Pouria Mohammadi
11PUBLICATIONS
14CO-AUTHORS
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Publications (11)
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|Feb 11, 2026
Super-Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review.Pouria Mohammadi, Lara Basovic, Christopher Michael McGraw
|Feb 20, 2025
Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating Leukodystrophy.Ali Reza Tavasoli, Arastoo Kaki, Maedeh Ganji
|Oct 26, 2023
Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers.Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani
|Jul 31, 2023
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature.Mohammad Farid Mohammadi, Ali Dehghani, Kiana Zarabadi
|Jun 22, 2022
Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.Mahmoud Reza Ashrafi, Pouria Mohammadi, Ali Reza Tavasoli
|Mar 11, 2022
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy.Mahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv
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Frequent Collaborators
6 joint publications
Morteza Heidari
5 joint publications
Masoud Garshasbi
3 joint publications
Nejat Mahdieh
2 joint publications
Mahmoud Reza Ashrafi
2 joint publications
Afshin Bahramy
2 joint publications
Ali Reza Tavasoli
1 joint publications
Mohammad Farid Mohammadi
1 joint publications
Ali Dehghani
1 joint publications
Kiana Zarabadi
1 joint publications
Seyyed Mohammad Kahani
