Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Abnormalities and PKP2[original query] |
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Arrhythmogenic right ventricular dysplasia. Transactions of the American Clinical and Climatological Association 2008 119 273-86; discussion 287-8. Calkins Hu |
Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnostic task force criteria: impact of new task force criteria. Circulation. Arrhythmia and electrophysiology 2010 Apr 3 (2): 126-33. Cox Moniek G P J, van der Smagt Jasper J, Noorman Maartje, Wiesfeld Ans C, Volders Paul G A, van Langen Irene M, Atsma Douwe E, Dooijes Dennis, Houweling Arjan C, Loh Peter, Jordaens Luc, Arens Yvonne, Cramer Maarten J, Doevendans Pieter A, van Tintelen J Peter, Wilde Arthur A M, Hauer Richard N |
Arrhythmogenic right ventricular dysplasia/cardiomyopathy according to revised 2010 task force criteria with inclusion of non-desmosomal phospholamban mutation carriers. The American journal of cardiology 2013 Oct 112 (8): 1197-206. Groeneweg Judith A, van der Zwaag Paul A, Olde Nordkamp Louise R A, Bikker Hennie, Jongbloed Jan D H, Jongbloed Roselie, Wiesfeld Ans C P, Cox Moniek G P J, van der Heijden Jeroen F, Atsma Douwe E, de Boer Karin, Doevendans Pieter A, Vink Aryan, van Veen Toon A B, Dooijes Dennis, van den Berg Maarten P, Wilde Arthur A M, van Tintelen J Peter, Hauer Richard |
Quantitative analysis of PKP2 and neighbouring genes in a patient with arrhythmogenic right ventricular cardiomyopathy caused by heterozygous PKP2 deletion. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2017 Apr 19 (4): 644-650. Sonoda Keiko, Ohno Seiko, Otuki Sou, Kato Koichi, Yagihara Nobue, Watanabe Hiroshi, Makiyama Takeru, Minamino Tohru, Horie Mino |
PKP2 and DSG2 genetic variations in Latvian arrhythmogenic right ventricular dysplasia/cardiomyopathy registry patients. Anatolian journal of cardiology 2018 11 20 (5): 296-302. Bidina Luize, Kupics Kaspars, Sokolova Emma, Pavlovics Mihails, Dobele Zane, Caunite Laima, Kalejs Oskars, Gailite Lin |
Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2019 4 32 (9): 1281-1290. Hata Yukiko, Hirono Keiichi, Yamaguchi Yoshiaki, Ichida Fukiko, Oku Yuko, Nishida Nao |
Phenotypic Variability of a Pathogenic PKP2 Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport Restriction. Frontiers in cardiovascular medicine 2021 6 8 635141. Leone Maria Pia, Palumbo Pietro, Saenen Johan, Mastroianno Sandra, Castellana Stefano, Amico Cesare, Mazza Tommaso, Potenza Domenico Rosario, Petracca Antonio, Castori Marco, Carella Massimo, Di Stolfo Giusep |
Role of genetic testing in young patients with idiopathic atrioventricular conduction disease. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 11 25 (2): 643-650. Auricchio Angelo, Demarchi Andrea, Özkartal Tardu, Campanale Daniela, Caputo Maria Luce, di Valentino Marcello, Menafoglio Andrea, Regoli Francois, Facchini Marco, Del Bufalo Alessandro, Foglia Pietro, Ferrari Nicola, Bomio Fulvio, Medeiros-Domingo Argelia, Moccetti Tiziano, Pedrazzini Giovanni B, Klersy Catherine, Conte Giul |
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