Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 17 (of 17 Records) |
Query Trace: Arrhythmogenic Right Ventricular Dysplasia[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 |
Mutations of plakophilin-2 in Chinese with arrhythmogenic right ventricular dysplasia/cardiomyopathy. The American journal of cardiology 2009 May 103 (10): 1439-44. Qiu Xiaoliang, Liu Wenling, Hu Dayi, Zhu Tiangang, Li Cuilan, Li Lei, Guo Chengjun, Liu Xingpeng, Wang Lei, Zheng Hua, Wang Chunling, Diao Qing, Shi Dan, Zhan Pingyun, Deng Yuanming, Liu Kunshen, Wang Yi, Liu Baomin, Liu Hongming, Zhang |
Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. Cardiovascular genetics 2009 Oct 2 (5): 428-35. den Haan A Dénise, Tan Boon Yew, Zikusoka Michelle N, Lladó Laura Ibañez, Jain Rahul, Daly Amy, Tichnell Crystal, James Cynthia, Amat-Alarcon Nuria, Abraham Theodore, Russell Stuart D, Bluemke David A, Calkins Hugh, Dalal Darshan, Judge Daniel |
Desmoglein-2 and desmocollin-2 mutations in dutch arrhythmogenic right ventricular dysplasia/cardiomypathy patients: results from a multicenter study. Circulation. Cardiovascular genetics 2009 Oct 2 (5): 418-27. Bhuiyan Zahurul A, Jongbloed Jan D H, van der Smagt Jasper, Lombardi Paola M, Wiesfeld Ans C P, Nelen Marcel, Schouten Meyke, Jongbloed Roselie, Cox Moniek G P J, van Wolferen Marleen, Rodriguez Luz M, van Gelder Isabelle C, Bikker Hennie, Suurmeijer Albert J H, van den Berg Maarten P, Mannens Marcel M A M, Hauer Richard N W, Wilde Arthur A M, van Tintelen J Pet |
Angiotensin-converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia: is DD genotype helpful in predicting syncope risk? Journal of the renin-angiotensin-aldosterone system : JRAAS 2008 Dec 9 (4): 215-20. Ozben Beste, Altun Ibrahim, Sabri Hancer Veysel, Bilge Ahmet Kaya, Tanrikulu Azra Meryem, Diz-Kucukkaya Reyhan, Fak Ali Serdar, Yilmaz Ercument, Adalet Kam |
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice. 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 2010 Jun 12 (6): 861-8. Fressart Veronique, Duthoit Guillaume, Donal Erwan, Probst Vincent, Deharo Jean-Claude, Chevalier Philippe, Klug Didier, Dubourg Olivier, Delacretaz Etienne, Cosnay Pierre, Scanu Patrice, Extramiana Fabrice, Keller Dagmar, Hidden-Lucet Françoise, Simon Françoise, Bessirard Vanessa, Roux-Buisson Nathalie, Hebert Jean-Louis, Azarine Arshid, Casset-Senon Daniele, Rouzet François, Lecarpentier Yves, Fontaine Guy, Coirault Catherine, Frank Robert, Hainque Bernard, Charron Philip |
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 |
RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort. PloS one 2014 9 (6): e101059. Akilzhanova Ainur, Guelly Christian, Nuralinov Omirbek, Nurkina Zhannur, Nazhat Dinara, Smagulov Shalkhar, Tursunbekov Azat, Alzhanova Anar, Rashbayeva Gulzhaina, Abdrakhmanov Ayan, Dosmagambet Sholpan, Trajanoski Slave, Zhumadilov Zhaxybay, Sharman Almaz, Bekbosynova Mahabb |
Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers. European heart journal 2015 Apr 36 (14): 847-55. Bhonsale Aditya, Groeneweg Judith A, James Cynthia A, Dooijes Dennis, Tichnell Crystal, Jongbloed Jan D H, Murray Brittney, te Riele Anneline S J M, van den Berg Maarten P, Bikker Hennie, Atsma Douwe E, de Groot Natasja M, Houweling Arjan C, van der Heijden Jeroen F, Russell Stuart D, Doevendans Pieter A, van Veen Toon A, Tandri Harikrishna, Wilde Arthur A, Judge Daniel P, van Tintelen J Peter, Calkins Hugh, Hauer Richard |
Influence of Genotype on Structural Atrial Abnormalities and Atrial Fibrillation or Flutter in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. Journal of cardiovascular electrophysiology 2016 Aug . Bourfiss Mimount, Te Riele Anneline S J M, Mast Thomas P, Cramer Maarten J, VAN DER Heijden Jeroen F, VAN Veen Toon A B, Loh Peter, Dooijes Dennis, Hauer Richard N W, Velthuis Birgitta |
Genetic mutations in young patients admitted to an emergency department for syncope during sport practice. Medicina clinica 2018 4 151 (7): 270-274. Gómez Alcaraz Jorge, Bustamante José, Corral Ervigio, Casado Florez Maria Isabel, Vivas David, Cañadas-Godoy Victoria, González Del Castillo Juan, González Armengol Juan Jorge, López-Farré Antonio, Martín Sánchez Francisco Javi |
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience. Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349. Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C |
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 |
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia. Frontiers in neuroscience 2021 4 15 629610. Ma Mei-Gang, Liu Xiao-Rong, Wu Yuan, Wang Jie, Li Bing-Mei, Shi Yi-Wu, Su Tao, Li Bin, Liu De-Tian, Yi Yong-Hong, Liao Wei-Pi |
Genetic profile and genotype-phenotype correlations in childhood cardiomyopathy. Archives of cardiovascular diseases 2023 5 . Chloé Wanert, Fedoua El Louali, Sarab Al Dybiat, Karine Nguyen, Stéphane Zaffran, Caroline Ovae |
Correlations Between Endocardial Voltage Mapping, Diagnosis, and Genetics in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy. The American journal of cardiology 2023 1 190 113-120. Delasnerie Hubert, Gandjbakhch Estelle, Sauve Romain, Beneyto Maxime, Domain Guillaume, Voglimacci-Stephanopoli Quentin, Mandel Franck, Badenco Nicolas, Waintraub Xavier, Mondoly Pierre, Fressart Véronique, Rollin Anne, Maury Philip |
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- Page last updated:Apr 22, 2024
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