Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Child Neurology|April 25, 2026
Seizure and Neurodevelopmental Regression in Inherited <i>N</i>-Acetyl Glutamate Synthase Deficiency (NAGSD): A Case Series From Neuroimaging to Genome SequencingAlireza Kooshki, Toktam Moosavian, Mahya Hosseini
Journal of Biomedical Materials Research. Part A|February 9, 2020
Electrically conductive materials for in vitro cardiac microtissue engineeringPayam Baei, Mahya Hosseini, Hossein Baharvand, et al.
Pediatric Gastroenterology, Hepatology & Nutrition|April 9, 2021
Vitamin D Effect on Ultrasonography and Laboratory Indices and Biochemical Indicators in the Blood: an Interventional Study on 12 to 18-Year-Old Children with Fatty LiverKokab Namakin, Mahya Hosseini, Mahmoud Zardast, et al.
Cell Journal|June 19, 2019
Iran's Contribution to Human Proteomic ResearchAnna Meyfour, Mahya Hosseini, Hamid Sobhanian, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 11, 2024
Galloway-mowat syndrome 3 (GAMOS3): a novel disease-causing variant in OSGEP gene and expansion of the clinical spectrumAbolfazl Yari, Farzane Vafaeie, Zahra Miri Karam, et al.
Daru : Journal of Faculty of Pharmacy, Tehran University of Medical Sciences|July 2, 2020
Cardenolide-rich fraction of Pergularia tomentosa as a novel Antiangiogenic agent mainly targeting endothelial cell migrationMahya Hosseini, Mahdi Ayyari, Anna Meyfour, et al.
Iranian Journal of Reproductive Medicine|February 6, 2015
Effect of prenatal methamphetamine administration during gestational days on miceArezoo Khoradmehr, Amirhossein Danafar, Iman Halvaei, et al.
Iranian Journal of Child Neurology|February 1, 2023
Clinical and MRI characteristics of multiple sclerosis in Iranian Children and AdolescentsMohammad Mahdi Nasehi, Ali Nikkhah, Sasan Saket, et al.
Neuromolecular Medicine|September 8, 2023
Identification of a Novel ARSA Gene Mutation Through High-Throughput Molecular Diagnosis Method in Two Girls with Late Infantile Metachromatic LeukodystrophyAbolfazl Yari, Farzane Vafaeie, Zahra Miri Karam, et al.
Cell Journal|June 29, 2026
Erratum : A Novel Insight into Endothelial and Cardiac Cells Phenotype in Systemic Sclerosis Using Patient-DerivedSedigheh Gholami, Zahra Mazidi, Sara Pahlavan, et al.
Pageof 2