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Acta Cardiologica|March 18, 2025
Enhancing predictive accuracy of the 13-item Acute Coronary Syndrome checklist: a novel approach to improving risk assessment and diagnosisMohammad Sahebkar, Najme Lagzian, Mohammad Reza Armat, et al.
Stem Cell Research & Therapy|March 4, 2024
Evaluation of the efficacy of mesenchymal stem cells derived conditioned medium in the treatment of striae distensae: a double blind randomized clinical trialElham Behrangi, Masoomeh Feizollahi, Sona Zare, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 15, 2023
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infectionSahand Tehrani Fateh, Saman Bagheri, Hossein Sadeghi, et al.
Advances in Skin & Wound Care|October 6, 2020
Evaluation of Dried Amniotic Membrane on Wound Healing at Split-Thickness Skin Graft Donor Sites: A Randomized, Placebo-Controlled, Double-blind TrialMojtaba Vaheb, Bahareh Mohajer Kohestani, Maryam Karrabi, et al.
Iranian Journal of Neurology|July 19, 2017
Multiple sclerosis-A disease on a dramatically rising trend in Iran: Review of possible reasonsMohammad Ali Sahraian, Mohammad Sahebkar, Rouhullah Dehghani, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|December 4, 2024
Effect of low-frequency blood glucose self-monitoring on glycosylated hemoglobin levels among older adults with type 2 diabetes mellitusMohammad Sahebkar, Atousa Ariafar, Farnush Attarzadeh, et al.
Geriatrics & Gerontology International|June 23, 2022
Evaluating the effects of telenursing on patients' activities of daily living and instrumental activities of daily living after myocardial infarction: A randomized controlled trial studyNarges Sefidi, Abdolghader Assarroudi, Zahra Zandi, et al.
Molecular Genetics & Genomic Medicine|January 21, 2025
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel VariantMohammad-Reza Ghasemi, Zahra Esmaeilizadeh, Sahand Tehrani Fateh, et al.
Biochemical Genetics|April 19, 2025
Exome Sequencing in 9 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet-Biedl SyndromeMohammad Reza Seyedtaghia, Mohsen Habibi, Farzad Hashemi-Gorji, et al.
Journal of Nursing Care Quality|June 23, 2020
Evaluation of the Impact of Handoff Based on the SBAR Technique on Quality of Nursing CareAli Abbaszade, Abdolghader Assarroudi, Mohammad Reza Armat, et al.
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