Ali Reza Tavasoli

ResearcherID Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 24

Top Venues

AJNR. American journal of neuroradiology

Orphanet journal of rare diseases

Neurogenetics

Acta neurologica Belgica

Tehran University of Medical Sciences School of Pharmacy

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

Affiliation History

Tehran University of Medical Sciences School of Pharmacy Dec 22 2012

Iran

Attending physician/Research physician :: Neurology

Publications

Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Maedeh Ganji, Pouria Mohammadi, Tayyeb Bahrami, Mahmoud Reza Ashrafi, Sareh Hosseinpour, Morteza Heidari, Masoud Garshasbi, Ali Reza Tavasoli
Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant. Acta neurologica Belgica (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli, Arastoo Vossough, Mariko L Bennett, Ylenia Vaia, Geneviève Bernard, Ettore Salsano, Saadet Mercimek-Andrews, Amy Waldman, Adeline Vanderver
Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. AJNR. American journal of neuroradiology 45 (6) (2024)
Narges Hashemi, Reza Nejad Shahrokh Abadi, Afagh Alavi, Mohammad Rohani, Aida Ghasemi, Ali Reza Tavasoli
The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2023)
Mahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, Ehsan Razmara, Zahra Zamani, Zahra Rezaei, Raziyeh Mashayekhi, Neda Pak, Mohammad Barzegar, Reza Azizimalamiri, Morteza Rezvani Kashani, Nahideh Khosroshahi, Maryam Rasulinezhad, Morteza Heidari, Man Amanat, Alireza Abdi, Bahram Mohammadi, Mahmoud Mohammadi, Gholam Reza Zamani, Reza Shervin Badv, Abdolmajid Omrani, Sedigheh Nikbakht, Ali Hosseini Bereshneh, Mojtaba Movahedinia, Hossein Farshad Moghaddam, Hossein Shojaaldini Ardakani, Masood Ghahvechi Akbari, Mehran Beiraghi Tousi, Mohammad Vafaee Shahi, Firouzeh Hosseini, Masoud Hassanvand Amouzadeh, Seyed Ahmad Hosseini, Ali Nikkhah, Ali Khajeh, Hooman Alizadeh, Bahram Yarali, Mohammad Rohani, Parviz Karimi, Hadi Montazer Lotf Elahi, Seyyed Mohamad Mahdi Hosseiny, Masoumeh Sadat Sadeghzadeh, Hossein Mohebbi, Maryam Hosseini Moghadam, Hajar Aryan, Hassan Vahidnezhad, Mahdieh Soveizi, Bahareh Rabbani, Ali Rabbani, Nejat Mahdieh, Masoud Garshasbi, Ali Reza Tavasoli
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry. Neurogenetics (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)
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients. Orphanet journal of rare diseases 18 (1) (2023)
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients. Orphanet journal of rare diseases 18 (1) (2023)
Franziska Paul, Calista Ng, Umar Bin Mohamad Sahari, Shahriar Nafissi, Yalda Nilipoor, Ali Reza Tavasoli, Carine Bonnard, Pui-Mun Wong, Nasrinsadat Nabavizadeh, Umut Altunoğlu, Mehrdad A Estiar, Charles B L M Majoie, Hane Lee, Stanley F Nelson, Ziv Gan Or, Guy A Rouleau, Paul P Van Veldhoven, Rami Massie, Raoul C Hennekam, Ariana Kariminejad, Bruno Reversade
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder. Human molecular genetics 31 (21) (2022)
Hajar Aryan, Shaghayegh Zokaei, Dariush Farhud, Mohammad Keykhaei, Mahmoud Reza Ashrafi, Maryam Rasulinezhad, Seyyed Mohammad Mahdi Hosseini, Ehsan Razmara, Ali Reza Tavasoli
Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly. Irish journal of medical science 191 (6) (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)
Erfan Heidari, Ehsan Razmara, Sareh Hosseinpour, Ali Reza Tavasoli, Masoud Garshasbi
Homozygous in-frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family. Annals of human genetics 84 (4) (2020)
Maryam Masoudi, Ali Hosseini Bereshneh, Maryam Rasoulinezhad, Mahmoud Reza Ashrafi, Masoud Garshasbi, Ali Reza Tavasoli
Leukoencephalopathy in Al-Raqad syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS. American journal of medical genetics. Part A 182 (10) (2020)
Afrooz Sepahvand, Ehsan Razmara, Fatemeh Bitarafan, Mohammad Galehdari, Ali Reza Tavasoli, Navid Almadani, Masoud Garshasbi
A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family. Molecular genetics & genomic medicine 8 (10) (2020)
Zahra Rezaei, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Nejat Mahdieh, Houman Alizadeh, Masoud Mohammadpour, Nahideh Khosroshahi, Man Amanat, Ali Reza Tavasoli
Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients. Neuropediatrics 50 (2) (2019)
Parastoo Rostami, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Houman Alizadeh, Masoud Garshasbi, Ali Reza Tavasoli
Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature review. Acta neurologica Belgica 120 (3) (2019)
Abdolmajid Omrani, Mohammad Rohani, Sareh Hosseinpour, Ali Reza Tavasoli
Persistent dystonia and basal ganglia involvement following metronidazole induced encephalopathy. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41 (4) (2019)
Reyhaneh Kameli, Man Amanat, Zahra Rezaei, Sareh Hosseionpour, Sedigheh Nikbakht, Houman Alizadeh, Mahmoud Reza Ashrafi, Abdolmajid Omrani, Masoud Garshasbi, Ali Reza Tavasoli
RNASET2-deficient leukoencephalopathy mimicking congenital CMV infection and Aicardi-Goutieres syndrome: a case report with a novel pathogenic variant. Orphanet journal of rare diseases 14 (1) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Ali Reza Tavasoli