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ARYA Atherosclerosis|March 28, 2015
A case of Marfan's syndrome with multi-level aortic dissectionsAlireza Khosravi, Mohaddeseh Behjati, Peyman Nilforoush, et al.
Environmental Science and Pollution Research International|July 27, 2020
CYP1A1 and GSTs common gene variations and presbycusis risk: a genetic association analysis and a bioinformatics approachMohammad Karimian, Mohaddeseh Behjati, Erfaneh Barati, et al.
Heart Failure Reviews|July 31, 2020
Cardiac complications in inherited mitochondrial diseasesMohaddeseh Behjati, Mohammad Reza Sabri, Masood Etemadi Far, et al.
The Annals of Thoracic Surgery|November 27, 2018
Isolated Congenital Dysgenesia of a Pulmonary Valve Cusp Presenting as a Pulmonary Artery AneurysmSedigheh Saedi, Kiara Rezaei-Kalantari, Mozhgan Parsaee, et al.
Echocardiography (Mount Kisco, N.Y.)|September 17, 2016
Cardiac computed tomography of an asymptomatic 48-year-old woman with ALCAPA syndromeAmirreza Sajjadieh Khajouei, Mohammadreza Samie-Nasab, Mohaddeseh Behjati, et al.
Advanced Biomedical Research|May 16, 2017
Evaluation of Energy Balance on Human Telomerase Reverse Transcriptase (hTERT) Alternative Splicing by Semi-quantitative RT-PCR in Human Umbilical Vein Endothelial CellsMohaddeseh Behjati, Mohammad Hashemi, Mohammad Kazemi, et al.
Journal of Cardiovascular and Thoracic Research|December 12, 2019
Prognostic value of normal and non-obstructive coronary artery disease based on CT angiography findings. A 12 month follow up studyAmirreza Sajjadieh Khajouei, Atoosa Adibi, Zahra Maghsodi, et al.
Bioinformation|May 4, 2012
Comparative modeling of CCRL1, a key protein in masked immune diseases and virtual screening for finding inhibitor of this proteinMohaddeseh Behjati, Ibrahim Torktaz, Mehrdad Mohammadpour, et al.
ARYA Atherosclerosis|October 12, 2012
Predictive value of P-wave duration and dispersion in post coronary artery bypass surgery atrial fibrillationMohammad Hashemi Jazi, Afshin Amirpour, Reihaneh Zavvar, et al.
BMC Medical Genomics|June 27, 2026
Identification of a novel pathogenic variant in MYLK in an Iranian family with non-syndromic familial aortic aneurysm and dissection by whole-exome sequencing and literature reviewHamide Jafari, Mansoor Salehi, Mohaddeseh Behjati, et al.
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