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Cell Journal|June 19, 2019
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital AnomaliesAkbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, et al.
Cerebellum (London, England)|June 22, 2022
Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging SpectraMahmoud Reza Ashrafi, Pouria Mohammadi, Ali Reza Tavasoli, et al.
Stem Cell Research & Therapy|August 7, 2021
Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trialMan Amanat, Anahita Majmaa, Morteza Zarrabi, et al.
Scientific Reports|May 19, 2026
Impact of stem cell therapy on brain metabolic profile in cerebral palsy assessed by magnetic resonance spectroscopy in a randomized clinical trialMelika Jameie, Neda Pak, Mehrdad Mozafar, et al.
Iranian Journal of Allergy, Asthma, and Immunology|May 11, 2026
The Value of Anti-Drug Antibody Detection in Discriminating Patients from Healthy Controls and Predicting the Gross Motor Functional State in Patients with Pompe DiseaseSolmaz Aziz-Ahari, Mahdi Aminian, Aliasghar Rahimian, et al.
Archives of Iranian Medicine|August 6, 2023
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based StudyElmira Haji Esmaeil Memar, Morteza Heidari, Homa Ghabeli, et al.
Epilepsy Research|July 6, 2026
Genetic heterogeneity, movement disorders, and white matter abnormalities in pediatric developmental and epileptic encephalopathies: A retrospective cohort study from a National Neurodegenerative and Leukodystrophy RegistryPouria Mohammadi, Sahand Fateh Tehrani, Reza Shervin Badv, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2022
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalitiesElla F Whittle, Madison Chilian, Ehsan Ghayoor Karimiani, 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.
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.
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