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Scientific Reports|February 24, 2023
A comprehensive overview of SMN and NAIP copy numbers in Iranian SMA patientsShahram Savad, Mahmoud Reza Ashrafi, Niusha Samadaian, et al.
Clinical Case Reports|December 22, 2022
Childhood Guillain-Barre syndrome in the SARS-CoV-2 era: Is there any causative relation?Elham Pourbakhtyaran, Morteza Heidari, Masood Ghahvechi Akbari, et al.
Orphanet Journal of Rare Diseases|July 4, 2023
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patientsAli Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, 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.
Cephalalgia : an International Journal of Headache|April 20, 2024
A comparative study on prophylactic efficacy of cinnarizine and amitriptyline in childhood migraine: a randomized double-blind clinical trialMehrnaz Olfat, Sareh Hosseinpour, Safdar Masoumi, 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.
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.
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.
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