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Journal of Molecular Neuroscience : MN|May 22, 2020
The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense MutationsGholamreza Zamani, Ali Hosseini Bereshneh, Reza Azizi Malamiri, et al.Human Genomics|July 20, 2021
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variantsAli Zare Dehnavi, Erfan Heidari, Maryam Rasulinezhad, et al.BMC Immunology|July 27, 2025
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel casesErta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, et al.Journal of Child Neurology|March 12, 2020
Clinical Characteristics and Electrodiagnostic Features of Guillain-Barré Syndrome Among the Pediatric PopulationMahmoud Reza Ashrafi, Ariadokht Mohammadalipoor, Alireza Ranjbar Naeini, et al.Clinical Transplantation|June 13, 2025
Long-Term Outcomes of Hematopoietic Stem Cell Transplantation in Mucopolysaccharidoses Patients Without RadiationMohammad Jahanpanah, Leila Jafari, Maryam Behfar, et al.Journal of Child Neurology|January 16, 2018
The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry SystemMahmoud Reza Ashrafi, Zahra Rezaei, Morteza Heidari, et al.Clinical Case Reports|April 27, 2022
Follow-up of 25 patients with treatable ataxia: A comprehensive case series studyMahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, et al.Cephalalgia : an International Journal of Headache|June 4, 2019
Levetiracetam for prophylactic treatment of pediatric migraine: A randomized double-blind placebo-controlled trialHadi Montazerlotfelahi, Man Amanat, Ali Reza Tavasoli, et al.Journal of Molecular Neuroscience : MN|June 12, 2026
Exploratory Analysis of Neuroimaging and Molecular Findings in a Cohort of Neuronal Ceroid Lipofuscinosis: a Descriptive studyElham Rahimian, Majid R Tahsini, Mohadeseh Fathi, et al.Molecular Genetics and Metabolism|December 5, 2025
Genotype-phenotype correlations of GFAP variants in type I Alexander disease subtypesTiziana Bachetti, Ylenia Vaia, Alice Grossi, et al.Pageof 13