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Scientific Reports|April 2, 2024
Investigation of class-F power amplifier in the presence of the second and fourth harmonics of input voltageParastoo Rostami, Akram Sheikhi
Iranian Journal of Child Neurology|July 13, 2017
Neurological and Vascular Manifestations of Ethylmalonic EncephalopathyAli Reza Tavasoli, Parastoo Rostami, Mahmoud Reza Ashrafi, et al.
Acta Medica Iranica|December 13, 2017
Pericentric Inversion of Chromosome 9 in an Infant With Ambiguous GenitaliaArya Sotoudeh, Parastoo Rostami, Maryam Nakhaeimoghadam, et al.
Revista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo|May 11, 2022
A suggested screening method for hypothyroidism in very preterm and/or very low birth weight neonatesKayvan Mirnia, Sina Dindarian, Sedra Mohammadi, et al.
The Turkish Journal of Pediatrics|October 26, 2012
Insulin edema in a child with diabetes mellitus type 1Parastoo Rostami, Arya Sotoudeh, Maryam Nakhaeimoghadam, et al.
World Journal of Pediatrics : WJP|December 8, 2022
Pediatric endocrinopathies related to COVID-19: an updateElmira Haji Esmaeli Memar, Reihaneh Mohsenipour, Seyedeh Taravat Sadrosadat, et al.
Journal of Clinical Immunology|August 2, 2014
Inborn errors of metabolism underlying primary immunodeficienciesNima Parvaneh, Pierre Quartier, Parastoo Rostami, et al.
Acta Medica Iranica|January 7, 2014
Hypothalamic hamartoma in an unusual case with delayed pubertyMaryam Nakhaeimoghadam, Parastoo Rostami, Ameneh Zare-Shahabadi, et al.
Brain & Development|April 26, 2017
Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature reviewAli Reza Tavasoli, Reza Shervin Badv, Johannes Zschocke, et al.
Acta Neurologica Belgica|June 22, 2019
Primary creatine deficiency syndrome as a potential missed diagnosis in children with psychomotor delay and seizure: case presentation with two novel variants and literature reviewParastoo Rostami, Sareh Hosseinpour, Mahmoud Reza Ashrafi, et al.
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