Iturralde-Torres, Pedro

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Number of items: 8.

Journal Article

González-Melchor, Laila; Villarreal-Molina, Teresa; Iturralde-Torres, Pedro; Medeiros Domingo, Argelia (2014). Sudden cardiac death in individuals with normal hearts: an update. Archivos de cardiología de México, 84(4), pp. 293-304. Elsevier España 10.1016/j.acmx.2014.04.002

Iturralde-Torres, Pedro; Medeiros Domingo, Argelia (2009). Genetic in long QT syndromes. Archivos de cardiología de México, 79 Suppl 2, pp. 26-30. Instituto Nacional de Cardiología Ignacio Chávez

Medeiros Domingo, Argelia; Tan, Bi-Hua; Iturralde-Torres, Pedro; Tester, David J.; Tusié-Luna, Teresa; Makielski, Jonathan C.; Ackerman, Michael J. (2009). Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A. Heart rhythm, 6(8), pp. 1170-1175. Elsevier 10.1016/j.hrthm.2009.04.034

Iturralde-Torres, Pedro; Nava-Townsend, Santiago; Gómez-Flores, Jorge; Medeiros Domingo, Argelia; Colín-Lizalde, Luis; Hermosillo, Antonio G.; Victoria, Diana; Márquez, Manlio F. (2008). Association of congenital, diffuse electrical disease in children with normal heart: sick sinus syndrome, intraventricular conduction block, and monomorphic ventricular tachycardia. Journal of cardiovascular electrophysiology, 19(5), pp. 550-555. Wiley-Blackwell 10.1111/j.1540-8167.2007.01006.x

Tan, Bi-Hua; Iturralde-Torres, Pedro; Medeiros Domingo, Argelia; Nava, Santiago; Tester, David J.; Valdivia, Carmen R.; Tusié-Luna, Teresa; Ackerman, Michael J.; Makielski, Jonathan C. (2007). A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Cardiovascular research, 76(3), pp. 409-417. Oxford University Press 10.1016/j.cardiores.2007.08.006

Medeiros Domingo, Argelia; Kaku, Toshihiko; Tester, David J; Iturralde-Torres, Pedro; Itty, Ajit; Ye, Bin; Valdivia, Carmen; Ueda, Kazuo; Canizales-Quinteros, Samuel; Tusié-Luna, Maria Teresa; Makielski, Jonathan C.; Ackerman, Michael J. (2007). SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome. Circulation, 116(2), pp. 134-142. Lippincott Williams & Wilkins 10.1161/CIRCULATIONAHA.106.659086

Medeiros Domingo, Argelia; Iturralde-Torres, Pedro; Ackerman, Michael J. (2007). Clinical and genetic characteristics of long QT syndrome. Revista española de cardiología, 60(7), pp. 739-752. Elsevier

Medeiros Domingo, Argelia; Iturralde-Torres, Pedro; Canizales-Quinteros, Samuel; Hernández-Cruz, Arturo; Tusié-Luna, M. Teresa (2007). New perspectives in long QT syndrome. Revista de investigación clínica; organo del Hospital de Enfermedades de la Nutrición, 59(1), pp. 57-72. Instituto Nacional de la Nutricion "Salvador Zubiran"

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