Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Genetic Homogeneity of a Tdp1 Variant, C.1478A>G, As the Main Disease-Causing Variant of Spinocerebellar Ataxia With Axonal Neuropathy 1 (Scan1) in the Middle East: A Systematic Review
Parastoo Rostami
Parastoo Rostami

Associate Professor of Pediatric Endocrinology & Metabolism

Department Pediatrics

School of Medicine

Childrens Medical Center

Growth and Development Research Center

Tehran University of Medical Sciences

All Documents
5. Pediatric Endocrinopathies Related to Covid-19: An Update, World Journal of Pediatrics (2023)