Results 11 to 20 of about 311,439 (263)

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation [PDF]

, 2011
Genetic causes for autosomal recessive forms of dilated cardiomyopathy (DCM) are only rarely identified, although they are thought to contribute considerably to sudden cardiac death and heart failure, especially in young children.
Steenbergen, Gerry, van Reeuwijk, Jeroen, Lefeber, Dirk J, Kapusta, Livia, Wevers, Ron A, Zucker, Nili, Lammens, Martin, Absmanner, Birgit, Morava, Eva, van den Akker, Willem M R, Knopf, Carlos, Verrijp, Kiek, Grunewald, Stephanie, Schuurs-Hoeijmakers, Janneke H M, van Bokhoven, Hans, Jóźwiak, Adam, Lorber, Avraham, Riemersma, Moniek, Huijben, Karin, Lehle, Ludwig, Mandel, Hanna   +20 more
core   +4 more sources

A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers [PDF]

, 2011
Dilated cardiomyopathy (DCM) is a heterogeneous group of heart diseases with a strong genetic background. Currently, many human DCM cases exist where no causative mutation can be identified.
Matthew T. Webster, Gerhard Wess, Stephenson Hannah, Hannah Stephenson, Wess, G., Stephenson, Hannah, Cord Drögemüller, Webster, Matthew T., Mausberg, T.B., Webster, Matthew T.,, Webster, M.T., Dukes-McEwan, Joanna, Keller Lisa, Stephenson, H., Drögemüller, Michaela, Matthew T Webster, Leeb Tosso, Simak Julia, Droegemueller, Cord, Keller, L., Lisa Keller, Simak, J., Michaela Drögemüller, Simak, Julia, Dukes-McEwan, J., Joanna Dukes-McEwan, Tosso Leeb, Wess Gerhard, Mausberg, Theresa-Bernadette, Theresa-Bernadette Mausberg, Mausberg Theresa-Bernadette, Webster Matthew T., Droegemueller, Michaela, Wess, Gerhard, Drögemüller Cord, Drögemüller, Cord, Leeb, Tosso, Dukes-McEwan Joanna, Julia Simak, Drögemüller Michaela, Keller, Lisa, Stephenson H, Keller L, Mausberg TB, Dukes-McEwan J, Leeb T, Drögemüller M, Drögemüller C, Wess G, Webster MT, Simak J   +50 more
core   +2 more sources

Trans-Septal Myocardial Biopsy in Hypertrophic Cardiomyopathy Using the Liwen Procedure: An Introduction of a Novel Technique

Journal of Interventional Cardiology, 2021
Objective. The purpose of this study was to evaluate the feasibility and safety of myocardial biopsy using a new approach, the Liwen procedure. Background.
Chao Han, Mengyao Zhou, Rui Hu, Bo Wang, Lei Zuo, Jing Li, Shengjun Ta, David H. Hsi, Jiani Liu, Lichun Wei, Liwen Liu   +10 more
doaj   +1 more source

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry [PDF]

, 2023
Publisher Copyright: © The Author(s) 2022.Aims The interaction between common cardiovascular risk factors (CVRF) and hypertrophic cardiomyopathy (HCM) is poorly studied.
the Cardiomyopathy Registry Investigators Group
core   +1 more source

Analysis of desmoplakin in arrythmogenic right ventricular cardiomyopathy [PDF]

, 2010
Includes bibliographical references (leaves 71-79).It has been shown that all forms of cardiomyopathy, including the dilated, hypertrophic, restrictive, and right ventricular arrhythmogenic forms, are found in African populations.
Fish, Maryam
core   +1 more source

Hospital Procedural Volume and Clinical Outcomes Following Septal Reduction Therapy in Obstructive Hypertrophic Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2023
Background Prior national data showed a substantial in‐hospital mortality in septal myectomy (SM) with an inverse volume–outcomes relationship. This study sought to assess the contemporary outcomes of septal reduction therapy and volume–outcome ...
Ahmed M. Altibi, Fares Ghanem, Yuanzi Zhao, Miriam Elman, Joaquin Cigarroa, Babak Nazer, Howard K. Song, Ahmad Masri   +7 more
doaj   +1 more source

The role of melatonin in peripartum cardiomyopathy [PDF]

, 2013
Includes abstract.Includes bibliographical references.Peripartum cardiomyopathy (PPCM) is a heart disease of unknown aetiology emerging in previously healthy women towards the end of pregnancy or first postpartum months.
Nicholson, Lauren
core   +1 more source

Diffuse Fibrosis in Hypertrophic Cardiomyopathy

JACC: Advances
Background: Left ventricular (LV) myocardial extracellular volume (ECV), from cardiac magnetic resonance (CMR) T1 mapping, primarily reflects diffuse fibrosis and is a marker of adverse myocardial remodeling in hypertrophic cardiomyopathy (HCM ...
Susan K. Keen, MD, Hesham Sheashaa, MD, Stuti Shah, MD, Mohammed Abusafia, MD, Shada Jadam, MD, Simrat Kaur, MD, Andrew Gaballa, MD, Susan Ospina, NP, Katy Rutkowski, RN, Jay Ramchand, MD, PhD, Zoran B. Popovic, MD, PhD, Maran Thamilarasan, MD, Nicholas G. Smedira, MD, MBA, Paul Schoenhagen, MD, Michael Bolen, MD, Bo Xu, MD, Milind Y. Desai, MD, MBA   +16 more
doaj   +1 more source

Hypertrophic cardiomyopathy and ultra-endurance running - two incompatible entities? [PDF]

, 2011
Regular and prolonged exercise is associated with increased left ventricular wall thickness that can overlap with hypertrophic cardiomyopathy (HCM). Differentiating physiological from pathological hypertrophy has important implications, since HCM is the ...
Sanjay K Prasad, Papadakis, M, Sharma Sanjay, Prasad, Sanjay K., Chandra, N, Prasad, SK, O'Hanlon, Rory, O'Hanlon Rory, Papadakis, Michael, O'Hanlon, R, Chandra, Navin, Prasad Sanjay K, Michael Papadakis, Sharma, Sanjay, Chandra Navin, Papadakis Michael, Rory O'Hanlon, Wilson, MG, Wilson, Mathew G., Wilson Mathew G, Sanjay Sharma, Sharma, S, Mathew G Wilson, Navin Chandra   +23 more
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Differences in molecular phenotype in mouse and human hypertrophic cardiomyopathy

Scientific Reports, 2021
Hypertrophic cardiomyopathy (HCM) is characterized by phenotypic heterogeneity. We investigated the molecular basis of the cardiac phenotype in two mouse models at established disease stage (mouse-HCM), and human myectomy tissue (human-HCM).
Styliani Vakrou, Yamin Liu, Li Zhu, Gabriela V. Greenland, Bahadir Simsek, Virginia B. Hebl, Yufan Guan, Kirubel Woldemichael, Conover C. Talbot, Miguel A. Aon, Ryuya Fukunaga, M. Roselle Abraham   +11 more
doaj   +1 more source