Priori S - Search Results

1

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.

Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ. Marks AR, et al. Among authors: priori s. J Cell Physiol. 2002 Jan;190(1):1-6. doi: 10.1002/jcp.10031. J Cell Physiol. 2002. PMID: 11807805 Review.

2

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death.

Wehrens XH, Lehnart SE, Huang F, Vest JA, Reiken SR, Mohler PJ, Sun J, Guatimosim S, Song LS, Rosemblit N, D'Armiento JM, Napolitano C, Memmi M, Priori SG, Lederer WJ, Marks AR. Wehrens XH, et al. Among authors: priori sg. Cell. 2003 Jun 27;113(7):829-40. doi: 10.1016/s0092-8674(03)00434-3. Cell. 2003. PMID: 12837242 Free article.

3

Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT).

Napolitano C, Bloise R, Memmi M, Priori SG. Napolitano C, et al. Eur J Hum Genet. 2014 Jan;22(1). doi: 10.1038/ejhg.2013.55. Epub 2013 Apr 3. Eur J Hum Genet. 2014. PMID: 23549275 Free PMC article. No abstract available.

4

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, DeSimone L, Coltorti F, Bloise R, Keegan R, Cruz Filho FE, Vignati G, Benatar A, DeLogu A. Priori SG, et al. Circulation. 2002 Jul 2;106(1):69-74. doi: 10.1161/01.cir.0000020013.73106.d8. Circulation. 2002. PMID: 12093772

5

Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model.

Liu N, Colombi B, Memmi M, Zissimopoulos S, Rizzi N, Negri S, Imbriani M, Napolitano C, Lai FA, Priori SG. Liu N, et al. Among authors: priori sg. Circ Res. 2006 Aug 4;99(3):292-8. doi: 10.1161/01.RES.0000235869.50747.e1. Epub 2006 Jul 6. Circ Res. 2006. PMID: 16825580

6

Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia.

di Barletta MR, Viatchenko-Karpinski S, Nori A, Memmi M, Terentyev D, Turcato F, Valle G, Rizzi N, Napolitano C, Gyorke S, Volpe P, Priori SG. di Barletta MR, et al. Among authors: priori sg. Circulation. 2006 Sep 5;114(10):1012-9. doi: 10.1161/CIRCULATIONAHA.106.623793. Epub 2006 Aug 14. Circulation. 2006. PMID: 16908766

7

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers.

Mazzanti A, Kukavica D, Trancuccio A, Memmi M, Bloise R, Gambelli P, Marino M, Ortíz-Genga M, Morini M, Monteforte N, Giordano U, Keegan R, Tomasi L, Anastasakis A, Davis AM, Shimizu W, Blom NA, Santiago DJ, Napolitano C, Monserrat L, Priori SG. Mazzanti A, et al. JAMA Cardiol. 2022 May 1;7(5):504-512. doi: 10.1001/jamacardio.2022.0219. JAMA Cardiol. 2022. PMID: 35353122 Free PMC article.

8

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, Sorrentino V, Danieli GA. Priori SG, et al. Circulation. 2001 Jan 16;103(2):196-200. doi: 10.1161/01.cir.103.2.196. Circulation. 2001. PMID: 11208676

9

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation.

Grant AO, Carboni MP, Neplioueva V, Starmer CF, Memmi M, Napolitano C, Priori S. Grant AO, et al. Among authors: priori s. J Clin Invest. 2002 Oct;110(8):1201-9. doi: 10.1172/JCI15570. J Clin Invest. 2002. PMID: 12393856 Free PMC article.

10

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.

Rivolta I, Abriel H, Tateyama M, Liu H, Memmi M, Vardas P, Napolitano C, Priori SG, Kass RS. Rivolta I, et al. Among authors: priori sg. J Biol Chem. 2001 Aug 17;276(33):30623-30. doi: 10.1074/jbc.M104471200. Epub 2001 Jun 15. J Biol Chem. 2001. PMID: 11410597 Free article.

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