Priori SG - Search Results

1

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

Splawski I, Timothy KW, Sharpe LM, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz PJ, Joseph RM, Condouris K, Tager-Flusberg H, Priori SG, Sanguinetti MC, Keating MT. Splawski I, et al. Among authors: priori sg. Cell. 2004 Oct 1;119(1):19-31. doi: 10.1016/j.cell.2004.09.011. Cell. 2004. PMID: 15454078 Free article.

2

A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.

Mohler PJ, Splawski I, Napolitano C, Bottelli G, Sharpe L, Timothy K, Priori SG, Keating MT, Bennett V. Mohler PJ, et al. Among authors: priori sg. Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):9137-42. doi: 10.1073/pnas.0402546101. Epub 2004 Jun 3. Proc Natl Acad Sci U S A. 2004. PMID: 15178757 Free PMC article.

3

Gene-specific therapy for inherited arrhythmogenic diseases.

Napolitano C, Bloise R, Priori SG. Napolitano C, et al. Among authors: priori sg. Pharmacol Ther. 2006 Apr;110(1):1-13. doi: 10.1016/j.pharmthera.2005.08.003. Epub 2005 Sep 15. Pharmacol Ther. 2006. PMID: 16168489 Review.

4

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Splawski I, et al. Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178. Circulation. 2000. PMID: 10973849

5

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

Wang Q, Shen J, Li Z, Timothy K, Vincent GM, Priori SG, Schwartz PJ, Keating MT. Wang Q, et al. Among authors: priori sg. Hum Mol Genet. 1995 Sep;4(9):1603-7. doi: 10.1093/hmg/4.9.1603. Hum Mol Genet. 1995. PMID: 8541846

6

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.

7

Inherited arrhythmia syndromes: applying the molecular biology and genetic to the clinical management.

Priori SG, Napolitano C, Vicentini A. Priori SG, et al. J Interv Card Electrophysiol. 2003 Oct;9(2):93-101. doi: 10.1023/a:1026255617913. J Interv Card Electrophysiol. 2003. PMID: 14574020 Review.

8

Should patients with an asymptomatic Brugada electrocardiogram undergo pharmacological and electrophysiological testing?

Priori SG, Napolitano C. Priori SG, et al. Circulation. 2005 Jul 12;112(2):279-92; discussion 279-92. Circulation. 2005. PMID: 16013094 No abstract available.

9

Cardiac and skeletal muscle disorders caused by mutations in the intracellular Ca2+ release channels.

Priori SG, Napolitano C. Priori SG, et al. J Clin Invest. 2005 Aug;115(8):2033-8. doi: 10.1172/JCI25664. J Clin Invest. 2005. PMID: 16075044 Free PMC article. Review.

10

Role of genetic analyses in cardiology: part I: mendelian diseases: cardiac channelopathies.

Priori SG, Napolitano C. Priori SG, et al. Circulation. 2006 Feb 28;113(8):1130-5. doi: 10.1161/CIRCULATIONAHA.105.563205. Circulation. 2006. PMID: 16505190 Review.

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