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ESC Heart Failure|February 8, 2024
A novel likely pathogenic homozygous RBCK1 variant in dilated cardiomyopathy with muscle weaknessMohammadHossein MozafaryBazargany, Shiva Esmaeili, Mahshid Hesami, et al.Clinical Case Reports|July 28, 2022
Multimodality imaging in the diagnostic approach to a patient with carcinoid heart disease involving four heart valvesShirin Habibi Khorasani, Mozhgan Parsaee, Niloufar Samiei, et al.Health Science Reports|January 8, 2024
Role of feature tracking cardiac magnetic resonance imaging in early detection of cardiac dysfunction in β-thalassemia patients recovered from COVID-19: A cross-sectional studyGolnaz Houshmand, Mozhgan Parsaee, Leila Najmafshar, et al.Cardiology Research and Practice|July 13, 2026
Evaluation of Aortic Dilation in Patients With Hypertrophic Cardiomyopathy in a Tertiary Center for Cardiovascular DiseaseTahereh Babaei, Kosar Babaei, Golnaz Houshmand, et al.Journal of Digital Imaging|September 22, 2023
Left Ventricular Myocardial Dysfunction Evaluation in Thalassemia Patients Using Echocardiographic Radiomic Features and Machine Learning AlgorithmsHaniyeh Taleie, Ghasem Hajianfar, Maziar Sabouri, et al.Cardiology Research and Practice|January 16, 2025
Comparison of Cardiac Magnetic Resonance Imaging Findings and Prognostic Measures in Nondilated Cardiomyopathy and Dilated CardiomyopathyAli Asghari, Golnaz Houshmand, Mohammad Javad Aminizadeh, et al.Journal of Cardiovascular and Thoracic Research|November 29, 2023
Polymorphism of rs599839 in the <i>PSRC1</i> gene is associated with coronary artery disease in an Iranian populationGolnaz Houshmand, Mohammad Javad Alemzadeh-Ansari, Saeideh Mazloumzadeh, et al.BMC Musculoskeletal Disorders|March 28, 2024
A novel homozygous variant (c.5876T > C: p. Leu1959Pro) in DYSF segregates with limb-girdle muscular dystrophy: a case reportHamed Hesami, Serwa Ghasemi, Golnaz Houshmand, et al.Heart Failure Reviews|May 16, 2023
Feature tracking cardiac magnetic resonance imaging to assess cardiac manifestations of systemic diseasesParmida Sadat Pezeshki, Seyyed Mojtaba Ghorashi, Golnaz Houshmand, et al.BMC Medical Genomics|March 7, 2025
Unraveling a novel FBN1 variant in Marfan syndrome with dilated aortic root manifestationAmirreza Sabahizadeh, Amir Askarinejad, Saranaz Seyed AliAkbar, et al.Pageof 4