Fabiana Scornik, PhD
Affiliations: | Masonic Medical Research Laboratory, Utica, Frankfort, NY, United States |
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"Fabiana Scornik"Mean distance: 17.21 (cluster 32) | S | N | B | C | P |
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Publications
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| Martinez-Moreno R, Selga E, Riuró H, et al. (2020) An Variant Affects Both Cardiac-Type (Na1.5) and Brain-Type (Na1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders. Frontiers in Cell and Developmental Biology. 8: 528742 |
| Yeste M, Llavanera M, Pérez G, et al. (2019) Elucidating the Role of K Channels during In Vitro Capacitation of Boar Spermatozoa: Do SLO1 Channels Play a Crucial Role? International Journal of Molecular Sciences. 20 |
| Santori M, Gil R, Blanco-Verea A, et al. (2019) Sudden infant death as the most severe phenotype caused by genetic modulation in a family with atrial fibrillation. Forensic Science International. Genetics. 43: 102159 |
| Cuyàs E, Gumuzio J, Lozano-Sánchez J, et al. (2019) Extra Virgin Olive Oil Contains a Phenolic Inhibitor of the Histone Demethylase LSD1/KDM1A. Nutrients. 11 |
| Sendfeld F, Selga E, Scornik FS, et al. (2019) Experimental Models of Brugada syndrome. International Journal of Molecular Sciences. 20 |
| Selga E, Sendfeld F, Martinez-Moreno R, et al. (2017) Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient. Journal of Molecular and Cellular Cardiology |
| Peeters U, Scornik F, Riuró H, et al. (2015) Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. Circulation Journal : Official Journal of the Japanese Circulation Society. 79: 2118-29 |
| Wangüemert F, Bosch Calero C, Pérez C, et al. (2015) Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1636-43 |
| Riuró H, Campuzano O, Berne P, et al. (2015) Genetic analysis, in silico prediction, and family segregation in long QT syndrome. European Journal of Human Genetics : Ejhg. 23: 79-85 |
| Riuró H, Campuzano O, Arbelo E, et al. (2014) A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibility gene underlying long QT syndrome. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 1202-9 |