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Items: 1 to 20 of 208

1.
Myocardial Effective Transverse Relaxation Time T2* is Elevated in Hypertrophic Cardiomyopathy: A 7.0 T Magnetic Resonance Imaging Study
Till Huelnhagen, Min-Chi Ku, Henning Matthias Reimann, Teresa Serradas Duarte, Andreas Pohlmann, Bert Flemming, Erdmann Seeliger, Christina Eichhorn, Victor A. Ferrari, Marcel Prothmann, Jeanette Schulz-Menger, Thoralf Niendorf
Sci Rep. 2018; 8: 3974. Published online 2018 Mar 5. doi: 10.1038/s41598-018-22439-x
PMCID:
PMC5838254
AbstractArticlePDF–3.2M
2.
High Spatial Resolution Cardiovascular Magnetic Resonance at 7.0 Tesla in Patients with Hypertrophic Cardiomyopathy – First Experiences: Lesson Learned from 7.0 Tesla
Marcel Prothmann, Florian von Knobelsdorff-Brenkenhoff, Agnieszka Töpper, Matthias A. Dieringer, Etham Shahid, Andreas Graessl, Jan Rieger, Darius Lysiak, C. Thalhammer, Till Huelnhagen, Peter Kellman, Thoralf Niendorf, Jeanette Schulz-Menger
PLoS One. 2016; 11(2): e0148066. Published online 2016 Feb 10. doi: 10.1371/journal.pone.0148066
PMCID:
PMC4749213
AbstractArticlePDF–3.2M
3.
Cardiac Function in 7-8-Year-Old Offspring of Women with Type 1 Diabetes
Maarten Rijpert, Johannes M. P. J. Breur, Inge M. Evers, Harold W. de Valk, Cobi J. Heijnen, Folkert J. Meijboom, Gerard H. A. Visser
Exp Diabetes Res. 2011; 2011: 564316. Published online 2011 Nov 15. doi: 10.1155/2011/564316
PMCID:
PMC3227501
AbstractArticlePDF–756K
4.
Parameters affecting outcome of paediatric cardiomyopathies in the intensive care unit: experience of an Egyptian tertiary centre over 7 years
Alaa A. Sobeih, Sonia A. El-Saiedi, Noha S. Abdel Khalek, Shereen A. Attia, Baher M. Hanna
Libyan J Med. 2020; 15(1): 1822073. Published online 2020 Oct 13. doi: 10.1080/19932820.2020.1822073
PMCID:
PMC7594879
AbstractArticlePDF–1.4M
5.
Sudden Cardiac Death Caused by a Fatal Association of Hypertrophic Cardiomyopathy (MYH7, p.Arg719Trp), Heterozygous Familial Hypercholesterolemia (LDLR, p.Gly343Lys) and SARS-CoV-2 B.1.1.7 Infection
Nicola Marziliano, Alessandro Medoro, Donatella Mignogna, Giovanni Saccon, Stefano Folzani, Claudio Reverberi, Claudio Russo, Mariano Intrieri
Diagnostics (Basel) 2021 Jul; 11(7): 1229. Published online 2021 Jul 7. doi: 10.3390/diagnostics11071229
PMCID:
PMC8307649
AbstractArticlePDF–1.6M
6.
A p.R870H mutation in the beta-cardiac myosin heavy chain 7 gene causes familial hypertrophic cardiomyopathy in several members of an Indian family
Murali D Bashyam, Gorinabele R Savithri, Munimanda Gopikrishna, Calambur Narasimhan
Can J Cardiol. 2007 Aug; 23(10): 788–790. doi: 10.1016/s0828-282x(07)70828-0
PMCID:
PMC2651383
AbstractArticlePDF–572K
7.
The clinical features, outcomes and genetic characteristics of hypertrophic cardiomyopathy patients with severe right ventricular hypertrophy
Xiying Guo, Chaomei Fan, Lei Tian, Yanling Liu, Hongyue Wang, Shihua Zhao, Fujian Duan, Xiuling Zhang, Xing Zhao, Fengqi Wang, Hongguang Zhu, Aiqing Lin, Xia Wu, Yishi Li
PLoS One. 2017; 12(3): e0174118. Published online 2017 Mar 21. doi: 10.1371/journal.pone.0174118
PMCID:
PMC5360271
AbstractArticlePDF–2.2M
8.
Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy
Hoshang Farhad, Sara B. Seidelmann, Davis Vigneault, Siddique A. Abbasi, Eunice Yang, Sharlene M. Day, Steven D. Colan, Mark W. Russell, Jeffrey Towbin, Mark V. Sherrid, Charles E. Canter, Ling Shi, Michael Jerosch-Herold, David A. Bluemke, Carolyn Ho, Tomas G. Neilan
J Cardiovasc Magn Reson. 2017; 19: 107. Published online 2017 Dec 28. doi: 10.1186/s12968-017-0420-0
PMCID:
PMC5745877
AbstractArticlePDF–1.0M
9.
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage
Shiv Kumar Viswanathan, Heather K. Sanders, James W. McNamara, Aravindakshan Jagadeesan, Arshad Jahangir, A. Jamil Tajik, Sakthivel Sadayappan
PLoS One. 2017; 12(11): e0187948. Published online 2017 Nov 9. doi: 10.1371/journal.pone.0187948
PMCID:
PMC5679632
AbstractArticlePDF–3.5M
10.
Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter
Alexander G. Bick, Hiroko Wakimoto, Kimberli J. Kamer, Yasemin Sancak, Olga Goldberger, Anna Axelsson, Daniel M. DeLaughter, Joshua M. Gorham, Vamsi K. Mootha, J. G. Seidman, Christine E. Seidman
Proc Natl Acad Sci U S A. 2017 Oct 24; 114(43): E9096–E9104. Published online 2017 Oct 9. doi: 10.1073/pnas.1711303114
PMCID:
PMC5664535
AbstractArticlePDF–1.0M
11.
The Burden of Early Phenotypes and the Impact of Left Ventricular Wall Thickness on Hypertrophic Cardiomyopathy Sarcomere Mutation Carriers: Findings from the HCMNet Study
Carolyn Y. Ho, Sharlene M. Day, Steven D. Colan, Mark W. Russell, Jeffrey Towbin, Mark V. Sherrid, Charles E. Canter, John Lynn Jefferies, Anne M. Murphy, Allison L. Cirino, Theodore P. Abraham, Matthew Taylor, Luisa Mestroni, David A. Bluemke, Petr Jarolim, Ling Shi, Lynn A. Sleeper, Christine E. Seidman, E. John Orav, for the HCMNet Investigators
JAMA Cardiol. Author manuscript; available in PMC 2018 Apr 1.
Published in final edited form as: JAMA Cardiol. 2017 Apr 1; 2(4): 419–428. doi: 10.1001/jamacardio.2016.5670
PMCID:
PMC5541992
AbstractArticlePDF–549K
12.
TRIM24 protein promotes and TRIM32 protein inhibits cardiomyocyte hypertrophy via regulation of dysbindin protein levels
Ankush Borlepawar, Ashraf Yusuf Rangrez, Alexander Bernt, Lynn Christen, Samuel Sossalla, Derk Frank, Norbert Frey
J Biol Chem. 2017 Jun 16; 292(24): 10180–10196. Published online 2017 May 2. doi: 10.1074/jbc.M116.752543
PMCID:
PMC5473223
AbstractArticlePDF–3.5M
13.
Pathogenesis of depression- and anxiety-like behavior in an animal model of hypertrophic cardiomyopathy
Amanda M. Dossat, Marcos A. Sanchez-Gonzalez, Andrew P. Koutnik, Stefano Leitner, Edda L. Ruiz, Brittany Griffin, Jens T. Rosenberg, Samuel C. Grant, Francis D. Fincham, Jose R. Pinto, Mohamed Kabbaj
FASEB J. 2017 Jun; 31(6): 2492–2506. Published online 2017 Feb 24. doi: 10.1096/fj.201600955RR
PMCID:
PMC5434648
AbstractArticle
14.
A Potential Oligogenic Etiology of Hypertrophic Cardiomyopathy, A Classic Single Gene Disorder
Lili Li, Matthew Neil Bainbridge, Yanli Tan, James T. Willerson, Ali J. Marian
Circ Res. Author manuscript; available in PMC 2018 Mar 31.
Published in final edited form as: Circ Res. 2017 Mar 31; 120(7): 1084–1090. Published online 2017 Feb 21. doi: 10.1161/CIRCRESAHA.116.310559
PMCID:
PMC5380229
AbstractArticlePDF–614K
15.
Assessment of regional left ventricular systolic function by strain imaging echocardiography in phenotypically normal and abnormal Maine coon cats tested for the A31P mutation in the MYBPC3 gene
Arine Pellegrino, Alexandre G.T. Daniel, Guilherme G. Pereira, Paula H. Itikawa, Maria Helena M.A. Larsson
Can J Vet Res. 2017 Apr; 81(2): 137–146.
PMCID:
PMC5370540
AbstractArticlePDF–1.1M
16.
Genetic basis of cardiomyopathy and the genotypes involved in prognosis and left ventricular reverse remodeling
Takashige Tobita, Seitaro Nomura, Takanori Fujita, Hiroyuki Morita, Yoshihiro Asano, Kenji Onoue, Masamichi Ito, Yasushi Imai, Atsushi Suzuki, Toshiyuki Ko, Masahiro Satoh, Kanna Fujita, Atsuhiko T Naito, Yoshiyuki Furutani, Haruhiro Toko, Mutsuo Harada, Eisuke Amiya, Masaru Hatano, Eiki Takimoto, Tsuyoshi Shiga, Toshio Nakanishi, Yasushi Sakata, Minoru Ono, Yoshihiko Saito, Seiji Takashima, Nobuhisa Hagiwara, Hiroyuki Aburatani, Issei Komuro
Sci Rep. 2018; 8: 1998. Published online 2018 Jan 31. doi: 10.1038/s41598-018-20114-9
PMCID:
PMC5792481
AbstractArticlePDF–2.5M
17.
Correlations between Endomyocardial Biopsies and Cardiac Manifestations in Taiwanese Patients with the Chinese Hotspot IVS4+919G>A Mutation: Data from the Fabry Outcome Survey
Ting-Rong Hsu, Fu-Pang Chang, Tzu-Hung Chu, Shih-Hsien Sung, Svetlana Bizjajeva, Wen-Chung Yu, Dau-Ming Niu
Int J Mol Sci. 2017 Jan; 18(1): 119. Published online 2017 Jan 9. doi: 10.3390/ijms18010119
PMCID:
PMC5297753
AbstractArticlePDF–3.6M
18.
Platelet Activation and Clopidogrel Effects on ADP‐Induced Platelet Activation in Cats with or without the A31P Mutation in MYBPC3
R.H.L. Li, J.A. Stern, V. Ho, F. Tablin, S.P. Harris
J Vet Intern Med. 2016 Sep-Oct; 30(5): 1619–1629. Published online 2016 Sep 12. doi: 10.1111/jvim.14568
PMCID:
PMC5032873
AbstractArticlePDF–651K
19.
Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy
Massimiliano Cecconi, Maria I. Parodi, Francesco Formisano, Paolo Spirito, Camillo Autore, Maria B. Musumeci, Stefano Favale, Cinzia Forleo, Claudio Rapezzi, Elena Biagini, Sabrina Davì, Elisabetta Canepa, Loredana Pennese, Mauro Castagnetta, Dario Degiorgio, Domenico A. Coviello, Collaborative Working Group
Int J Mol Med. 2016 Oct; 38(4): 1111–1124. Published online 2016 Sep 7. doi: 10.3892/ijmm.2016.2732
PMCID:
PMC5029966
AbstractArticlePDF–890K
20.
A Next-Generation Sequencing Approach to Identify Gene Mutations in Early- and Late-Onset Hypertrophic Cardiomyopathy Patients of an Italian Cohort
Speranza Rubattu, Cristina Bozzao, Ermelinda Pennacchini, Erika Pagannone, Beatrice Maria Musumeci, Maria Piane, Aldo Germani, Camilla Savio, Pietro Francia, Massimo Volpe, Camillo Autore, Luciana Chessa
Int J Mol Sci. 2016 Aug; 17(8): 1239. Published online 2016 Jul 30. doi: 10.3390/ijms17081239
PMCID:
PMC5000637
AbstractArticlePDF–229K

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