about
A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.Short QT syndrome in pediatrics.Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.Large Genomic Imbalances in Brugada Syndrome.Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic InvestigationGenetics of inherited arrhythmias in pediatrics.Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?Genetic basis of dilated cardiomyopathy.Post-mortem genetic analysis in juvenile cases of sudden cardiac death.Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis.A Genetically Vulnerable Myocardium May Predispose to Myocarditis.Cardiac and mitochondrial function in HIV-uninfected fetuses exposed to antiretroviral treatmentPalliative switch: a surgical decision after hybrid procedureShort QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare VariantsElectrocardiogram in Newborns: Beneficial or Not?Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
@nl
type
label
Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
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Sergi Cesar
@nl
P106
P1153
56414745100
P31
P496
0000-0002-2798-1756