Publications by authors named "Ali Tavasoli"

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Genotype-phenotype correlations of GFAP variants in type I Alexander disease subtypes.
Tiziana Bachetti, Ylenia Vaia, Alice Grossi, Francesca Rosamilia, Enrico Bertini, Ali Reza Tavasoli

Mol Genet Metab· November 2025

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Biallelic variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.
Francesca Magrinelli, Lucie S Taylor, Sahar Sedighzadeh, Dalila Moualek, Mariasavina Severino, Ali Reza Tavasoli

Brain Commun· October 2025

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Reassessing pediatric migraine disability: Toward an updated assessment tool in the era of novel therapeutics.
Ali Reza Tavasoli, Eric V Hastriter, Robert D Little, Kavitha T Karnik, Kara S Lewis

Headache· September 2025

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Psychometric challenges and opportunities in optimizing the Infantile Neuroaxonal Dystrophy Rating Scale.
Ali Reza Tavasoli

Dev Med Child Neurol· September 2025

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A Report of Dual Presentations of Pseudo-TORCH Syndrome 1 and MCC2 Deficiency and Review of the Literature.
Ali Talea, Shiva Bayat, Golazin Shahbodagh Khan, Neda Pak, Solmaz Aziz-Ahari, Ali Reza Tavasoli

Mol Syndromol· August 2025

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Clinical characteristics and treatment outcomes in patients with Niemann-Pick disease type C (NP-C): a cross-sectional study.
Parvaneh Karimzadeh, Farzad Ahmadabadi, Vahide Zeinali, Sharareh Kamfar, Mahmoud Reza Ashrafi, Ali Reza Tavasoli

Orphanet J Rare Dis· August 2025

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Phenotypic variability and preserved cognition in a family with KCNA2-related developmental epileptic encephalopathy.
Arastoo Kaki, Maedeh Ganji, Mohammad Farid Mohammadi, Fatemeh Bahreini, Mojtaba Movahedinia, Ali Reza Tavasoli

Neurogenetics· June 2025

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Death Causes Among Iranian Children With Leukodystrophies.
Mahsa Shiva, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli

J Child Neurol· April 2025

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Trichothiodystrophy due to ERCC2 Variants: Uncommon Contributor to Progressive Hypomyelinating Leukodystrophy.
Ali Reza Tavasoli, Arastoo Kaki, Maedeh Ganji, Seyyed Mohammad Kahani, Foozhan Radmehr

Mol Genet Genomic Med· February 2025

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Rising migraine incidence in adolescents despite stable prevalence in the US: A call for further investigation.
Ali Reza Tavasoli, Reena G Rastogi, Eric V Hastriter

Headache· January 2025

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Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant.
Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Maedeh Ganji, Pouria Mohammadi, Tayyeb Bahrami, Ali Reza Tavasoli

Acta Neurol Belg· December 2024

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The Latest Developments for the Treatment of Ataxia Telangiectasia: A Narrative Review.
Ali Mehri, Mehran Beiraghi Toosi, Ali Reza Tavasoli, Maryam Saberi-Karimian

Cerebellum· December 2024

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Exploring the Phenotypic Profile of Acute Flaccid Paralysis: Insights from a Third-Level Pediatric Emergency Room.
Sareh Hosseinpour, Roxana Pazouki, Mahmoud Reza Ashrafi, Maryam Bemanalizadeh, Masood Ghahvechi Akbari, Ali Reza Tavasoli

Iran J Child Neurol· September 2024

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Identification of a Novel Homozygous GLS Gene Variant Associated with Developmental and Epileptic Encephalopathy (DEE) Type 71.
Afsaneh Bazgir, Mehdi Agha Gholizadeh, Seyyed Mohammad Kahani, Ali Reza Tavasoli, Masoud Garshasbi

Neurogenetics· July 2024

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Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease.
Thaís Armangue, Matthew T Whitehead, Davide Tonduti, Laura Farina, Ali Reza Tavasoli

AJNR Am J Neuroradiol· June 2024

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Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance.
Behnoosh Tasharrofi, Ali Najafi, Elham Pourbakhtyaran, Susan Amirsalari, Golazin Shahbodagh Khan, Ali Reza Tavasoli

Mol Biol Rep· June 2024

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A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies.
Sareh Hosseinpour, Ehsan Razmara, Morteza Heidari, Zahra Rezaei, Mahmoud Reza Ashrafi, Ali Reza Tavasoli

Brain Dev· April 2024

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The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.
Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour

Hum Genomics· April 2024

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A comparative study on prophylactic efficacy of cinnarizine and amitriptyline in childhood migraine: a randomized double-blind clinical trial.
Mehrnaz Olfat, Sareh Hosseinpour, Safdar Masoumi, Reena Gogia Rastogi, Eric Vance Hastriter, Ali Reza Tavasoli

Cephalalgia· April 2024

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Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage.
Mehrnoosh Khodaeian, Fatemeh Bitarafan, Fatemeh Garrousi, Elham Amjadi Sardehie, Neda Pak, Ali Reza Tavasoli

J Clin Lab Anal· November 2023

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High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Mahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, Ehsan Razmara, Zahra Zamani, Ali Reza Tavasoli

Neurogenetics· October 2023

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Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Mahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, Ehsan Razmara, Zahra Zamani, Ali Reza Tavasoli

Neurogenetics· October 2023

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Description of Phenotypic Heterogeneity in a -Related Family and Literature Review.
Aida Ghasemi, Ali Reza Tavasoli, Mana Khojasteh, Mohammad Rohani, Afagh Alavi

Mol Syndromol· October 2023

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Evaluation of the Effectiveness of Risperidone in Treating Breath-Holding Spells in Children.
Gholamreza Zamani, Alireza Abdi, Morteza Heydari, Mahmoud Reza Ashrafi, Ali Reza Tavasoli

Iran J Child Neurol· October 2023

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Neurologic Manifestations of Coronavirus Disease 2019 in Children: An Iranian Hospital-Based Study.
Elmira Haji Esmaeil Memar, Morteza Heidari, Homa Ghabeli, Elham Pourbakhtyaran, Roya Haghighi, Ali Reza Tavasoli

Arch Iran Med· March 2023

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