Arama Sonuçları - Priori, Silvia
- Gösterilen 1 - 20 sonuçlar arası kayıtlar. 73
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1
Genetic testing to predict sudden cardiac death: current perspectives and future goals Yazar: Priori, Silvia G.
Baskı/Yayın Bilgisi 2014Metin -
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Brugada syndrome Yazar: Napolitano, Carlo, Priori, Silvia G
Baskı/Yayın Bilgisi 2006Metin -
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Inherited dysfunction of Sarcoplasmic Reticulum Ca(2+) Handling and Arrhythmogenesis Yazar: Priori, Silvia G, Chen, S. R. Wayne
Baskı/Yayın Bilgisi 2011Metin -
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ST‐Segment Elevation in the Setting of a Febrile Illness Yazar: Traub, Darren, Fonseka, Natasha, Priori, Silvia
Baskı/Yayın Bilgisi 2011Metin -
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Inherited conditions of arrhythmia: translating disease mechanisms to patient management Yazar: Priori, Silvia G, Remme, Carol Ann
Baskı/Yayın Bilgisi 2020Metin -
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Stabilizer Cell Gene Therapy: A Less-Is-More Strategy to Prevent Cardiac Arrhythmias Yazar: Liu, Michael B., Priori, Silvia, Qu, Zhilin, Weiss, James N.
Baskı/Yayın Bilgisi 2020Metin -
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Purkinje Cell Calcium Dysregulation Is the Cellular Mechanism that Underlies Catecholaminergic Polymorphic Ventricular Tachycardia Yazar: Herron, Todd J., Milstein, Michelle L., Anumonwo, Justus, Priori, Silvia G., Jalife, José
Baskı/Yayın Bilgisi 2010Metin -
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Y1767C, a novel SCN5A mutation, induces a persistent Na(+) current and potentiates ranolazine inhibition of Na(v)1.5 channels Yazar: Huang, Hai, Priori, Silvia G., Napolitano, Carlo, O'Leary, Michael E., Chahine, Mohamed
Baskı/Yayın Bilgisi 2011Metin -
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Prognostic value of first pass stress perfusion cardiac magnetic resonance in stable coronary artery disease Yazar: Catalano, Oronzo, Moro, Guido, Frascaroli, Mauro, Ceresa, Monica, Perotti, Mariarosa, Priori, Silvia G, Baldi, Maurizia
Baskı/Yayın Bilgisi 2011Metin -
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Digital transformation of major scientific meetings induced by the COVID-19 pandemic: insights from the ESC 2020 annual congress Yazar: Roffi, Marco, Casadei, Barbara, Gouillard, Christine, Nambatingué, Nata, Daval, Ghislain, Bardinet, Isabel, Priori, Silvia G
Baskı/Yayın Bilgisi 2021Metin -
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Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation Yazar: Grant, Augustus O., Carboni, Michael P., Neplioueva, Valentina, Starmer, C. Frank, Memmi, Mirella, Napolitano, Carlo, Priori, Silvia
Baskı/Yayın Bilgisi 2002Metin -
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Luminal Ca(2+) Regulation of Single Cardiac Ryanodine Receptors: Insights Provided by Calsequestrin and its Mutants Yazar: Qin, Jia, Valle, Giorgia, Nani, Alma, Nori, Alessandra, Rizzi, Nicoletta, Priori, Silvia G., Volpe, Pompeo, Fill, Michael
Baskı/Yayın Bilgisi 2008Metin -
18
Na(v)1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Na(v)1.5 on the surface of cardiomyocytes Yazar: Mohler, Peter J., Rivolta, Ilaria, Napolitano, Carlo, LeMaillet, Guy, Lambert, Stephen, Priori, Silvia G., Bennett, Vann
Baskı/Yayın Bilgisi 2004Metin -
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