Results 201 to 210 of about 19,870 (257)

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

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

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

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

Two Cases of Post‐Operative Coronary–Cameral Fistulas After Unusual Myectomy Procedures

Clinical Case Reports, Volume 14, Issue 6, June 2026.
Post‐surgical coronary–cameral fistulas (CCF) can occur after various myectomy procedures. Here we present one case of CCF after resection of the hypertrophied RV muscle bundle in double‐chambered RV (DCRV) and one case of CCF after subaortic web resection.
Neda Toofaninejad, Arezoo Hajiali, Mahtab Hatami, Saba Mohammadzadeh   +3 more
wiley   +1 more source

NAT10‐mediated N4‐acetylcytidine modification drives RNA splicing of PML to alleviate adipose‐derived stem cell senescence and promote diabetic wound healing

Clinical and Translational Medicine, Volume 16, Issue 6, June 2026.
N‐acetyltransferase 10 (NAT10) catalyses N4‐acetylcytidine (ac4C) modification of PML pre‐mRNA, shifting splicing from the senescence‐promoting PML‐FL to the senescence‐inhibiting PML‐S isoform via SRSF1. This rejuvenates adipose‐derived stem cells (ADSCs) by reducing senescence markers and senescence‐associated secretory phenotype (SASP), thereby ...
Wuhan Wei, Chanyuan Jiang, Dong Zhu, Xuefeng Han, Xuan Ma, Xinyu Jia, Jiaqi Ling, Rui Zhang, Facheng Li, Ningbei Yin   +9 more
wiley   +1 more source

Beneficial effects of metoprolol in idiopathic dilated cardiomyopathy

, 1993
SINAGRA, GIANFRANCO, K. SWEDBERG, F. CAMERINI, A. DI LENARDA, G. LARDIERI, L. MESTRONI, M. R. BRISTOW, M. D'AVANZO, F. WAAGSTEIN, M. B. FOWLER FOR THE METROPROLOL IN DILATED CARDIOMYOPATHY MDC TRIAL STUDY GROUP IN ITALIA F. CAMERINI   +9 more
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Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

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Dilated Cardiomyopathy

Circulation Research, 2017
Dilated cardiomyopathy is defined by the presence of left ventricular dilatation and contractile dysfunction. Genetic mutations involving genes that encode cytoskeletal, sarcomere, and nuclear envelope proteins, among others, account for up to 35% of cases. Acquired causes include myocarditis and exposure to alcohol, drugs and toxins, and metabolic and
Elizabeth M Mcnally
exaly   +3 more sources