Results 191 to 200 of about 591,365 (304)

Emerging Upper Extremity Muscle Ultrasound Patterns as a Diagnostic Aid in TTN‐Related Myopathies

Muscle &Nerve, Volume 74, Issue 1, Page 111-120, July 2026.
ABSTRACT Introduction/Aims Biallelic pathogenic variants in TTN cause rare forms of early‐onset myopathy, manifesting with variable severity, distribution, and progression of muscle weakness, often associated with respiratory insufficiency and potentially cardiomyopathy. The large size of TTN and phenotypic heterogeneity in TTN‐related myopathy (TTN‐RM)
Abigail Potticary, Meghan McAnally, Sandra Donkervoort, Carsten G. Bönnemann   +3 more
wiley   +1 more source

Dilated Cardiomyopathy Phenotype With Global (Four-Chamber) Involvement in a Cat: Echocardiographic, Pathological, Histopathological, and Immunohistochemical Findings. [PDF]

Case Rep Vet Med
Romito G, Costa A, Morini M.
europepmc   +1 more source

Sustainable Low‐Field Cardiovascular Magnetic Resonance in Changing Healthcare Systems—An Update

NMR in Biomedicine, Volume 39, Issue 7, July 2026.
Low‐field cardiovascular MRI offers a cost‐effective and accessible alternative to conventional high‐field systems. Recent technological advances have improved image quality, safety, and device compatibility, expanding its clinical applications. These developments position low‐field CMR as a scalable solution to improve global cardiovascular imaging ...
Muhammad Umair, Ahmed Marey, Sanjana Murali, Udunna C. Anazodo, Adrienne E. Campbell‐Washburn, Ntobeko A. B. Ntusi, Orlando P. Simonetti, Thoralf Niendorf, Regina Mammen, Sola Adeleke   +9 more
wiley   +1 more source

AIDS and dilated cardiomyopathy [PDF]

Postgraduate Medical Journal, 1995
openaire   +2 more sources

Author Correction: Partial restoration of mitochondrial dysfunction by AAV-Ant1 protects from dilated cardiomyopathy in Ant1^-/- plus mtDNA mutant mice. [PDF]

Nat Commun
Angelin A, Keller K, Lu P, Guarnieri JW, Widjaja GA, Sule R, Janssen K, Olali A, Cen Z, Carosi V, Beauplan M, Murdock DG, Potluri P, Pei L, Wallace DC.   +14 more
europepmc   +1 more source

Pre‐Sport Cardiac Evaluation in Children: Detection of Risks Other Than Sudden Cardiac Death

Annals of Noninvasive Electrocardiology, Volume 31, Issue 4, July 2026.
In children who want to play sports, is a cardiac evaluation necessary only for sudden cardiac death? ABSTRACT Objective Sudden deaths may occur in children and adolescents due to unexpected cardiac problems during sports. This study aimed to screen for abnormalities that may lead to future morbidity in addition to the risk of sudden death and to ...
Mehmet Öncül, Abdulgani Gülyüz
wiley   +1 more source

Twenty-Five-Year Follow-Up of the MDDC1 Family: A <i>LMNA</i> Gene Variant Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement. [PDF]

Circ Genom Precis Med
Capovilla TM, Iseppi M, Distaso S, Gigli M, Dal Ferro M, Moretti M, Iorio A, Mancinelli A, Merlo M, Mestroni L, Paldino A, Sinagra G.   +11 more
europepmc   +1 more source

Causes of Persistent ST Elevation in Patients With Lung Cancer: A Case Report

Annals of Noninvasive Electrocardiology, Volume 31, Issue 4, July 2026.
ST elevation without Q waves in advanced cancer may suggest cardiac metastasis; voltage gradient while repolarization may cause ST elevation in cardiac metastasis. ABSTRACT Cardiac metastases are rare in clinical practice. Herein, we describe the case of a 61‐year‐old male patient who underwent radical left lung cancer surgery > 2 years before the ...
Lijiang Ding, Huayong Jin
wiley   +1 more source

Distinct CMR Phenotype in Alcoholic Cardiomyopathy: Greater Myocardial Fibrosis and Right Ventricular Dysfunction Compared with Idiopathic Dilated Cardiomyopathy. [PDF]

Diagnostics (Basel)
Vallejo-García V, Barreiro-Pérez M, González-Calle D, León Del Pino MDC, Jacas-Osborn V, Barrios C, Fabregat-Andrés Ó.   +6 more
europepmc   +1 more source

Autoantibodies in Patients With Arrhythmogenic Cardiomyopathy Activate GSK‐3β, Resulting in a Loss of Cardiomyocyte Cohesion

Acta Physiologica, Volume 242, Issue 7, July 2026.
ABSTRACT Background Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiac desmosome disease, as more than 50% of affected patients carry pathogenic variants in desmosome protein‐coding genes. In this study, we focused on the role and mechanisms of pathogenic and non‐pathogenic autoantibodies against intercalated disc (ICD) proteins such as ...
Soumyata Pathak, Konstanze Stangner, Ellen Kempf, Sina Moztarzadeh, Matthias Hiermaier, Stephanie Wider, Marlene Rauschmayer, Tatjana Williams, Andreas Stengl, Brenda Gerull, Ruth Biller, Sebastian Clauss, Stefan Kääb, Tomo Šarić, Sunil Yeruva, Jens Waschke   +15 more
wiley   +1 more source