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Iranian Journal of Child Neurology|December 11, 2023
Evaluation of the Effectiveness of Risperidone in Treating Breath-Holding Spells in ChildrenGholamreza Zamani, Alireza Abdi, Morteza Heydari, et al.BMC Medical Genomics|September 26, 2023
Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case reportElham Salehi Siavashani, Mahmoud Reza Ashrafi, Homa Ghabeli, et al.Clinical Neurology and Neurosurgery|February 26, 2022
Methenyltetrahydrofolate synthease deficiency (MTHFS deficiency): Novel mutation and brain MRI findings: A case report and glance to other casesMohammad Vafaee-Shahi, Davoud Amirkashani, Mahmoud Reza Ashrafi, et al.Iranian Journal of Child Neurology|February 28, 2022
Hereditary Autonomic Neuropathy of the Oral Cavity and its ManagementNiloofar Esmaeilzadeh, Mahmoud Reza Ashrafi, Hossein Shojaaldini Ardakani, et al.Iranian Journal of Child Neurology|August 22, 2014
Comparison of Serum Zinc and Copper levels in Children and adolescents with Intractable and Controlled EpilepsyZeynab Kheradmand, Bahram Yarali, Ahad Zare, et al.Iranian Journal of Child Neurology|March 26, 2014
Sleep Inducing for EEG Recording in Children: A Comparison between Oral Midazolam and Chloral HydrateMahmoud Reza Ashrafi, Reza Azizi Malamiri, Gholam Reza Zamani, et al.European Child & Adolescent Psychiatry|February 18, 2009
Executive dysfunction in treated phenylketonuric patientsBahare Azadi, Arshia Seddigh, Mehdi Tehrani-Doost, et al.Iranian Journal of Child Neurology|July 13, 2017
Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo DiseasesMahmoud Reza Ashrafi, Ali Reza Tavasoli, Houman Alizadeh, et al.Brain & Development|September 5, 2006
Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiencyNima Parvaneh, Mahmoud-Reza Ashrafi, Mehdi Yeganeh, et al.Journal of Molecular Neuroscience : MN|May 29, 2026
MECP2 Variant Spectrum and Genotype-Phenotype Correlations in Iranian Rett Syndrome Patients: Identification of a Novel Frameshift MutationParnoush Booalizadeh, Iman Salahshourifar, Bahareh Rabbani, et al.Pageof 13