Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Leonardo, Liberman"'
Publikováno v:
Multidisciplinary Business Review (2021)
This paper examines the relationship between intercultural competencies and performance in “international locals”, defined as employees who, albeit not formally appointed to any international position, are regularly exposed to different types of
Externí odkaz:
https://doaj.org/article/b0115a932703421c9fe26b3f5d13bec4
Publikováno v:
Pediatric Cardiology. 44:689-694
Background: The AliveCor KardiaMobile (ACKM) is a remote electrocardiogram (ECG) monitoring device. Little research has been conducted on its accuracy with pediatric patients. This prospective study aims to compare the ACKM six-lead device with a sta
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery.
Publikováno v:
Pediatric Cardiology. 43:218-224
Sudden cardiac arrest in pediatric patients is a rare occurrence. Supraventricular tachycardia without the presence of ventricular preexcitation in pediatric patients with a structurally normal heart is generally considered benign. Previous literatur
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 14, Iss 6, Pp 284-290 (2014)
Background: Radiofrequency catheter ablations of anteroseptal (AS) accessory pathways (AP) in pediatric patients have higher incidence of atrioventricular (AV) block than other AP locations. We report our experience using cryoablation in pediatric pa
Externí odkaz:
https://doaj.org/article/d5dc8328485c4d0ab6600004bbb6c334
Autor:
Leonardo Liberman
Publikováno v:
Innovar: Revista de Ciencias Administrativas y Sociales, Vol 24, Iss 53, Pp 187-196 (2014)
Although the use of a paternalistic style of management is widespread in the nonWestern context, it has only recently received attention from Western scholars. In this study, we compare the presence of a paternalistic style of management and delegat
Externí odkaz:
https://doaj.org/article/5b942db631d948dfba092a569b22c2e3
Publikováno v:
Pediatric Cardiology. 42:1350-1355
Block in accessory pathway (AP) conduction with adenosine has been previously described. However, conduction characteristics of these APs has not been well defined to date. All patients with APs
Autor:
Christina Y. Miyake, Erica J. Lay, Claudia Soler-Alfonso, Kevin E. Glinton, Kimberly M. Houck, Mustafa Tosur, Nancy E. Moran, Sara B. Stephens, Fernando Scaglia, Taylor S. Howard, Jeffrey J. Kim, Tam Dam Pham, Santiago O. Valdes, Na Li, Chaya N. Murali, Lilei Zhang, Maina Kava, Deane Yim, Cheyenne Beach, Gregory Webster, Leonardo Liberman, Christopher M. Janson, Prince J. Kannankeril, Samantha Baxter, Moriel Singer-Berk, Jordan Wood, Samuel J. Mackenzie, Michael Sacher, Lina Ghaloul-Gonzalez, Claudia Pedroza, Shaine A. Morris, Saad A. Ehsan, Mahshid S. Azamian, Seema R. Lalani
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics.
TANGO2 deficiency disorder (TDD), an autosomal recessive disease first reported in 2016, is characterized by neurodevelopmental delays, seizures, intermittent ataxia, hypothyroidism and life-threatening metabolic and cardiac crises. The purpose of th
Autor:
Marine Tortigue, Lynne E. Nield, Matilde Karakachoff, Christopher J. McLeod, Emre Belli, Sonya V. Babu-Narayan, Solène Prigent, Angèle Boet, Miriam Conway, Robert W. Elder, Magalie Ladouceur, Paul Khairy, Ewa Kowalik, David M. Kalfa, David J. Barron, Shafi Mussa, Anita Hiippala, Joel Temple, Sylvia Abadir, Laurianne Le Gloan, Matthias Lachaud, Shubhayan Sanatani, Jean-Benoit Thambo, Céline Grunenwald Gronier, Pascal Amedro, Guy Vaksmann, Anne Charbonneau, Linda Koutbi, Caroline Ovaert, Ali Houeijeh, Nicolas Combes, Philippe Maury, Guillaume Duthoit, Bérengère Hiel, Christopher C. Erickson, Caroline Bonnet, George F. Van Hare, Christian Dina, Clément Karsenty, Emmanuelle Fournier, Mathieu Le Bloa, Robert H. Pass, Leonardo Liberman, Juha-Matti Happonen, James C. Perry, Bénédicte Romefort, Nadir Benbrik, Quentin Hauet, Alain Fraisse, Michael A. Gatzoulis, Dominic J. Abrams, Anne M. Dubin, Siew Yen Ho, Richard Redon, Emile A. Bacha, Jean-Jacques Schott, Alban-Elouen Baruteau
Publikováno v:
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine, 2022, 15 (3), ⟨10.1161/CIRCGEN.121.003464⟩
Circulation: Genomic and Precision Medicine, 2022, 15 (3), ⟨10.1161/CIRCGEN.121.003464⟩
Background: Congenitally corrected transposition of the great arteries (ccTGA) is a rare disease of unknown cause. We aimed to better understand familial recurrence patterns. Methods: An international, multicentre, retrospective cohort study was cond
Publikováno v:
Pediatric Cardiology. 42:109-115
Definitive treatment of supraventricular tachycardia (SVT) substrate involves catheter ablation. While objective success rates have been well established, long-term subjective patient experiences have not been well described. We quantify a subjective