Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Abnormalities and MYBPC3[original query] |
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Mutations profile in Chinese patients with hypertrophic cardiomyopathy. Clinica chimica acta; international journal of clinical chemistry 2005 Jan 351 (1-2): 209-16. Song Lei, Zou Yubao, Wang Jizheng, Wang Zhimin, Zhen Yisong, Lou Kejia, Zhang Qian, Wang Xiaojian, Wang Hu, Li Jia, Hui Rut |
Diastolic abnormalities as the first feature of hypertrophic cardiomyopathy in Dutch myosin-binding protein C founder mutations. JACC. Cardiovascular imaging 2009 Jan 2 (1): 58-64. Michels Michelle, Soliman Osama I I, Kofflard Marcel J, Hoedemaekers Yvonne M, Dooijes Dennis, Majoor-Krakauer Danielle, ten Cate Folkert |
Subclinical echocardiographic abnormalities in phenotype-negative carriers of myosin-binding protein C3 gene mutation for hypertrophic cardiomyopathy. American heart journal 2011 Aug 162 (2): 262-267.e3. De Sabe, Borowski Allen G, Wang Heng, Nye Leah, Xin Baozhong, Thomas James D, Tang W H Wils |
MYBPC3 hypertrophic cardiomyopathy can be detected by using advanced ECG in children and young adults. Journal of electrocardiology 2016 Mar . Fernlund E, Liuba P, Carlson J, Platonov P G, Schlegel T |
Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations. Journal of electrocardiology 2018 12 51 (6): 983-989. Jalanko Mikko, Heliö Tiina, Mustonen Pirjo, Kokkonen Jorma, Huhtala Heini, Laine Mika, Jääskeläinen Pertti, Tarkiainen Mika, Lauerma Kirsi, Sipola Petri, Laakso Markku, Kuusisto Johanna, Nikus Kje |
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 |
Hypertrophic cardiomyopathy in myosin-binding protein C (MYBPC3) Icelandic founder mutation carriers. Open heart 2020 4 7 (1): e001220. Adalsteinsdottir Berglind, Burke Michael, Maron Barry J, Danielsen Ragnar, Lopez Begoña, Diez Javier, Jarolim Petr, Seidman Jonathan, Seidman Christine E, Ho Carolyn Y, Gunnarsson Gunnar |
Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy. BMC cardiovascular disorders 2020 12 20 (1): 516. Velicki Lazar, Jakovljevic Djordje G, Preveden Andrej, Golubovic Miodrag, Bjelobrk Marija, Ilic Aleksandra, Stojsic Snezana, Barlocco Fausto, Tafelmeier Maria, Okwose Nduka, Tesic Milorad, Brennan Paul, Popovic Dejana, Ristic Arsen, MacGowan Guy A, Filipovic Nenad, Maier Lars S, Olivotto Iaco |
Implications of structural right ventricular involvement in patients with hypertrophic cardiomyopathy. European heart journal. Quality of care & clinical outcomes 2022 2 9 (1): 34-41. Zhang Yu, Zhu Yuming, Zhang Mo, Liu Jie, Wu Guixin, Wang Jizheng, Sun Xiaolu, Wang Dong, Jiang Wen, Xu Lianjun, Kang Lianming, Song L |
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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- Page last updated:Apr 22, 2024
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