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Iranian Journal of Child Neurology|October 7, 2022
Patterns of Antiepileptic Drug Reactions in Children: A Multicenter StudyParinaz Sedighi, Neda Khalili, Nastaran Khalili, et al.Iranian Journal of Child Neurology|February 9, 2021
Effect of Zinc supplementation on child development: a systematic review and metaanalysis ProtocolSoheila Shahshahani, Firoozeh Sajedi, Shiva FatollahieradIranian Journal of Child Neurology|February 9, 2021
Comparison of Definitional skills in school-age children with cochlear implants and normal hearing peersShima Hosseinabadi, Talieh Zarifian, Robab Teymouri, et al.Iranian Journal of Child Neurology|February 9, 2021
A Novel Mutation in PEX11β GeneHamid Malekzadeh, Marjan Shakiba, Mehrdad YasaeiIranian Journal of Child Neurology|December 8, 2022
The Efficacy of the Ketogenic Diet in Improving Seizures and EEG Findings in Patients with Refractory Infantile SpasmsMelika Hanifiha, Reza Shervin Badv, Maryam Mahmoudi, et al.Iranian Journal of Child Neurology|December 8, 2022
A rare presentation of Carnitine palmitoyltransferase II (CPT-2) deficiency with normal acylcarnitine profile in a 10-year-old boy with muscle weakness and bilateral hearing loss; a case reportMohammad Vafaee Shahi, Saeide Ghasemi, Leila Tahernia, et al.Iranian Journal of Child Neurology|July 20, 2021
Association of HLA-DR2-Related Haplotype (HLA-DRB5*01-DRB1*1501-DQB1*0602) in Patients with Multiple Sclerosis in Khuzestan ProvinceNooshin Delfan, Hamid Galehdari, Farideh Ghanbari Mardasi, et al.Iranian Journal of Child Neurology|July 20, 2021
Construct Validity and Reliability of the Children Participation Assessment Scale-Child version in Children with Physical DisabilitiesOmid Rostamzadeh, Malek Amini, Afsoon Hassani MehrbanIranian Journal of Child Neurology|July 20, 2021
The Frequency of Intraventricular Hemorrhage and its Risk Factors in Premature Neonates in a Hospital's NICUBehnaz Basiri, Mohammad Kazem Sabzehei, Maryam Shokouhi Solgi, et al.Iranian Journal of Child Neurology|July 20, 2021
Analysis of glucocerebrosidase (GBA) gene mutations in Iranian patients with Gaucher diseaseHadi Mozafari, Mohammad Tghikhani, Zohreh Rahimi, et al.Pageof 71