Results 131 to 140 of about 296,757 (381)

Diagnostic and prognostic value of low QRS voltages in cardiomyopathies: old but gold.

European Journal of Preventive Cardiology, 2020
The interpretation of 12-lead resting electrocardiogram (ECG) in patients with a definitive diagnosis or with the suspicion of a cardiomyopathy represents a cornerstone for the diagnostic work up and management of patients.
Francesca Valentini, F. Anselmi, M. Metra, L. Cavigli, E. Giacomin, M. Focardi, M. Cameli, S. Mondillo, F. D’Ascenzi   +8 more
semanticscholar   +1 more source

Cardiomyopathies and anaesthesia

Indian Journal of Anaesthesia, 2017
Cardiomyopathy is considered as a heart muscle disease of multiple aetiologies, unlike other cardiac diseases related to a definitive pathophysiology. With more and more research and with the advent of genetic analysis pin pointing the disease causing mutations, causative factors have been defined and classifications and definitions have changed over ...
Prajeesh M Nambiar, Rajiv Juneja
openaire   +3 more sources

Pancreatic Cancer‐Derived Extracellular Vesicles Enriched with miR‐223‐5p Promote Skeletal Muscle Wasting Associated with Cachexia

Advanced Science, EarlyView.
EVs and EV‐microRNAs (miRNAs) mediate PDAC‐skeletal muscle communication. miR‐223‐5p reduces METTL14 transcription by targeting MAFA, which subsequently decreases m6A methylation in skeletal muscles, ultimately leading to muscle wasting. This study highlights the absorption of miRNA in PDAC‐derived EVs by skeletal muscles and reveals a previously ...
Kangjing Xu, Rongxi Shen, Li Zhang, Xuejin Gao, Xinbo Wang, Changhua Zhang, Xi Chen, Xinying Wang   +7 more
wiley   +1 more source

Unraveling the genetic tapestry of pediatric sarcomeric cardiomyopathies and masquerading phenocopies in Jordan

Scientific Reports
Pediatric cardiomyopathies are mostly attributed to variants in sarcomere-related genes. Unfortunately, the genetic architecture of pediatric cardiomyopathies has never been previously studied in Jordan.
Bilal Azab, Dunia Aburizeg, Sherin T. Shaaban, Weizhen Ji, Lina Mustafa, Nooredeen Jamal Isbeih, Amal Saleh Al-Akily, Hashim Mohammad, Lauren Jeffries, Mustafa Khokha, Saquib A. Lakhani, Iyad Al-Ammouri   +11 more
doaj   +1 more source

Machine learning based classification and diagnosis of clinical cardiomyopathies.

Physiological Genomics, 2020
Dilated cardiomyopathy (DCM) and ischemic cardiomyopathy (ICM) are two common types of cardiomyopathies leading to heart failure. Accurate diagnostic classification of different types of cardiomyopathies is critical for precision medicine in clinical ...
A. Alimadadi, Ishan Manandhar, Sachin Aryal, P. Munroe, B. Joe, Xi Cheng   +5 more
semanticscholar   +1 more source

The challenge of cardiomyopathy

Journal of the American College of Cardiology, 1989
The combined clinical and pathophysiologic characteristics and diagnostic features as well as current concepts of pathogenesis, therapy and prevention of the principal forms of cardiomyopathy are reviewed. These include hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy and specific cardiac muscle disease.
Walter H. Abelmann, Beverly H. Lorell
openaire   +3 more sources

The Immune Microenvironment: New Therapeutic Implications in Organ Fibrosis

Advanced Science, EarlyView.
This review summarizes recent advances in understanding the immune microenvironment's role in fibrosis, focusing on phenotypic/functional alterations of immune cells and their dynamic interactions with other cellular constituents within tissues. The authors further explore therapeutic opportunities and challenges in targeting immune microenvironment ...
Xiangqi Chen, Chuan Wu, Fei Tang, Jingyue Zhou, Li Mo, Yanping Li, Jinhan He   +6 more
wiley   +1 more source

Personalized care in dilated cardiomyopathy: Rationale and study design of the activeDCM trial

ESC Heart Failure
Background Dilated cardiomyopathy (DCM) is a leading cause of heart failure, particularly in younger individuals. Low physical strength is a global risk factor for cardiovascular mortality, and physical activity and a healthy lifestyle have been shown to
Farbod Sedaghat‐Hamedani, Ali Amr, Theresa Betz, Elham Kayvanpour, Christoph Reich, Reto Wettstein, Oliver Heinze, Isabell Mohr, Regina Krisam, Anja Sander, Christina Klose, Birgit Friedmann‐Bette, Norbert Frey, Benjamin Meder   +13 more
doaj   +1 more source

Reversible cardiomyopathies

Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2018
Cardiac muscle dysfunction resulting in heart failure can be reversed with appropriate diagnosis and therapy in nearly 25%8211;50% of all nonischemic cardiomyopathies.
Anjaneyulu V Anne
doaj   +1 more source

Peripartum cardiomyopathy: diagnosis and management [PDF]

, 2017
No abstract ...
Coats, Caroline J., Dalzell, Jonathan R., Jackson, Alice M., Jhund, Pardeep S., Petrie, Mark C., Walker, Niki L.   +5 more
core   +1 more source