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KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation.
González-Garrido A, López-Ramírez O, Cerda-Mireles A, Navarrete-Miranda T, Flores-Arenas AI, Rojo-Domínguez A, Arregui L, Iturralde P, Antúnez-Argüelles E, Domínguez-Pérez M, Jacobo-Albavera L, Carnevale A, Villarreal-Molina T. González-Garrido A, et al. Among authors: iturralde p. Int J Mol Sci. 2024 Jan 12;25(2):953. doi: 10.3390/ijms25020953. Int J Mol Sci. 2024. PMID: 38256028 Free PMC article.
Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression.
González-Garrido A, Domínguez-Pérez M, Jacobo-Albavera L, López-Ramírez O, Guevara-Chávez JG, Zepeda-García O, Iturralde P, Carnevale A, Villarreal-Molina T. González-Garrido A, et al. Among authors: iturralde p. Front Cardiovasc Med. 2021 Feb 22;8:625449. doi: 10.3389/fcvm.2021.625449. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 33693037 Free PMC article.
Diagnostic challenges of Brugada Syndrome in pediatric patients.
Manzano-Cabada J, Reyes-Quintero ÁE, Chávez-Gutiérrez CA, Gómez-Flores J, Colín-Lizalde L, Morales JL, Nava S, Iturralde P, Márquez MF. Manzano-Cabada J, et al. Among authors: iturralde p. J Electrocardiol. 2020 May-Jun;60:72-76. doi: 10.1016/j.jelectrocard.2020.03.012. Epub 2020 Mar 31. J Electrocardiol. 2020. PMID: 32304903
109 results