Results 271 to 280 of about 125,690 (294)

Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease

Huzairi Sani, Lay Kek Teh, Mohd Nur Fakhruzzaman Noorizhab, Norzuliana Zainal Abidin, Umi Nabila Mat Yusuf, Nada Syazana Zulkufli, Sazzli Kasim, Mohd Zaki Salleh   +7 more
openalex   +1 more source

Malignant Anomalous Aortic Origin of the Left Main Coronary Artery Managed by Ostial Reimplantation: A Case Report

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Anomalous origin of the left main coronary artery (LMCA) from the right coronary sinus with an interarterial course is a rare congenital variant associated with a high risk of myocardial ischemia and sudden cardiac death. We describe a 39‐year‐old man presenting with exertional chest pressure and dyspnea whose coronary CT angiography revealed ...
Biruk T. Mengistie, Chernet T. Mengistie, Asteway M. Haile, Nahom D. Gerer, Samuel Mesfin Girma, Elezer B. Zewde   +5 more
wiley   +1 more source

Validation of the HCM Risk-SCD Model in a Chinese Hypertrophic Cardiomyopathy Cohort. [PDF]

J Clin Med
Hang F, Fan C.
europepmc   +1 more source

Molecular genetic characteristics of patients with hypertrophic cardiomyopathy: a review

Yu. A. Yus'kiv, А. А. Чернова, S. Yu. Nikulinа, D. B. Drobot, V. A. Sakovich, O. O. Kardashova   +5 more
openalex   +1 more source

A Middle‐Aged Man With Pulseless VT and Dual Pathology: Anomalous Left Main Coronary Artery From Right Coronary Cusp With Transseptal Course and Underlying Dilated Cardiomyopathy

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Anomalous aortic origin of a coronary artery from the opposite sinus (AOCAOS) is a rare variety of coronary artery anomalies. Left main coronary artery (LMCA) arising from right coronary cusp (RCC) with a transseptal course is an uncommon variant that may not be as benign as previously thought.
Amir Heidari, Enssieh Hashemi, Mehrdad Jafari Fesharaki, Golnaz Houshmand, Roghaye Ghiasvand‐Mohammadkhani   +4 more
wiley   +1 more source

Comprehensive Review: Mavacamten and Aficamten in Hypertrophic Cardiomyopathy. [PDF]

Biomedicines
Savsin H, Tokarek T.
europepmc   +1 more source

Anesthetic Management for Pituitary Tumor Resection in a Patient With Acromegalic Cardiomyopathy: A Case Report

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Acromegalic cardiomyopathy is one of the common comorbidities of cardiovascular diseases in patients with acromegaly, and it is also a major risk factor affecting the survival rate of patients with acromegaly. The perioperative management of such patients is a challenge for anesthesiologists.
Shuting Yang, Mi Wang
wiley   +1 more source

Myosin inhibitors for treatment of hypertrophic cardiomyopathy. [PDF]

Cochrane Database Syst Rev
Quill S, Amin AS, Asselbergs FW, Bezzina C, Elliott PM, van der Velden J, Schmidt AF.   +6 more
europepmc   +1 more source

Safe General Anesthesia in a Pediatric Patient With 1p36.33 Duplication Syndrome: A Rare Case Report

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT 1p36.33 Duplication Syndrome is an extremely rare autosomal dominant multi‐gene disorder, including the disruption of the ATAD3 gene cluster, which encodes for mitochondrial membrane proteins. As of 2025, there is only one publicly available article highlighting the characteristic findings in patients with this condition; however, there is no ...
Michael McNally, Esha Thakkar, Adrienne Hutton   +2 more
wiley   +1 more source

Relationship between genotype and clinical phenotype of hypertrophic cardiomyopathy. [PDF]

World J Cardiol
Zhang LL, Wang B, Wang J, Zhao J, Liu LW.   +4 more
europepmc   +1 more source