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Neuromolecular Medicine|July 2, 2024
A Comprehensive Overview of NF1 Mutations in Iranian PatientsShahram Savad, Mohammad-Hossein Modarressi, Sarang Younesi, 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.Molecular Genetics and Metabolism|June 18, 2026
Neuroradiological patterns and prognostic implications in type I Alexander diseaseYlenia Vaia, Filippo Arrigoni, Liat Ben Sira, et al.Clinical Genetics|September 3, 2025
Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype-Phenotype Correlations From 61 PatientsPegah Beheshti, Fahimeh Akbarian, Emran Esmaeilzadeh, et al.Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.Journal of Neuromuscular Diseases|February 19, 2025
Comparative efficacy of risdiplam and nusinersen in Type 2 and 3 spinal muscular atrophy patients: A cohort study using real-world dataMahmoud Reza Ashrafi, Marzieh Babaee, Seyed Saeed Hashemi Nazari, et al.Brain Communications|February 18, 2025
Biallelic <i>NDUFA13</i> variants lead to a neurodevelopmental phenotype with gradual neurological impairmentRauan Kaiyrzhanov, Kyle Thompson, Stephanie Efthymiou, et al.BMC Neurology|March 30, 2022
The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trialMorteza Zarrabi, Masood Ghahvechi Akbari, Man Amanat, et al.Journal of Neuromuscular Diseases|February 13, 2023
The First Report of Iranian Registry of Patients with Spinal Muscular AtrophyVahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, 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.Pageof 13