Results 91 to 100 of about 222,830 (234)

Long-Term Outcomes of Hypertrophic Cardiomyopathy Diagnosed During Childhood: Results From a National Population-Based Study

Circulation, 2018
Background: Late survival and symptomatic status of children with hypertrophic cardiomyopathy have not been well defined. We examined long-term outcomes for pediatric hypertrophic cardiomyopathy.
P. Alexander, A. Nugent, P. Daubeney, Katherine J. Lee, L. Sleeper, T. Schuster, C. Turner, A. Davis, C. Semsarian, S. Colan, Terry Robertson, J. Ramsay, R. Justo, G. Sholler, I. King, R. Weintraub   +15 more
semanticscholar   +1 more source

HAeMODYNAMIC EFFECTS OF CHANGES IN BLOOD VOLUME IN HYPERTROPHIC OBSTRUCTIVE CARDIOMYOPATHY [PDF]

, 1965
Pravin M. Shah, R Amarasingham, C M Oakley   +2 more
openalex   +1 more source

A Deep Learning-Driven Pipeline for Differentiating Hypertrophic Cardiomyopathy from Cardiac Amyloidosis Using 2D Multi-View Echocardiography [PDF]

arXiv
Hypertrophic cardiomyopathy (HCM) and cardiac amyloidosis (CA) are both heart conditions that can progress to heart failure if untreated. They exhibit similar echocardiographic characteristics, often leading to diagnostic challenges. This paper introduces a novel multi-view deep learning approach that utilizes 2D echocardiography for differentiating ...
arxiv  

Beta-adrenergic Blockade in Hypertrophic Obstructive Cardiomyopathy [PDF]

, 1966
G Cherian, Ian Brockington, Pravin M. Shah, C M Oakley, J. F. Goodwin   +4 more
openalex   +1 more source

Clinical Profile and Consequences of Atrial Fibrillation in Hypertrophic Cardiomyopathy

Circulation, 2017
Background: Atrial fibrillation (AF), the most common sustained arrhythmia in hypertrophic cardiomyopathy (HCM), is capable of producing symptoms that impact quality of life and is associated with risk for embolic stroke.
E. Rowin, Anais Hausvater, M. Link, Patrick Abt, William J. Gionfriddo, Wendy Wang, H. Rastegar, N. Estes, M. Maron, B. Maron   +9 more
semanticscholar   +1 more source

Future Role of New Negative Inotropic Agents in the Era of Established Surgical Myectomy for Symptomatic Obstructive Hypertrophic Cardiomyopathy

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022
Barry J. Maron, Martin S. Maron, Mark V. Sherrid, Ethan J. Rowin   +3 more
doaj   +1 more source

Multi-Scale Fiber Remodeling in HCM Using a Stress-Based Fiber Reorientation Law [PDF]

arXiv
Quantifying fiber disarray, which is a prominent maladaptation associated with hypertrophic cardiomyopathy, remains critical to understanding the disease's complex pathophysiology. This study investigates the role of heterogeneous impairment of fiber contractility and fibrosis in the induction of disarray and their subsequent impact on cardiac pumping ...
arxiv  

Hypertrophic cardiomyopathy. [PDF]

, 1968
N. B. Karatzas, James Hamill, Peter Sleight   +2 more
openalex   +1 more source

Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy

Revista Portuguesa de Cardiologia, 2020
Introduction and objectives: Hypertrophic cardiomyopathy (HCM) is a genetically and phenotypically heterogeneous disease; there is still a large proportion of patients with no identified disease-causing mutation.
Alexandra Toste, Andreas Perrot, Cemil Özcelik, Nuno Cardim   +3 more
doaj  

Management of hypertrophic cardiomyopathy

Journal of Cardiovascular Medicine
Hypertrophic cardiomyopathy is an important cause of heart failure and arrhythmias, including sudden death, with a major impact on the healthcare system. Genetic causes and different phenotypes are now increasingly being identified for this condition.
Zhang, Yuhui, Adamo, Marianna, Zou, Changhong, Porcari, Aldostefano, Tomasoni, Daniela, Rossi, Maddalena, Merlo, Marco, Liu, Huihui, Wang, Jinxi, Zhou, Ping, Metra, Marco, Sinagra, Gianfranco, Zhang, Jian   +12 more
openaire   +4 more sources