Pouria Mohammadi

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 9

Top Venues

Journal of molecular neuroscience : MN

Acta neurologica Belgica

Molecular genetics & genomic medicine

Cerebellum (London, England)

Hamadan University of Medical Sciences Medical School (MSC)

This page only lists publications with an associated author ORCID identifier.

Education History

Hamadan University of Medical Sciences Medical School Jul 16 2014

Iran

MSC

Publications

Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi
Expression assay of the COLQ in a family with congenital myasthenic syndrome and symptomatic carriers. Clinical case reports 11 (10) (2023)
Mohammad Farid Mohammadi, Ali Dehghani, Kiana Zarabadi, Seyyed Mohammad Kahani, Setareh Sayyad, Mahmoud Reza Ashrafi, Morteza Heidari, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature. Irish journal of medical science (2023)
Gholam Reza Zamani, Mohammad Farid Mohammadi, Ali Reza Tavasoli, Mahmoud Reza Ashrafi, Sareh Hosseinpour, Homa Ghabeli, Elham Pourbakhtyaran, Roya Haghighi, Seyyed Mohammad Mahdi Hosseiny, Pouria Mohammadi, Morteza Heidari
Genetic Analysis of Forty MLPA-Negative Duchenne Muscular Dystrophy Patients by Whole-Exome Sequencing. Journal of molecular neuroscience : MN 72 (5) (2022)
Mahmoud Reza Ashrafi, Pouria Mohammadi, Ali Reza Tavasoli, Morteza Heidari, Sareh Hosseinpour, Maryam Rasulinejad, Mohammad Rohani, Masoud Ghahvechi Akbari, Reza Azizi Malamiri, Reza Shervin Badv, Davood Fathi, Ali Zare Dehnavi, Shahram Savad, Ali Rabbani, Matthis Synofzik, Nejat Mahdieh, Zahra Rezaei
Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra. Cerebellum (London, England) (2022)
Ali Reza Tavasoli, Elmira Haji Esmaeil Memar, Mahmoud Reza Ashrafi, Seyed Mohammad Mahdi Hosseini, Roya Haghighi, Homa Ghabeli, Elham Pourbakhtyaran, Maryam Rasoulinezhad, Pouria Mohammadi, Morteza Heidari
Primary and Secondary Microcephaly, Global Developmental Delay, and Seizure in Two Siblings Caused by a Novel Missense Variant in the ZNF335 Gene. Journal of molecular neuroscience : MN 72 (4) (2022)
Mahmoud Reza Ashrafi, Roya Haghighi, Reza Shervin Badv, Homa Ghabeli, Ali Reza Tavasoli, Elham Pourbakhtyaran, Zahra Rezaei, Nejat Mahdieh, Pouria Mohammadi, Morteza Heidari
Epilepsia Partialis Continua a Clinical Feature of a Missense Variant in the ADCK3 Gene and Poor Response to Therapy. Journal of molecular neuroscience : MN 72 (5) (2022)
Pouria Mohammadi, Morteza Heidari, Mahmoud Reza Ashrafi, Nejat Mahdieh, Masoud Garshasbi
A novel homozygous missense variant in the NAXE gene in an Iranian family with progressive encephalopathy with brain edema and leukoencephalopathy. Acta neurologica Belgica (2021)
Pouria Mohammadi, Elham Salehi Siavashani, Mohammad Farid Mohammadi, Afshin Bahramy, Navid Almadani, Masoud Garshasbi
Whole-exome sequencing identified first homozygous frameshift variant in the COLEC10 gene in an Iranian patient causing 3MC syndrome type 3. Molecular genetics & genomic medicine 9 (11) (2021)
Pouria Mohammadi, Mohammad Ali Daneshmand, Nejat Mahdieh, Mahmoud Reza Ashrafi, Morteza Heidari, Masoud Garshasbi
Identification of a novel missense c.386G > A variant in a boy with the POMGNT1-related muscular dystrophy-dystroglycanopathy. Acta neurologica Belgica 121 (1) (2020)

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Publication Activity (10 Years)

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Pouria Mohammadi