Alireza Tavasoli

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Pediatric Headache Fellowship

Phoenix Children's Hospital

United States

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Recent Grants

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Evaluation of natural history, clinical, demographic, genomic and radiologic characteristics of childhood heritable white matter disorders (leukodystrophies)

Open Date: 2020-08-01

Close Date: 2022-08-01

Grant: Close

Survey of Miglustat Therapeutic Effects on Neurological and Systemic Symptoms of Infantile Type of Sandhoff and Taysachs Diseases

Open Date: 2019-01-01

Close Date: 2022-03-01

Grant: Close

The first festival of outstanding researchers of Children's Medical Center

Open Date: 2017-01-01

Close Date: 2018-01-01

Grant: Close

Evaluation of natural history, clinical, demographic, genomic and radiologic characteristics of mitochondrial leukodystrophies

Open Date: 2016-05-01

Close Date: 2020-10-01

Articles (10)

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2024

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2023

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2023

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2023

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2023

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2023

Collaborators (2)

Hassan Vahidnezhad

Incoming Associate professor

Children's Hospital of Philadelphia

UNITED STATES

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Davide Tonduti

Assistant Professor

Università degli Studi di Torino

ITALY

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Alireza Tavasoli

Research Interests

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Recent Grants

Articles (10)

Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease

A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies

Effectiveness of Electronic Learning Courses on Neurologist Knowledge of Epilepsy Classification: A Study Based on the Kirkpatrick Model

Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant

Persistent basal ganglia involvement in aminoacylase-1 deficiency: expanding imaging findings and review of literature

The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families

Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage.

Evaluation of the Effectiveness of Risperidone in Treating Breath-Holding Spells in Children.

High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.

Collaborators (2)

Hassan Vahidnezhad

Davide Tonduti

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