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Items: 1 to 20 of 21

1.
NMR-Based Metabolomic Analysis of Sera in Mouse Models of CVB3-Induced Viral Myocarditis and Dilated Cardiomyopathy
Qing Kong, Jinping Gu, Ruohan Lu, Caihua Huang, Xiaomin Hu, Weifeng Wu, Donghai Lin
Biomolecules. 2022 Jan; 12(1): 112. Published online 2022 Jan 11. doi: 10.3390/biom12010112
PMCID:
PMC8773787
ArticlePubReaderPDF–2.3MCite
2.
Protective action of tetramethylpyrazine phosphate against dilated cardiomyopathy in cTnTR141W transgenic mice
Hai-ping Zhao, Dan Lü, Wei Zhang, Li Zhang, Shu-mei Wang, Chun-mei Ma, Chuan Qin, Lian-feng Zhang
Acta Pharmacol Sin. 2010 Mar; 31(3): 281–288. Published online 2010 Feb 15. doi: 10.1038/aps.2010.6
PMCID:
PMC4002419
ArticlePubReaderPDF–4.4MCite
3.
Impaired Cardiomyocyte Maturation Leading to DCM: A Case Report and Literature Review
Letao Zhou, Jinglan Huang, Hong Li, Hongyu Duan, Yimin Hua, Yuxuan Guo, Kaiyu Zhou, Yifei Li
Medicina (Kaunas) 2023 Jun; 59(6): 1158. Published online 2023 Jun 16. doi: 10.3390/medicina59061158
PMCID:
PMC10303204
ArticlePubReaderPDF–3.4MCite
4.
Longitudinal Observational Study of Cardiac Outcome Risk Factor Prediction in Children, Adolescents, and Adults with Barth Syndrome
Shahryar Chowdhury, Lanier Jackson, Barry J. Byrne, Randall M. Bryant, W. Todd Cade, Tammy Lane Churchill, Julia Buchanan, Carolyn Taylor
Pediatr Cardiol. Author manuscript; available in PMC 2023 Aug 1.
Published in final edited form as: Pediatr Cardiol. 2022 Aug; 43(6): 1251–1263. Published online 2022 Mar 3. doi: 10.1007/s00246-022-02846-8
PMCID:
PMC9462389
ArticlePubReaderPDF–1.3MCite
5.
Genetic Testing in Pediatric Left Ventricular Noncompaction
Erin M. Miller, Robert B. Hinton, Richard Czosek, Angela Lorts, Ashley Parrott, Amy R. Shikany, Richard F. Ittenbach, Stephanie M. Ware
Circ Cardiovasc Genet. Author manuscript; available in PMC 2021 Sep 9.
Published in final edited form as: Circ Cardiovasc Genet. 2017 Dec; 10(6): e001735. doi: 10.1161/CIRCGENETICS.117.001735
PMCID:
PMC8428628
ArticlePubReaderPDF–994KCite
6.
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
Francesco Mazzarotto, Megan H. Hawley, Matteo Beltrami, Leander Beekman, Antonio de Marvao, Kathryn A. McGurk, Ben Statton, Beatrice Boschi, Francesca Girolami, Angharad M. Roberts, Elisabeth M. Lodder, Mona Allouba, Soha Romeih, Yasmine Aguib, A. John Baksi, Antonis Pantazis, Sanjay K. Prasad, Elisabetta Cerbai, Magdi H. Yacoub, Declan P. O’Regan, Stuart A. Cook, James S. Ware, Birgit Funke, Iacopo Olivotto, Connie R. Bezzina, Paul J. R. Barton, Roddy Walsh
Genet Med. 2021; 23(5): 856–864. Published online 2021 Jan 26. doi: 10.1038/s41436-020-01049-x
PMCID:
PMC8105165
ArticlePubReaderPDF–918KCite
7.
Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional Deficits
James G.W. Smith, Thomas Owen, Jamie R. Bhagwan, Diogo Mosqueira, Elizabeth Scott, Ingra Mannhardt, Asha Patel, Roberto Barriales-Villa, Lorenzo Monserrat, Arne Hansen, Thomas Eschenhagen, Sian E. Harding, Steve Marston, Chris Denning
Stem Cell Reports. 2018 Nov 13; 11(5): 1226–1243. Published online 2018 Nov 1. doi: 10.1016/j.stemcr.2018.10.006
PMCID:
PMC6235010
ArticlePubReaderPDF–4.6MCite
8.
Semi-automatic detection of myocardial trabeculation using cardiovascular magnetic resonance: correlation with histology and reproducibility in a mouse model of non-compaction
Julien Frandon, Stéphanie Bricq, Zakarya Bentatou, Laetitia Marcadet, Pierre Antoine Barral, Mathieu Finas, Daniel Fagret, Frank Kober, Gilbert Habib, Monique Bernard, Alain Lalande, Lucile Miquerol, Alexis Jacquier
J Cardiovasc Magn Reson. 2018; 20: 70. Published online 2018 Oct 25. doi: 10.1186/s12968-018-0489-0
PMCID:
PMC6201553
ArticlePubReaderPDF–2.0MCite
9.
Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies
Chaoxia Lu, Wei Wu, Fang Liu, Kunqi Yang, Jiacheng Li, Yaping Liu, Rongrong Wang, Nuo Si, Peng Gao, Yongtai Liu, Shuyang Zhang, Xue Zhang
J Transl Med. 2018; 16: 241. Published online 2018 Aug 30. doi: 10.1186/s12967-018-1605-5
PMCID:
PMC6117967
ArticlePubReaderPDF–842KCite
10.
Potential common pathogenic pathways for the left ventricular noncompaction cardiomyopathy (LVNC)
Ying Liu, Hanying Chen, Weinian Shou
Pediatr Cardiol. Author manuscript; available in PMC 2019 Aug 1.
Published in final edited form as: Pediatr Cardiol. 2018 Aug; 39(6): 1099–1106. Published online 2018 May 15. doi: 10.1007/s00246-018-1882-z
PMCID:
PMC6093786
ArticlePubReaderPDF–1.0MCite
11.
A Wide and Specific Spectrum of Genetic Variants and Genotype–Phenotype Correlations Revealed by Next‐Generation Sequencing in Patients with Left Ventricular Noncompaction
Ce Wang, Yukiko Hata, Keiichi Hirono, Asami Takasaki, Sayaka Watanabe Ozawa, Hideyuki Nakaoka, Kazuyoshi Saito, Nariaki Miyao, Mako Okabe, Keijiro Ibuki, Naoki Nishida, Hideki Origasa, Xianyi Yu, Neil E. Bowles, Fukiko Ichida, for LVNC Study Collaborators
J Am Heart Assoc. 2017 Sep; 6(9): e006210. Published online 2017 Aug 30. doi: 10.1161/JAHA.117.006210
PMCID:
PMC5634278
ArticlePubReaderPDF–1.4MCite
12.
Naturally Occurring Biventricular Noncompaction in an Adult Domestic Cat
M.D. Kittleson, P.R. Fox, C. Basso, G. Thiene
J Vet Intern Med. 2017 Mar-Apr; 31(2): 527–531. Published online 2017 Feb 3. doi: 10.1111/jvim.14663
PMCID:
PMC5354045
ArticlePubReaderPDF–1.3MCite
13.
Electrocardiographic findings in correlation to magnetic resonance imaging patterns in African patients with isolated ventricular noncompaction
Salwa Akhbour, Ibtissam Fellat, Nada Fennich, Salima Abdelali, Nawal Doghmi, Fedoua Ellouali, Mohammed Cherti
Anatol J Cardiol. 2015 Jul; 15(7): 550–555. Published online 2014 Jul 11. doi: 10.5152/akd.2014.5577
PMCID:
PMC5337034
ArticlePubReaderPDF–86KCite
14.
Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort
Jian Wang, Ying Guo, Meirong Huang, Zhen Zhang, Junxue Zhu, Tingliang Liu, Lin Shi, Fen Li, Huimin Huang, Lijun Fu
Orphanet J Rare Dis. 2017; 12: 26. Published online 2017 Feb 10. doi: 10.1186/s13023-016-0562-4
PMCID:
PMC5301434
ArticlePubReaderPDF–1.6MCite
15.
Cardiomyopathy Phenotypes and Outcomes for Children with Left Ventricular Myocardial Noncompaction: Results from the Pediatric Cardiomyopathy Registry
John L. Jefferies, James D. Wilkinson, Lynn A. Sleeper, Steven D. Colan, Minmin Lu, Elfriede Pahl, Paul F. Kantor, Melanie D. Everitt, Steven A. Webber, Beth D. Kaufman, Jacqueline M. Lamour, Charles E. Canter, Daphne T. Hsu, Linda J. Addonizio, Steven E. Lipshultz, Jeffrey A. Towbin, the Pediatric Cardiomyopathy Registry Investigators
J Card Fail. Author manuscript; available in PMC 2016 Nov 1.
Published in final edited form as: J Card Fail. 2015 Nov; 21(11): 877–884. Published online 2015 Jul 9. doi: 10.1016/j.cardfail.2015.06.381
PMCID:
PMC4630116
ArticlePubReaderPDF–1.5MCite
16.
Ensemble Force Changes that Result from Human Cardiac Myosin Mutations and a Small-Molecule Effector
Tural Aksel, Elizabeth Choe Yu, Shirley Sutton, Kathleen M. Ruppel, James A. Spudich
Cell Rep. Author manuscript; available in PMC 2016 May 12.
Published in final edited form as: Cell Rep. 2015 May 12; 11(6): 910–920. Published online 2015 Apr 30. doi: 10.1016/j.celrep.2015.04.006
PMCID:
PMC4431957
ArticlePubReaderPDF–2.4MCite
17.
Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death
Richard D Bagnall, Laura K Molloy, Jonathan M Kalman, Christopher Semsarian
BMC Med Genet. 2014; 15: 99. Published online 2014 Sep 16. doi: 10.1186/s12881-014-0099-0
PMCID:
PMC4355500
ArticlePubReaderPDF–1.8MCite
18.
Interpreting Secondary Cardiac Disease Variants in an Exome Cohort
David Ng, Jennifer J. Johnston, Jamie K. Teer, Larry N. Singh, Lindsey C. Peller, Jamila S. Wynter, Katie L. Lewis, David N. Cooper, Peter D. Stenson, James C. Mullikin, Leslie G. Biesecker
Circ Cardiovasc Genet. Author manuscript; available in PMC 2014 Aug 1.
Published in final edited form as: Circ Cardiovasc Genet. 2013 Aug; 6(4): 10.1161/CIRCGENETICS.113.000039. Published online 2013 Jul 16. doi: 10.1161/CIRCGENETICS.113.000039
PMCID:
PMC3887521
ArticlePubReaderPDF–760KCite
19.
Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy
Anne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, M. Khaled Sabeh, Eva R. Plovie, Almuth Caliebe, Eva Klopocki, Gabriel Musso, Andreas A. Werdich, Hermann Kalwa, Matthias Heinig, Robert F. Padera, Katharina Wassilew, Julia Bluhm, Christine Harnack, Janine Martitz, Paul J. Barton, Matthias Greutmann, Felix Berger, Norbert Hubner, Reiner Siebert, Hans-Heiner Kramer, Stuart A. Cook, Calum A. MacRae, Sabine Klaassen
Am J Hum Genet. 2013 Jul 11; 93(1): 67–77. doi: 10.1016/j.ajhg.2013.05.015
PMCID:
PMC3710750
ArticlePubReaderPDF–2.6MCite
20.
Monoamniotic Monochorionic Twins Discordant for Noncompaction Cardiomyopathy
Dianna Ng, Yosr Bouhlal, Philip C. Ursell, Joseph T.C. Shieh
Am J Med Genet A. Author manuscript; available in PMC 2014 Jun 1.
Published in final edited form as: Am J Med Genet A. 2013 Jun; 161(6): 1339–1344. Published online 2013 May 1. doi: 10.1002/ajmg.a.35925
PMCID:
PMC3664136
ArticlePubReaderPDF–1.4MCite

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