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Fatemeh Sadat Rashidi

2PUBLICATIONS

10CO-AUTHORS

Optical technologyNeurology and neuromuscular diseases

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Publications (2)

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|Jun 01, 2026

An Autosomal Dominant <i>TUBB3</i> Mutation Associated With Congenital Fibrosis of the Extraocular Muscles Type 3 in an Iranian Family.

|Feb 24, 2023

Potential role of FKBP5 single-nucleotide polymorphisms in functional seizures.

Ali A Asadi-Pooya, Leila Simani, Marjan Asadollahi

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Frequent Collaborators

2 joint publications

Ehsan Ahmadipour

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