Morteza Heidari

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 20

Top Venues

BMC pediatrics

Journal of molecular neuroscience : MN

Clinical case reports

Acta neurologica Belgica

Tehran University of Medical Sciences

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

Affiliation History

Tehran University of Medical Sciences

Iran

Assistant Professor :: Pediatric Neurology

Publications

Sareh Hosseinpour, Maryam Bemanalizadeh, Pouria Mohammadi, Mahmoud Reza Ashrafi, Morteza Heidari
An overview of early-onset cerebellar ataxia: a practical guideline. Acta neurologica Belgica (2024)
Elmira Hajiesmaeil Memar, Morteza Heidari, Homa Ghabeli, Elham Pourbakhtyaran, Roya Haghighi, Seyyed Mohammad Mahdi Hosseiny, Setareh Mamishi, Shima Mahmoudi, Hamid Eshaghi, Ali Reza Tavasoli, Mahmoud Mohammadi, Reza Shervin Badv, Gholamreza Zamani, Masood Ghahvehchi Akbari, Bahram Yarali, Rohola Shirzadi, Masoud Mohammadpour, Bahareh Yaghmaei, Meisam Sharifzadeh Ekbatani, Zeynab Najafi, Mahmoud Reza Ashrafi
Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study. Archives of Iranian medicine 26 (3) (2023)
Ali Najafi, Behnoosh Tasharrofi, Farshid Zandsalimi, Maryam Rasulinezhad, Masood Ghahvechi Akbari, Gholamreza Zamani, Mahmoud Reza Ashrafi, Morteza Heidari
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum. Italian journal of pediatrics 49 (1) (2023)
Seyedeh Atiyeh Afjei, Mohammad Farid Mohammadi, Elham Pourbakhtyaran, Homa Ghabeli, Mahmoud Reza Ashrafi, Roya Haghighi, Maryam Rasulinezhad, Neda Pak, Ali Reza Tavasoli, Morteza Heidari
Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT. Neurogenetics (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)
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)
Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari
Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy. BMC neurology 22 (1) (2022)
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
The quality of life in children with spinal muscular atrophy: a case-control study. BMC pediatrics 22 (1) (2022)
Elham Pourbakhtiaran, Morteza Heidari, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Gholamreza Zamani, Ali Reza Tavasoli, Zahra Rezaei, Setareh Mamishi, Elmira Haji Esmaeil Memar, Seyyed Mohammad Mahdi Hosseiny, Homa Ghabeli, Roya Haghighi, Mahmoud Reza Ashrafi
Childhood Guillain-Barre syndrome in the SARS-CoV-2 era: Is there any causative relation? Clinical case reports 10 (12) (2022)
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
The quality of life in children with spinal muscular atrophy: a case-control study. BMC pediatrics 22 (1) (2022)
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
The quality of life in children with spinal muscular atrophy: a case-control study. BMC pediatrics 22 (1) (2022)
Gholamreza Zamani, Mahmoud Reza Ashrafi, Homa Ghabeli, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Sareh Hosseinpour, Roya Haghighi, Elham Pourbakhtyaran, Nahid Khosroshahi, Morteza Heidari
The quality of life in children with spinal muscular atrophy: a case-control study. BMC pediatrics 22 (1) (2022)
Elham Pourbakhtiaran, Morteza Heidari, Masood Ghahvechi Akbari, Mahmoud Mohammadi, Reza Shervin Badv, Gholamreza Zamani, Ali Reza Tavasoli, Zahra Rezaei, Setareh Mamishi, Elmira Haji Esmaeil Memar, Seyyed Mohammad Mahdi Hosseiny, Homa Ghabeli, Roya Haghighi, Mahmoud Reza Ashrafi
Childhood Guillain-Barre syndrome in the SARS-CoV-2 era: Is there any causative relation? Clinical case reports 10 (12) (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)
Mahmoud Reza Ashrafi, Elham Pourbakhtyaran, Mohammad Rohani, Bita Shalbafan, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinezhad, Zahra Rezaei, Ali Zare Dehnavi, Seyyed Mohammad Mahdi Hosseiny, Roya Haghighi, Homa Ghabeli, Morteza Heidari
Follow-up of 25 patients with treatable ataxia: A comprehensive case series study. Clinical case reports 10 (4) (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)
Golnaz Ghazizadeh Esslami, Bahar Allahverdi, Reza Shervin Badv, Morteza Heidari, Nahid Khosroshahi, Hosein Shabani-Mirzaee, Kambiz Eftekhari
Clinical and Paraclinical Screening for Celiac Disease in Children with Intractable Epilepsy. Neurology research international 2021 (2021)
Gholamreza Zamani, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Sayna Bagheri, Kamyar Moradi, Mahmoud Reza Ashrafi, Ali Reza Tavasoli, Mahmoud Mohammadi, Reza Shervin Badv, Masood Ghahvechi Akbari, Morteza Heidari
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 : MN 70 (10) (2020)
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)

Top Topics

Top Venues

Morteza Heidari