Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the A Novel Homozygous Dph1 Mutation Causes Intellectual Disability and Unique Craniofacial Features
Mahmood Mohamadi
Mahmood Mohamadi

Professor of Pediatric Neurology

Department Pediatrics

School of Medicine

Childrens Medical Center

Tehran University of Medical Sciences

All Documents
1. An Efficient Approach for Detection of Various Epileptic Waves Having Diverse Forms in Long Term Eeg Based on Deep Learning, Brain Topography (2025)
2. Diversity in Clinical and Neurophysiological Manifestations of Epilepsy With Eyelid Myoclonia (Jeavons Syndrome) in Pediatric Population, Iranian Journal of Child Neurology (2025)
3. Learning Outcomes of Virtual Journal Clubs in Comparison to Real Ones in Pediatric Neurology Fellows, Iranian Journal of Child Neurology (2025)
4. Novel Co-Occurrence of Slc26a4 and Kctd7 Variants in a Pediatric Patient With Syndromic Hearing Loss and Myoclonic Epilepsy, Egyptian Journal of Medical Human Genetics (2025)
5. A Comparative Study on Prophylactic Efficacy of Cinnarizine and Amitriptyline in Childhood Migraine: A Randomized Double-Blind Clinical Trial, Cephalalgia (2024)
6. A Comprehensive Study of Mutation and Phenotypic Heterogeneity of Childhood Mitochondrial Leukodystrophies, Brain and Development (2024)
7. Effectiveness of Electronic Learning Courses on Neurologist Knowledge of Epilepsy Classification: A Study Based on the Kirkpatrick Model, Jundishapur Journal of Chronic Disease Care (2024)
8. Pcdh19-Clustering Epilepsy, Pathophysiology and Clinical Significance, Epilepsy and Behavior (2024)
9. The Value of Long-Term Video Eeg Monitoring to Diagnose and Track Childhood Epilepsy, Iranian Journal of Child Neurology (2024)
10. Comparing the Efficacy and Safety of Levetiracetam Versus Phenytoin for Treating the Acute Phase of Neonatal Seizures, Iranian Journal of Child Neurology (2023)
11. Correction To: High Genetic Heterogeneity of Leukodystrophies in Iranian Children: The First Report of Iranian Leukodystrophy Registry (Neurogenetics, (2023), 24, 4, (279-289), 10.1007/S10048-023-00730-Y), Neurogenetics (2023)
12. High Genetic Heterogeneity of Leukodystrophies in Iranian Children: The First Report of Iranian Leukodystrophy Registry, Neurogenetics (2023)
13. Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study, Archives of Iranian Medicine (2023)
14. Non-Invasive Electrical Source Imaging for Localizing Epileptiform Discharges in Children With Focal Epilepsy Based on Developing Country’S Limitations, Iranian Journal of Pediatrics (2023)
15. Normal Values of Nerve Conduction Studies in Children Aged 7 Days to 14 Years Referred to Electrodiagnosis Clinic of Iranian Children’S Medical Center, Iranian Journal of Pediatrics (2023)
16. Virtual and In-Person Electroencephalography (Eeg) Training Among Pediatric and Adult Neurology Residents During the Covid-19 Pandemic, Iranian Journal of Pediatrics (2023)
17. An Open-Label Phase 1 Clinical Trial of the Allogeneic Side Population Adipose-Derived Mesenchymal Stem Cells in Sma Type 1 Patients, Neurological Sciences (2022)
18. Characteristics of Disease Progression and Genetic Correlation in Ambulatory Iranian Boys With Duchenne Muscular Dystrophy, BMC Neurology (2022)
19. The Quality of Life in Children With Spinal Muscular Atrophy: A Case–Control Study, BMC Pediatrics (2022)
20. The Safety and Efficacy of Umbilical Cord Blood Mononuclear Cells in Individuals With Spastic Cerebral Palsy: A Randomized Double-Blind Sham-Controlled Clinical Trial, BMC Neurology (2022)
21. Cytomegalovirus Infection and Guillain-Barre Syndrome: The First Case-Control Study in Iran, Iranian Journal of Child Neurology (2021)
22. Clinical Characteristics and Electrodiagnostic Features of Guillain-Barre Syndrome Among the Pediatric Population, Journal of Child Neurology (2020)
23. Neonatal Seizure: How Reliable Is Its Diagnosis and Treatment? a Mini Review of Previous Knowledge, Iranian Journal of Child Neurology (2020)
24. The First Comprehensive Cohort of the Duchenne Muscular Dystrophy in Iranian Population: Mutation Spectrum of 314 Patients and Identifying Two Novel Nonsense Mutations, Journal of Molecular Neuroscience (2020)
25. We Need Well-Designed Multicenter Studies to Investigate Neurologic Manifestations of Coronavirus Disease 2019, Current Journal of Neurology (2020)
26. A Clinical Trial Evaluating the Safety and Efficiency of Cerebrolysin in Children With Autism Spectrum Disorders, Iranian Journal of Pediatrics (2019)
27. Hemi-Eses Associated With Agenesis of the Corpus Callosum and Normal Cognition, Epilepsy and Behavior Case Reports (2019)
28. Il-7Ra Association and Genotype-Dependent Severity and Response to Ifn-Β Therapy in Multiple Sclerosis, Acta Medica Iranica (2019)
29. Levetiracetam for Prophylactic Treatment of Pediatric Migraine: A Randomized Double-Blind Placebo-Controlled Trial, Cephalalgia (2019)
30. Overexpression of Smn2 Gene in Motoneuron-Like Cells Differentiated From Adipose-Derived Mesenchymal Stem Cells by Ponasterone A, Journal of Molecular Neuroscience (2019)
31. The First Report of Relative Incidence of Inherited White Matter Disorders in an Asian Country Based on an Iranian Bioregistry System, Journal of Child Neurology (2018)
32. The Efficacy of the Ketogenic Diet in Infants and Young Children With Refractory Epilepsies Using a Formula-Based Powder, Acta Neurologica Belgica (2017)
33. The Influence of Ketogenic Diet on Liver Function in Children and Adolescents With Intractable Epilepsy, Journal of Comprehensive Pediatrics (2017)
34. Association of Interleukin-1 Gene Cluster and Interleukin-1 Receptor Polymorphisms With Febrile Seizures, Journal of Child Neurology (2016)
35. The Effects of Classic Ketogenic Diet on Serum Lipid Profile in Children With Refractory Seizures, Acta Neurologica Belgica (2016)
36. The Quality of Life in Boys With Duchenne Muscular Dystrophy, Neuromuscular Disorders (2016)
37. Association of Il4 Single-Nucleotide Polymorphisms With Febrile Seizures, Journal of Child Neurology (2015)
38. Asymmetrical Generalized Paroxysmal Fast Activities in Children With Intractable Localization-Related Epilepsy, Brain and Development (2015)