Your search returned 651 results.

Results
	641.	Novel α-Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical-Pathologic Correlation. [electronic resource] by Frustaci, Andrea De Luca, Alessandro Guida, Valentina Biagini, Tommaso Mazza, Tommaso Gaudio, Carlo Letizia, Claudio Russo, Matteo Antonio Galea, Nicola Chimenti, Cristina Producer: 20191022 In: Journal of the American Heart Association vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	642.	A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction. [electronic resource] by Wang, Ce Hata, Yukiko Hirono, Keiichi Takasaki, Asami Ozawa, Sayaka Watanabe Nakaoka, Hideyuki Saito, Kazuyoshi Miyao, Nariaki Okabe, Mako Ibuki, Keijiro Nishida, Naoki Origasa, Hideki Yu, Xianyi Bowles, Neil E Ichida, Fukiko Producer: 20180514 In: Journal of the American Heart Association vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	643.	Videoscopic left cardiac sympathetic denervation for patients with recurrent ventricular fibrillation/malignant ventricular arrhythmia syndromes besides congenital long-QT syndrome. [electronic resource] by Coleman, Mira A Bos, J Martijn Johnson, Jonathan N Owen, Heidi J Deschamps, Claude Moir, Christopher Ackerman, Michael J Producer: 20121026 In: Circulation. Arrhythmia and electrophysiology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	644.	Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction. [electronic resource] by Ohno, Seiko Omura, Masato Kawamura, Mihoko Kimura, Hiromi Itoh, Hideki Makiyama, Takeru Ushinohama, Hiroya Makita, Naomasa Horie, Minoru Producer: 20150629 In: 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 vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	645.	Cardiovascular magnetic resonance characterization of left ventricular non-compaction provides independent prognostic information in patients with incident heart failure or suspected cardiomyopathy. [electronic resource] by Ashrith, Guha Gupta, Dipti Hanmer, Janel Weiss, Robert M Producer: 20150824 In: Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	646.	A novel lamin A/C gene missense mutation (445 V > E) in immunoglobulin-like fold associated with left ventricular non-compaction. [electronic resource] by Liu, Zhouying Shan, Hong Huang, Jian Li, Ning Hou, Cuihong Pu, Jielin Producer: 20170315 In: 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 vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	647.	Isolated left ventricular noncompaction: clinical profile and prognosis in 106 adult patients. [electronic resource] by Tian, Tao Liu, Yaxin Gao, Linggen Wang, Jizheng Sun, Kai Zou, Yubao Wang, Linping Zhang, Lin Li, Yuehua Xiao, Yan Song, Lei Zhou, Xianliang Producer: 20150522 In: Heart and vessels vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	648.	Co-Phenotype of Left Ventricular Non-Compaction Cardiomyopathy and Atypical Catecholaminergic Polymorphic Ventricular Tachycardia in Association With R169Q, a Ryanodine Receptor Type 2 Missense Mutation. [electronic resource] by Nozaki, Yoshihiro Kato, Yoshiaki Uike, Kiyoshi Yamamura, Kenichiro Kikuchi, Masahiro Yasuda, Maki Ohno, Seiko Horie, Minoru Murayama, Takashi Kurebayashi, Nagomi Horigome, Hitoshi Producer: 20201019 In: Circulation journal : official journal of the Japanese Circulation Society vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	649.	Isolated left ventricular noncompaction in sub-Saharan Africa: a clinical and echocardiographic perspective. [electronic resource] by Peters, Ferande Khandheria, Bijoy K dos Santos, Claudia Matioda, Hiral Maharaj, Nirvarthi Libhaber, Elena Mamdoo, Farouk Essop, Mohammed R Producer: 20120510 In: Circulation. Cardiovascular imaging vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	650.	Prevalence and Prognostic Significance of Left Ventricular Noncompaction in Patients Referred for Cardiac Magnetic Resonance Imaging. [electronic resource] by Ivanov, Alexander Dabiesingh, Devindra S Bhumireddy, Geetha P Mohamed, Ambreen Asfour, Ahmed Briggs, William M Ho, Jean Khan, Saadat A Grossman, Alexandra Klem, Igor Sacchi, Terrence J Heitner, John F Producer: 20170925 In: Circulation. Cardiovascular imaging vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	651.	Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. [electronic resource] by Hastings, Robert de Villiers, Carin P Hooper, Charlotte Ormondroyd, Liz Pagnamenta, Alistair Lise, Stefano Salatino, Silvia Knight, Samantha J L Taylor, Jenny C Thomson, Kate L Arnold, Linda Chatziefthimiou, Spyros D Konarev, Petr V Wilmanns, Matthias Ehler, Elisabeth Ghisleni, Andrea Gautel, Mathias Blair, Edward Watkins, Hugh Gehmlich, Katja Producer: 20171030 In: Circulation. Cardiovascular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
24
25
26
27
28
29
30
31
32
33