Fowler S, Liu N, Bernstein SA, Liu FY, Zhang J, Rogers CS, Priori SG, Chinitz LA, Fishman GI.

J Clin Invest. 2015 Jan;125(1):403-12. doi: 10.1172/JCI76919. Epub 2014 Dec 15.

5.

Bringing home the bacon? The next step in cardiac sodium channelopathies.

Wilde AA, Postema PG.

J Clin Invest. 2015 Jan;125(1):99-101. doi: 10.1172/JCI80014. Epub 2014 Dec 15.

PMID:
25500878
6.

Transcranial magnetic stimulation as an antidepressant alternative in a patient with Brugada syndrome and recurrent syncope.

Alampay MM, Haigney MC, Flanagan MC, Perito RM, Love KM, Grammer GG.

Mayo Clin Proc. 2014 Nov;89(11):1584-7. doi: 10.1016/j.mayocp.2014.08.010. Epub 2014 Nov 3.

PMID:
25444490
7.

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.

Béziau DM, Barc J, O'Hara T, Le Gloan L, Amarouch MY, Solnon A, Pavin D, Lecointe S, Bouillet P, Gourraud JB, Guicheney P, Denjoy I, Redon R, Mabo P, le Marec H, Loussouarn G, Kyndt F, Schott JJ, Probst V, Baró I.

Basic Res Cardiol. 2014;109(6):446. doi: 10.1007/s00395-014-0446-5. Epub 2014 Oct 24.

PMID:
25341504
8.

Hey bHLH transcription factors.

Weber D, Wiese C, Gessler M.

Curr Top Dev Biol. 2014;110:285-315. doi: 10.1016/B978-0-12-405943-6.00008-7. Review.

PMID:
25248480
9.

Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience.

Wong LC, Roses-Noguer F, Till JA, Behr ER.

Circ Arrhythm Electrophysiol. 2014 Oct;7(5):800-6. doi: 10.1161/CIRCEP.114.001818. Epub 2014 Sep 6.

PMID:
25194972
10.

Clinical and genetic diagnosis for inherited cardiac arrhythmias.

Shimizu W.

J Nippon Med Sch. 2014;81(4):203-10. Review.

11.

[Genetic arrhythmias and gender].

Biernacka EK.

Przegl Lek. 2014;71(3):139-41. Review. Polish.

PMID:
25154209
12.

SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction.

Boehringer T, Bugert P, Borggrefe M, Elmas E.

Mol Med Rep. 2014 Oct;10(4):2039-44. doi: 10.3892/mmr.2014.2401. Epub 2014 Jul 21.

PMID:
25051102
13.

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome.

Hu D, Barajas-Martínez H, Pfeiffer R, Dezi F, Pfeiffer J, Buch T, Betzenhauser MJ, Belardinelli L, Kahlig KM, Rajamani S, DeAntonio HJ, Myerburg RJ, Ito H, Deshmukh P, Marieb M, Nam GB, Bhatia A, Hasdemir C, Haïssaguerre M, Veltmann C, Schimpf R, Borggrefe M, Viskin S, Antzelevitch C.

J Am Coll Cardiol. 2014 Jul 8;64(1):66-79. doi: 10.1016/j.jacc.2014.04.032.

PMID:
24998131
14.

Cardiac sodium channels and inherited electrophysiological disorders: an update on the pharmacotherapy.

van Hoeijen DA, Blom MT, Tan HL.

Expert Opin Pharmacother. 2014 Sep;15(13):1875-87. doi: 10.1517/14656566.2014.936380. Epub 2014 Jul 3. Review.

PMID:
24992280
15.

Characterization of SEMA3A-encoded semaphorin as a naturally occurring Kv4.3 protein inhibitor and its contribution to Brugada syndrome.

Boczek NJ, Ye D, Johnson EK, Wang W, Crotti L, Tester DJ, Dagradi F, Mizusawa Y, Torchio M, Alders M, Giudicessi JR, Wilde AA, Schwartz PJ, Nerbonne JM, Ackerman MJ.

Circ Res. 2014 Aug 1;115(4):460-9. doi: 10.1161/CIRCRESAHA.115.303657. Epub 2014 Jun 24.

PMID:
24963029
16.

Brugada syndrome.

Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada P.

Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):25-8. Review.

17.

Sudden cardiac death from parvovirus B19 myocarditis in a young man with Brugada syndrome.

Juhasz Z, Tiszlavicz L, Kele B, Terhes G, Deak J, Rudas L, Kereszty E.

J Forensic Leg Med. 2014 Jul;25:8-13. doi: 10.1016/j.jflm.2014.04.018. Epub 2014 Apr 29.

PMID:
24931854
18.

Sodium channels, cardiac arrhythmia, and therapeutic strategy.

Miller D, Wang L, Zhong J.

Adv Pharmacol. 2014;70:367-92. doi: 10.1016/B978-0-12-417197-8.00012-2. Review.

PMID:
24931202
19.

Arrhythmic substrate, slowed propagation and increased dispersion in conduction direction in the right ventricular outflow tract of murine Scn5a+/- hearts.

Zhang Y, Guzadhur L, Jeevaratnam K, Salvage SC, Matthews GD, Lammers WJ, Lei M, Huang CL, Fraser JA.

Acta Physiol (Oxf). 2014 Aug;211(4):559-73. doi: 10.1111/apha.12324. Epub 2014 Jul 9.

20.

Risk stratification and treatment of brugada syndrome.

Arbelo E, Brugada J.

Curr Cardiol Rep. 2014 Jul;16(7):508. doi: 10.1007/s11886-014-0508-1. Review.

PMID:
24893941
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