These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
130 related items for PubMed ID: 28605744
1. A Clinical Case of Catecholaminergic Polymorphic Ventricular Tachycardia: The Clinical Suspicious and the Need of Genetics. Del Franco A, Gualandi F, Malagù M, Ferlini A, Xiao D, Ferrari R, Bertini M. Cardiology; 2017; 138(2):69-72. PubMed ID: 28605744 [Abstract] [Full Text] [Related]
2. A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia. Bosch C, Campuzano O, Sarquella-Brugada G, Cesar S, Perez-Serra A, Coll M, Mademont I, Mates J, Del Olmo B, Iglesias A, Brugada J, Petersen V, Brugada R. Forensic Sci Int; 2017 Jan; 270():173-177. PubMed ID: 27988446 [Abstract] [Full Text] [Related]
14. Slowed depolarization and irregular repolarization in catecholaminergic polymorphic ventricular tachycardia: a study from cellular Ca2+ transients and action potentials to clinical monophasic action potentials and electrocardiography. Paavola J, Väänänen H, Larsson K, Penttinen K, Toivonen L, Kontula K, Laine M, Aalto-Setälä K, Swan H, Viitasalo M. Europace; 2016 Oct; 18(10):1599-1607. PubMed ID: 26705554 [Abstract] [Full Text] [Related]
15. Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: A Translational Perspective for the Clinician-Scientist. Kallas D, Lamba A, Roston TM, Arslanova A, Franciosi S, Tibbits GF, Sanatani S. Int J Mol Sci; 2021 Aug 27; 22(17):. PubMed ID: 34502196 [Abstract] [Full Text] [Related]
16. High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening. Haugaa KH, Leren IS, Berge KE, Bathen J, Loennechen JP, Anfinsen OG, Früh A, Edvardsen T, Kongsgård E, Leren TP, Amlie JP. Europace; 2010 Mar 27; 12(3):417-23. PubMed ID: 20106799 [Abstract] [Full Text] [Related]
17. Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia. Wangüemert F, Bosch Calero C, Pérez C, Campuzano O, Beltran-Alvarez P, Scornik FS, Iglesias A, Berne P, Allegue C, Ruiz Hernandez PM, Brugada J, Pérez GJ, Brugada R. Heart Rhythm; 2015 Jul 27; 12(7):1636-43. PubMed ID: 25814417 [Abstract] [Full Text] [Related]