Author: "Valdivia, A. R." / Publisher: ovid technologies (wolters kluwer health) - Searchworks@Jio Institute Digital Library Search Results

1. Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation

Author: Yin, Liheng, primary, Zahradnikova, Alexandra, additional, Rizzetto, Riccardo, additional, Boncompagni, Simona, additional, Rabesahala de Meritens, Camille, additional, Zhang, Yadan, additional, Joanne, Pierre, additional, Marqués-Sulé, Elena, additional, Aguilar-Sánchez, Yuriana, additional, Fernández-Tenorio, Miguel, additional, Villejoubert, Olivier, additional, Li, Linwei, additional, Wang, Yue Yi, additional, Mateo, Philippe, additional, Nicolas, Valérie, additional, Gerbaud, Pascale, additional, Lai, F. Anthony, additional, Perrier, Romain, additional, Álvarez, Julio L., additional, Niggli, Ernst, additional, Valdivia, Héctor H., additional, Valdivia, Carmen R., additional, Ramos-Franco, Josefina, additional, Zorio, Esther, additional, Zissimopoulos, Spyros, additional, Protasi, Feliciano, additional, Benitah, Jean-Pierre, additional, and Gómez, Ana M., additional
Published: 2021
Full Text: View/download PDF

2. Hospital-wide Implementation of Standardized Access to Peripheral Vasopressors for Sepsis

Author: Farris, Reid, primary, Linggi Irby, Gretchen Ann, additional, Valdivia, Hector R., additional, Kalember, Lauren, additional, Beardsley, Elaine, additional, O’Hare, Pauline, additional, Clifton, Holly, additional, Rutman, Lori, additional, and Roberts, Joan S., additional
Published: 2019
Full Text: View/download PDF

3. Determining Interrater Reliability of the Cornell Assessment of Pediatric Delirium Screening Tool Among PICU Nurses

Author: Valdivia, Hector R., primary and Carlin, Kristen E., additional
Published: 2019
Full Text: View/download PDF

4. Cardiac Kir2.1 and Na V 1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

Author: Ponce-Balbuena, Daniela, primary, Guerrero-Serna, Guadalupe, additional, Valdivia, Carmen R., additional, Caballero, Ricardo, additional, Diez-Guerra, F. Javier, additional, Jiménez-Vázquez, Eric N., additional, Ramírez, Rafael J., additional, Monteiro da Rocha, André, additional, Herron, Todd J., additional, Campbell, Katherine F., additional, Willis, B. Cicero, additional, Alvarado, Francisco J., additional, Zarzoso, Manuel, additional, Kaur, Kuljeet, additional, Pérez-Hernández, Marta, additional, Matamoros, Marcos, additional, Valdivia, Héctor H., additional, Delpón, Eva, additional, and Jalife, José, additional
Published: 2018
Full Text: View/download PDF

5. Navigating the Sea of Long Noncoding RNAs

Author: Alvarado, Francisco J., primary, Valdivia, Carmen R., additional, and Valdivia, Héctor H., additional
Published: 2018
Full Text: View/download PDF

6. Atrial Infarction-Induced Spontaneous Focal Discharges and Atrial Fibrillation in Sheep

Author: Avula, Uma Mahesh R., primary, Hernandez, Jonathan J., additional, Yamazaki, Masatoshi, additional, Valdivia, Carmen R., additional, Chu, Antony, additional, Rojas-Pena, Alvaro, additional, Kaur, Kuljeet, additional, Ramos-Mondragón, Roberto, additional, Anumonwo, Justus M., additional, Nattel, Stanley, additional, Valdivia, Héctor H., additional, and Kalifa, Jérôme, additional
Published: 2018
Full Text: View/download PDF

7. Enhanced Classification of Brugada Syndrome–Associated and Long-QT Syndrome–Associated Genetic Variants in the SCN5A -Encoded Na v 1.5 Cardiac Sodium Channel

Author: Kapplinger, Jamie D., primary, Giudicessi, John R., additional, Ye, Dan, additional, Tester, David J., additional, Callis, Thomas E., additional, Valdivia, Carmen R., additional, Makielski, Jonathan C., additional, Wilde, Arthur A., additional, and Ackerman, Michael J., additional
Published: 2015
Full Text: View/download PDF

8. Abstract 18946: A Complex Cardiac Rhythm and Conduction Abnormalities in Three Families Carrying a SCN5A Missense Mutation May Involve Single Nucleotide Polymorphisms in SCN5A and RYR2 genes

Author: Antunez-Arguelles, Erika, primary, Medeiros-Domingo, Argelia, additional, Villarreal, Teresa, additional, Hernandez, Jonathan J, additional, Iturralde, Pedro, additional, Valdivia, Hector H, additional, Makielski, Jonathan C, additional, and Valdivia, Carmen R, additional
Published: 2014
Full Text: View/download PDF

9. Abstract 19541: Impaired Calcium Release, Prolonged Action Potentials and Early Afterdepolarizations in Ventricular Myocytes from Mice Harboring a Ryanodine Receptor 2 Loss-of-Function Mutation Associated with Catecholaminergic Polymorphic Ventricular Tachycardia

Author: Zhao, Yan-Ting, primary, Loaiza, Randall, additional, Valdivia, Carmen R, additional, Alvarado, Francisco, additional, Li, Cong, additional, Powers, Patricia, additional, and Valdivia, Héctor H, additional
Published: 2012
Full Text: View/download PDF

10. Abstract 5317: Identification and Characterization of a Novel Susceptibility Gene, SCN3B, for Idiopathic Ventricular Fibrillation

Author: Valdivia, Carmen R, primary, Mereidos-Domingo, Argelia, additional, Algiers, Thimothy J, additional, Ackerman, Michael J, additional, and Makielski, Jonathan C, additional
Published: 2008
Full Text: View/download PDF

11. Abstract 3090: Missense Mutations in SNTA1-Encoded Syntrophin Alpha and Sudden Infant Death Syndrome

Author: Van Norstrand, David W, primary, Medeiros-Domingo, Argelia, additional, Tester, David J, additional, Cheng, Jianding, additional, Valdivia, Carmen R, additional, Makielski, Jonathan C, additional, and Ackerman, Michael J, additional
Published: 2008
Full Text: View/download PDF

12. Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Mutations in Sudden Infant Death Syndrome

Author: Van Norstrand, David W., primary, Valdivia, Carmen R., additional, Tester, David J., additional, Ueda, Kazuo, additional, London, Barry, additional, Makielski, Jonathan C., additional, and Ackerman, Michael J., additional
Published: 2007
Full Text: View/download PDF

13. Abstract 2968: Postmortem Genetic Testing of the GPD1-L-Encoded Glycerol-3-Phosphate Dehydrogenase 1-Like Protein in Sudden Infant Death Syndrome

Author: Van Norstrand, David W, primary, Valdivia, Carmen R, additional, Tester, David J, additional, Ueda, Kazuo, additional, London, Barry, additional, Makielski, Jonathan C, additional, and Ackerman, Michael J, additional
Published: 2007
Full Text: View/download PDF

14. A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels

Author: Makielski, Jonathan C., primary, Ye, Bin, additional, Valdivia, Carmen R., additional, Pagel, Matthew D., additional, Pu, Jielin, additional, Tester, David J., additional, and Ackerman, Michael J., additional
Published: 2003
Full Text: View/download PDF

15. Cysticercosis presenting as a subdural hematoma

Author: Feinberg, W. M., primary and Valdivia, F. R., additional
Published: 1984
Full Text: View/download PDF

Searchworks

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources

Refine your results

15 results on '"Valdivia, A. R."'

1. Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation

2. Hospital-wide Implementation of Standardized Access to Peripheral Vasopressors for Sepsis

3. Determining Interrater Reliability of the Cornell Assessment of Pediatric Delirium Screening Tool Among PICU Nurses

4. Cardiac Kir2.1 and Na V 1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

5. Navigating the Sea of Long Noncoding RNAs

6. Atrial Infarction-Induced Spontaneous Focal Discharges and Atrial Fibrillation in Sheep

7. Enhanced Classification of Brugada Syndrome–Associated and Long-QT Syndrome–Associated Genetic Variants in the SCN5A -Encoded Na v 1.5 Cardiac Sodium Channel

8. Abstract 18946: A Complex Cardiac Rhythm and Conduction Abnormalities in Three Families Carrying a SCN5A Missense Mutation May Involve Single Nucleotide Polymorphisms in SCN5A and RYR2 genes

9. Abstract 19541: Impaired Calcium Release, Prolonged Action Potentials and Early Afterdepolarizations in Ventricular Myocytes from Mice Harboring a Ryanodine Receptor 2 Loss-of-Function Mutation Associated with Catecholaminergic Polymorphic Ventricular Tachycardia

10. Abstract 5317: Identification and Characterization of a Novel Susceptibility Gene, SCN3B, for Idiopathic Ventricular Fibrillation

11. Abstract 3090: Missense Mutations in SNTA1-Encoded Syntrophin Alpha and Sudden Infant Death Syndrome

12. Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Mutations in Sudden Infant Death Syndrome

13. Abstract 2968: Postmortem Genetic Testing of the GPD1-L-Encoded Glycerol-3-Phosphate Dehydrogenase 1-Like Protein in Sudden Infant Death Syndrome

14. A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels

15. Cysticercosis presenting as a subdural hematoma

Catalog

Searchworks

Select search scope, currently: Articles Catalog books, media & more in Jio Institute collections Articles journal articles & other e-resources

Search

Search Constraints

Refine your results

Search Limiters

Publication Year Range

Journal

Database

15 results on '"Valdivia, A. R."'

Search Results

Catalog

Select search scope, currently: Articles

Catalog

books, media & more in Jio Institute collections

Articles

journal articles & other e-resources