Results 201 to 210 of about 27,486 (234)

Characteristics, cost/effect consideration of clinical examinations, and construction of machine learning models of restrictive cardiomyopathy: insights from Peking Union Medical College Hospital. [PDF]

Int J Surg
Chen AT, Fang L, Lin X, Chen W.
europepmc   +1 more source

Heyde Syndrome: A Literature Review

Health Science Reports, Volume 9, Issue 2, February 2026.
ABSTRACT Background and Aims Heyde syndrome, a triad of anemia from gastrointestinal (GI) bleeding, aortic valve stenosis, and acquired von Willebrand syndrome, primarily affects individuals over 65. Management requires a multidisciplinary approach, including medical therapy, endoscopic intervention, and valve replacement.
Yashika Gupta, Abdul Rehman Shahid Khan, Viraj Shetty, Yeshwini Murali Krishna, Ayisha Maqsood, Muhammad Husnain Ahmad, Masab Ali, Betsy Samuel, Ali Gohar, Abdul Waheed, Muhammad Bilal Afzal, Rehan Naseer Ahmad, Saqib Maqsood   +12 more
wiley   +1 more source

Aborted sudden cardiac event in pediatric restrictive cardiomyopathy: When ST changes on ambulatory monitoring matter. [PDF]

HeartRhythm Case Rep
Christmas A, Nasman C, Boyle G, Patel A, Aziz P, El Assaad I.   +5 more
europepmc   +1 more source

Current Trends in Duchenne Muscular Dystrophy Research and Therapy: 3D Cardiac Modelling

Journal of Cachexia, Sarcopenia and Muscle, Volume 17, Issue 1, February 2026.
ABSTRACT Duchenne muscular dystrophy (DMD), caused by dystrophin deficiency, presents a multifaceted challenge that affects both skeletal muscle function and cardiomyocyte homeostasis, causing progressive degeneration and life‐threatening cardiac complications by adolescence.
Marta Przymuszała, Marta Białobrzeska, Józef Dulak, Urszula Florczyk‐Soluch   +3 more
wiley   +1 more source

Hypertrophic Cardiomyopathy Phenocopies: Classification, Key Features, and Differential Diagnosis. [PDF]

Biomedicines
Teresi L, Trimarchi G, Licordari R, Restelli D, Taverna G, Liotta P, Micari A, Smecca I, Dendramis G, Turturiello D, Latini AC, Falasconi G, de Gregorio C, Crea P, Dattilo G, Berruezo A, Micari A, Di Bella G.   +17 more
europepmc   +1 more source

Inherited cardiomyopathies: Contemporary genetics for clinical practice. [PDF]

Indian Pacing Electrophysiol J
Ahamed H, Hari A.
europepmc   +1 more source

A Genome‐Wide Association Study Reveals Desmoglein‐2 Predominance in Japanese Arrhythmogenic Cardiomyopathy

Journal of Arrhythmia, Volume 42, Issue 1, February 2026.
A GWAS of Japanese arrhythmogenic cardiomyopathy identified a strong signal near DSG2, exceeding the genome‐wide significance of p = 5 × 10–8 (red line). This signal disappeared after excluding carriers of rare DSG2 variants. Stratified analyses indicate that the association reflects a DSG2‐D494A‐mediated synthetic effect driven predominantly by this ...
Taisuke Ishikawa, Kyuto Sonehara, Keiko Sonoda, Kenshi Hayashi, Koichi Kato, Satoshi Nagase, Kengo Kusano, Takeshi Aiba, Minoru Horie, Seiko Ohno, Yukinori Okada, Naomasa Makita   +11 more
wiley   +1 more source

Clinical Outcomes of Patients Hospitalized for Conventional Pacemaker Implantation With Protein‐Energy Malnutrition

Journal of Arrhythmia, Volume 42, Issue 1, February 2026.
Protein‐energy malnutrition (PEM) was linked to higher in‐hospital mortality, longer hospital stays, and increased complications in patients undergoing pacemaker implantation. ABSTRACT Introduction The impact of protein‐energy malnutrition (PEM) on patients hospitalized for conventional pacemaker implantation remains poorly understood.
Phuuwadith Wattanachayakul, Pojsakorn Danpanichkul, Chalothorn Wannaphut, Hamza Tahir, John Malin, Thanathip Suenghataiphorn, Kanokphong Suparan, Aman Amanullah   +7 more
wiley   +1 more source

Primary prevention implantable cardioverter-defibrillator therapy in non-ischaemic heart failure with reduced left ventricular ejection fraction: a European Heart Rhythm Association survey. [PDF]

Europace
Brociek E, Karvonen J, Mills MT, Ruwald MH, Migliore F, Conte G, Roten L, Futyma P, Marcantoni L, Mazurek M, Sultan A, Duray GZ, Perrotta L, Chun JKR.   +13 more
europepmc   +1 more source

Cardiac dysfunction during adverse maternal outcomes in hypertensive disorders of pregnancy

Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 2, Page 280-287, February 2026.
In pregnancies complicated by hypertensive disorders, peripartum adverse maternal outcomes are associated with diastolic cardiac dysfunction. Elevated E/e' ratio and left atrial volume index highlight the need for targeted cardiovascular monitoring and long‐term follow‐up.
Veronica Giorgione, Jamie Kitt, Paul Leeson, Asma Khalil, Jamie O'Driscoll, Basky Thilaganathan   +5 more
wiley   +1 more source