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Items: 1 to 20 of 307

1.

Genetic modulators of the phenotype in the long QT syndrome: state of the art and clinical impact.

Napolitano C, Novelli V, Francis MD, Priori SG.

Curr Opin Genet Dev. 2015 Aug 1;33:17-24. doi: 10.1016/j.gde.2015.06.009. [Epub ahead of print] Review.

PMID:
26241467
2.

Genetics of sudden cardiac death.

Bezzina CR, Lahrouchi N, Priori SG.

Circ Res. 2015 Jun 5;116(12):1919-36. doi: 10.1161/CIRCRESAHA.116.304030. Review.

PMID:
26044248
3.

Use of whole exome sequencing for the identification of Ito-based arrhythmia mechanism and therapy.

Sturm AC, Kline CF, Glynn P, Johnson BL, Curran J, Kilic A, Higgins RS, Binkley PF, Janssen PM, Weiss R, Raman SV, Fowler SJ, Priori SG, Hund TJ, Carnes CA, Mohler PJ.

J Am Heart Assoc. 2015 May 26;4(5). pii: e001762. doi: 10.1161/JAHA.114.001762.

4.

Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome.

Harrell DT, Ashihara T, Ishikawa T, Tominaga I, Mazzanti A, Takahashi K, Oginosawa Y, Abe H, Maemura K, Sumitomo N, Uno K, Takano M, Priori SG, Makita N.

Int J Cardiol. 2015 Jul 1;190:393-402. doi: 10.1016/j.ijcard.2015.04.090. Epub 2015 Apr 15.

PMID:
25974115
5.

Gene therapy to treat cardiac arrhythmias.

Bongianino R, Priori SG.

Nat Rev Cardiol. 2015 Sep;12(9):531-46. doi: 10.1038/nrcardio.2015.61. Epub 2015 Apr 28. Review.

PMID:
25917154
6.

hERG Blockade by Iboga Alkaloids.

Alper K, Bai R, Liu N, Fowler SJ, Huang XP, Priori SG, Ruan Y.

Cardiovasc Toxicol. 2015 Jan 31. [Epub ahead of print]

PMID:
25636206
7.

Neuronal Na+ channel blockade suppresses arrhythmogenic diastolic Ca2+ release.

Radwański PB, Brunello L, Veeraraghavan R, Ho HT, Lou Q, Makara MA, Belevych AE, Anghelescu M, Priori SG, Volpe P, Hund TJ, Janssen PM, Mohler PJ, Bridge JH, Poelzing S, Györke S.

Cardiovasc Res. 2015 Apr 1;106(1):143-52. doi: 10.1093/cvr/cvu262. Epub 2014 Dec 23.

PMID:
25538156
8.

[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
9.

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.

10.

From decision to shared-decision: Introducing patients' preferences into clinical decision analysis.

Sacchi L, Rubrichi S, Rognoni C, Panzarasa S, Parimbelli E, Mazzanti A, Napolitano C, Priori SG, Quaglini S.

Artif Intell Med. 2014 Nov 1. pii: S0933-3657(14)00107-9. doi: 10.1016/j.artmed.2014.10.004. [Epub ahead of print]

PMID:
25455562
11.

Rationale and design of the Pan-African Sudden Cardiac Death survey: the Pan-African SCD study.

Bonny A, Ngantcha M, Amougou SN, Kane A, Marrakchi S, Okello E, Taty G, Gehani A, Diakite M, Talle M, Lambiase P, Houenassi M, Chin A, Otieno H, Temu G, Owusu IK, Karaye KM, Awad AA, Winkel BG, Priori SG; Pan‐African Society of Cardiology (PASCAR) Task Force on Sudden Cardiac Death.

Cardiovasc J Afr. 2014 Jul-Aug;25(4):176-84. doi: 10.5830/CVJA-2014-035.

12.

Epidemiology of sudden cardiac death in Cameroon: rationale and design of the Douala-SUD survey.

Bonny A, Noah DN, Ngantcha M, Ateh R, Saka C, Wa J, Fonga R, Amougou SN, Gregers Winkel B, Lambiase P, Priori SG; Douala Sudden Unexplained Death (Douala-SUD) study group.

Arch Cardiovasc Dis. 2014 Aug-Sep;107(8-9):433-42. doi: 10.1016/j.acvd.2014.05.005. Epub 2014 Jul 19.

PMID:
25047994
13.

Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced age.

Denegri M, Bongianino R, Lodola F, Boncompagni S, De Giusti VC, Avelino-Cruz JE, Liu N, Persampieri S, Curcio A, Esposito F, Pietrangelo L, Marty I, Villani L, Moyaho A, Baiardi P, Auricchio A, Protasi F, Napolitano C, Priori SG.

Circulation. 2014 Jun 24;129(25):2673-81. doi: 10.1161/CIRCULATIONAHA.113.006901. Epub 2014 Jun 2.

14.

The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases.

Mazzanti A, O'Rourke S, Ng K, Miceli C, Borio G, Curcio A, Esposito F, Napolitano C, Priori SG.

Expert Rev Cardiovasc Ther. 2014 Apr;12(4):499-519. doi: 10.1586/14779072.2014.894884. Review.

PMID:
24650315
15.

Genetic testing to predict sudden cardiac death: current perspectives and future goals.

Priori SG.

Indian Heart J. 2014 Jan-Feb;66 Suppl 1:S58-60. doi: 10.1016/j.ihj.2013.11.004. Epub 2013 Dec 22. Review.

16.

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.

Cerrone M, Lin X, Zhang M, Agullo-Pascual E, Pfenniger A, Chkourko Gusky H, Novelli V, Kim C, Tirasawadichai T, Judge DP, Rothenberg E, Chen HS, Napolitano C, Priori SG, Delmar M.

Circulation. 2014 Mar 11;129(10):1092-103. doi: 10.1161/CIRCULATIONAHA.113.003077. Epub 2013 Dec 18.

17.

Subclinical abnormalities in sarcoplasmic reticulum Ca(2+) release promote eccentric myocardial remodeling and pump failure death in response to pressure overload.

Sedej S, Schmidt A, Denegri M, Walther S, Matovina M, Arnstein G, Gutschi EM, Windhager I, Ljubojević S, Negri S, Heinzel FR, Bisping E, Vos MA, Napolitano C, Priori SG, Kockskämper J, Pieske B.

J Am Coll Cardiol. 2014 Apr 22;63(15):1569-79. doi: 10.1016/j.jacc.2013.11.010. Epub 2013 Dec 4.

18.

Clinical and research data integration: the i2b2-FSM experience.

Segagni D, Tibollo V, Dagliati A, Malovini A, Zambelli A, Napolitano C, Priori SG, Bellazzi R.

AMIA Jt Summits Transl Sci Proc. 2013 Mar 18;2013:239-40. eCollection 2013.

PMID:
24303274
19.

Novel insight into the natural history of short QT syndrome.

Mazzanti A, Kanthan A, Monteforte N, Memmi M, Bloise R, Novelli V, Miceli C, O'Rourke S, Borio G, Zienciuk-Krajka A, Curcio A, Surducan AE, Colombo M, Napolitano C, Priori SG.

J Am Coll Cardiol. 2014 Apr 8;63(13):1300-8. doi: 10.1016/j.jacc.2013.09.078. Epub 2013 Nov 28.

20.

CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia.

Di Pasquale E, Lodola F, Miragoli M, Denegri M, Avelino-Cruz JE, Buonocore M, Nakahama H, Portararo P, Bloise R, Napolitano C, Condorelli G, Priori SG.

Cell Death Dis. 2013 Oct 10;4:e843. doi: 10.1038/cddis.2013.369.

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