Хайлтын үр дүнгүүд - Gabriel Cáceres

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  1. 1
    Further Insights in the Most Common <i>SCN5A</i> Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

    Further Insights in the Most Common <i>SCN5A</i> Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect -н Christian Veltmann, Hector Barajas‐Martínez, Christian Wolpert, Martin Borggrefe, Rainer Schimpf, Ryan Pfeiffer, Gabriel Cáceres, Elena Burashnikov, Charles Antzelevitch, Dan Hu

    Хэвлэсэн 2016
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    Artigo
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  2. 2
    A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death

    A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death -н Eyal Nof, Jonathan M. Cordeiro, Guillermo J. Pérez, Fabiana S. Scornik, Kirstine Calløe, Barry A. Love, Elena Burashnikov, Gabriel Cáceres, Moshe Gunsburg, Charles Antzelevitch

    Хэвлэсэн 2010
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    Artigo
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  3. 3
    A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents

    A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents -н Dan Hu, Hector Barajas‐Martínez, Argelia Medeiros‐Domingo, Lia Crotti, Christian Veltmann, Rainer Schimpf, Janire Urrutia, Aintzane Alday, Óscar Casis, Ryan Pfeiffer, Elena Burashnikov, Gabriel Cáceres, David J. Tester, Christian Wolpert, Martin Borggrefe, Peter J. Schwartz, Michael J. Ackerman, Charles Antzelevitch

    Хэвлэсэн 2011
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    Artigo
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