Results 221 to 230 of about 591,365 (304)

Genotype-Phenotype Discordance in Cardiomyopathies: Pathophysiology, Clinical Expression, and Therapeutic Considerations. [PDF]

Health Sci Rep
Nazir A, Sarwar AH, Nazar R, Shahab SH, Manan S, Rafique H, Khan AT, Shubietah A, Zaidi SRH, Khan B.   +9 more
europepmc   +1 more source

Rate Versus Rhythm Control in a Multimorbid Patient With Tachy–Brady Syndrome: Evaluation of Clinical Outcomes and Pacing Dependency

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case report describes a 77‐year‐old man with multiple comorbidities, including atrial fibrillation, heart failure with mildly reduced ejection fraction, hypertension, diabetes mellitus, and prior coronary artery bypass grafting, who presented with severe hypertension and dyspnoea.
Reem Fakak, Emma Nordahl, Joseph Moutiris   +2 more
wiley   +1 more source

Decoding the Mitochondrial Translation-Stress Axis: Is TARS2 the Missing Link in DCM Pathogenesis? [PDF]

JACC Basic Transl Sci
Zeldin S, Sadoshima J.
europepmc   +1 more source

When Trabeculations Disrupt Conduction: Left Ventricular Noncompaction Presenting With Symptomatic Bradycardia and Isorhythmic Dissociation

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT In young patients with unexplained symptomatic bradycardia, LVNC should be considered even when initial echocardiography is equivocal. Precise ECG interpretation is essential—AV dissociation driven by a ventricular escape rhythm must be distinguished from true AV block, as this distinction directly determines whether cardiac MRI, genetic ...
Talha Shamshad, Ryan Salama, Jurgen Shtembari, Mounica Vorla, Muhammad Asif, Sanchit Duhan, Mohammad Al‐Akchar, Osama Alsara   +7 more
wiley   +1 more source

Digenic sarcomeric variants in paediatric dilated cardiomyopathy and maternal peripartum cardiomyopathy: a familial case report. [PDF]

Eur Heart J Case Rep
Kurt H, Ülger Tutar Z, Levent E, Karasulu Beci B, Doğan E.   +4 more
europepmc   +1 more source

Peripartum Cardiomyopathy Presenting With Severe Biventricular Dysfunction, Valvular Regurgitation, and Familial Predisposition: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Peripartum cardiomyopathy (PPCM) is defined as the onset of left ventricular systolic dysfunction either during pregnancy or up to 5 months after delivery, without any other known cause of heart failure. The exact pathogenesis of this disease is unknown, and its prognosis remains poorly understood.
Muhammad Ibrahim Shah, Hasnain Wajeeh Saqib, Maaz Khan, Muhammad Saeed Ullah Shah, Dadullah Faiz   +4 more
wiley   +1 more source

Occurrence of Left Ventricular Cavity Obliteration. [PDF]

Cureus
Tamilselvan K, Arumugam A, Vadivelu M.
europepmc   +1 more source

Atrial Flutter as a Late Presentation of Scimitar Vein in an Adult With Prior ASD Repair

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Adult patients with unexplained atrial arrhythmias and right heart dilation should prompt consideration of congenital anomalies such as scimitar vein, even decades after atrial septal defect repair. Early recognition using multi‐modality imaging may prevent delayed diagnosis and progressive cardiopulmonary complications.
Fereshte Rastegarnasab, Zahra Teimouri‐Jervekani, Keyvan Khojaste, Azam Soleimani   +3 more
wiley   +1 more source

Machine Learning in Nonischemic Cardiomyopathy: Phenotyping, Mechanism Discovery, and Clinical Applications. [PDF]

Cardiol Rev
Quansah K, Anderson E, Kwon E, Kwon C.
europepmc   +1 more source

Expanding the Phenotype of TAB2‐Related Syndrome: The First Case With Cleft Palate and Insights Into Palatal Development

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1427-1430, June 2026.
Alberto De Rosa, Silvia Kalantari, Marta Carboni, Antonella Casella, Elisa Giorgio, Antonia Apicella, Alessia Claudia Codazzi, Fabio Sirchia   +7 more
wiley   +1 more source