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Developmental Neuroscience|September 1, 2021
Nonsyndromic Early-Onset Epileptic Encephalopathies: Two Novel KCTD7 Pathogenic Variants and a Literature ReviewSima Binaafar, Masoud Garshasbi, Ali Reza Tavasoli, et al.
Cardiovascular Toxicology|May 20, 2018
Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary InterventionNejat Mahdieh, Ahmad Rabbani, Ata Firouzi, et al.
Genetic Testing and Molecular Biomarkers|March 11, 2011
Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variantNejat Mahdieh, Bahareh Rabbani, Atefeh Shirkavand, et al.
Cardiovascular Toxicology|August 11, 2018
Correction to: Clopidogrel Pharmacogenetics in Iranian Patients Undergoing Percutaneous Coronary InterventionNejat Mahdieh, Ahmad Rabbani, Ata Firouzi, et al.
Genetic Testing and Molecular Biomarkers|October 25, 2011
Mutation analysis of the CYP21A2 gene in the Iranian populationBahareh Rabbani, Nejat Mahdieh, Mohammad Tahgi Haghi Ashtiani, et al.
Journal of Tropical Pediatrics|September 9, 2008
Vitamin D insufficiency among children and adolescents living in Tehran, IranAli Rabbani, Seyed-Moayed Alavian, Mohammad Esmaeil Motlagh, et al.
Brain & Development|December 21, 2023
A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophiesSareh Hosseinpour, Ehsan Razmara, Morteza Heidari, et al.
Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
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