Results 81 to 90 of about 26,229 (182)

Clinical and genetic characterization of patients with hypertrophic cardiomyopathy and right atrial enlargement [PDF]

, 2016
AIMS: Prevalence and clinical significance of right atrial enlargement (RAE) has been poorly characterized in hypertrophic cardiomyopathy. METHODS: One hundred and sixty consecutive patients with hypertrophic cardiomyopathy (35.5 ± 20 years; 64% men ...
Bossone, E, Calabro, R, Elliott, P, Ferrara, I, Frisso, G, Gravino, R, Iacomino, M, Limongelli, G, Masarone, D, Pacileo, G, Rea, A, Salvatore, F   +11 more
core  

Dilated Cardiomyopathy With Mid‐Range Ejection Fraction at Diagnosis: Characterization and Natural History

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2019
Background Limited data are available on mid‐range ejection fraction (mrEF) patients with dilated cardiomyopathy. We sought to define the characteristics, evolution, and long‐term prognosis of dilated cardiomyopathy patients with mrEF at diagnosis ...
Piero Gentile, Marco Merlo, Antonio Cannatà, Marco Gobbo, Jessica Artico, Davide Stolfo, Marta Gigli, Federica Ramani, Giulia Barbati, Bruno Pinamonti, Gianfranco Sinagra   +10 more
doaj   +1 more source

A rare systemic etiology of heart failure and liver dysfunction

Clinical Case Reports, 2019
Systemic amyloidosis is a rare condition that can manifest with cardiomyopathy, hepatic dysfunction, and renal disease. Diagnosis is often missed and/or delayed due to chronic multi‐system involvement and indeterminate signs and symptoms.
Christopher Lee, Edward Chau, Sumit Patel, Diana Zhao, Alexander H. Yang, Brian T. Lee, Jacob Alexander, Enrique Ostrzega, Patrick Sarte   +8 more
doaj   +1 more source

An Unusual Case of 11αB‐Crystallin (CRYAB) Mutation as a Cause of Dilated Cardiomyopathy With Restrictive Physiology: A Case Report and Focused Review of the Literature

Clinical Case Reports
Several diseases have been linked to αB‐crystallin (CRYAB) mutation. However, this mutation is an uncommon cause that has been associated in recent years with the development of dilated cardiomyopathy.
Porras Bueno Cristian Orlando, Cruz Buitrago Roberto Hernando, Mariño Correa Alejandro, Cáceres Méndez Edward Andres, Eugenio Meek, Ríos Dueñas Edgar Giovanni   +5 more
doaj   +1 more source

CLINICAL FEATURES AND DIAGNOSTIC ALGORITHMS OF CARDIOMYOPATHIES WITH RESTRICTIVE PHENOTYPE CAUSED BY CARDIAC TROPONIN I AND DESMIN GENES MUTATIONS

Педиатрическая фармакология, 2011
The authors are citing the literature data and share their own experiences of observation of two patients with cardiomyopathy associated with restrictive phenotype caused by mutations in defined genes encoding the synthesis of cardiac troponin I and ...
M.V. Tural'chuk, G.A. Novik, A.Ya. Gudkova   +2 more
doaj   +2 more sources

Restrictive cardiomyopathy [PDF]

Postgraduate Medical Journal, 1986
openaire   +2 more sources

Comprehensive Strategies to Address Radiation-Induced Restrictive Cardiomyopathy

Cardiovascular Innovations and Applications
Radiation-induced cardiomyopathy has become a significant clinical challenge with the increased use of thoracic radiation therapy. Recent technological advancements in radiation therapy, such as 3D conformal radiation therapy (3D-CRT), intensity ...
Mohannad Al Akeel, Shahnawaz Notta, Ward Al Akeel, Laith Alhuneafat, Vijay Ramu, Manar Jbara   +5 more
doaj   +1 more source

Restrictive cardiomyopathy: Importance of early diagnosis

Anales de Pediatría (English Edition), 2021
Laia Brunet-Garcia, Ferran Roses-Noguer, Pedro Betrián, Joan Balcells, Ferran Gran   +4 more
doaj   +1 more source

Asymptomatic Hypertrophic Cardiomyopathy: Diagnosis and Therapy [PDF]

, 2017
Fuentes, V L, Wilkie, L J
core   +1 more source

Restrictive cardiomyopathy. [PDF]

Heart, 1990
P T, Wilmshurst, D, Katritsis
openaire   +4 more sources