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Rare Variation in Drug Metabolism and Long QT Genes and the Genetic Susceptibility to Acquired Long QT Syndrome.
Gray B, Baruteau AE, Antolin AA, Pittman A, Sarganas G, Molokhia M, Blom MT, Bastiaenen R, Bardai A, Priori SG, Napolitano C, Weeke PE, Shakir SA, Haverkamp W, Mestres J, Winkel BG, Witney AA, Chis-Ster I, Sangaralingam A, Camm AJ, Tfelt-Hansen J, Roden DM, Tan HL, Garbe E, Sturkenboom M, Behr ER. Gray B, et al. Among authors: priori sg. Circ Genom Precis Med. 2022 Feb;15(1):e003391. doi: 10.1161/CIRCGEN.121.003391. Epub 2022 Feb 3. Circ Genom Precis Med. 2022. PMID: 35113648
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.
Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS, Colatsky TJ. Schwartz PJ, et al. Among authors: priori sg. Circulation. 1995 Dec 15;92(12):3381-6. doi: 10.1161/01.cir.92.12.3381. Circulation. 1995. PMID: 8521555
Molecular biology of the long QT syndrome: impact on management.
Priori SG, Napolitano C, Paganini V, Cantù F, Schwartz PJ. Priori SG, et al. Pacing Clin Electrophysiol. 1997 Aug;20(8 Pt 2):2052-7. doi: 10.1111/j.1540-8159.1997.tb03626.x. Pacing Clin Electrophysiol. 1997. PMID: 9272507 Review.
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
Li H, Chen Q, Moss AJ, Robinson J, Goytia V, Perry JC, Vincent GM, Priori SG, Lehmann MH, Denfield SW, Duff D, Kaine S, Shimizu W, Schwartz PJ, Wang Q, Towbin JA. Li H, et al. Among authors: priori sg. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196
446 results