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ISA Transactions|September 19, 2019
Adaptive synchronization of chaotic systems with hysteresis quantizer inputMostafa Asadollahi, Amir Rikhtehgar Ghiasi, Mohammad Ali Badamchizadeh
Iranian Journal of Child Neurology|July 11, 2024
Aicardi-Goutières Syndrome Type 1: A Novel Missense Variant and Review of the Mutational SpectrumBehnoosh Tasharrofi, Parvaneh Karimzadeh, Mostafa Asadollahi, et al.
Iranian Journal of Child Neurology|September 25, 2015
Measuring Serum Level of Ionized Magnesium in Patients with MigraineFarhad Assarzadegan, Mostafa Asadollahi, Hojjat Derakhshanfar, et al.
Iranian Journal of Child Neurology|April 24, 2023
A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic ManifestationsDavoud Amirkashani, Mostafa Asadollahi, Rozita Hosseini, et al.
Iranian Journal of Neurology|November 20, 2013
Secondary headaches attributed to arterial hypertensionFarhad Assarzadegan, Mostafa Asadollahi, Omid Hesami, et al.
Nutritional Neuroscience|November 5, 2020
Evaluation of modulatory effects of saffron (Crocus sativus L.) aqueous extract on oxidative stress in ischemic stroke patients: a randomized clinical trialSaeed Gudarzi, Mahvash Jafari, Gila Pirzad Jahromi, et al.
Journal of Ethnopharmacology|March 28, 2019
Protective properties of the aqueous extract of saffron (Crocus sativus L.) in ischemic stroke, randomized clinical trialMostafa Asadollahi, Parisa Nikdokht, Boshra Hatef, et al.
Iranian Journal of Child Neurology|February 16, 2026
Decoding the Genetic Enigma: A Case Study on Congenital Anomalies with Developmental Delay and 9q Duplication Unveiled Via Comprehensive Whole Exome Sequencing and Cytogenetic AnalysisReyhaneh Dehghanzad, Mohsen Aghajanpour Mir, Zahra Golchehre, et al.
Reports of Biochemistry & Molecular Biology|October 4, 2021
Whole-Exome Sequencing Identified a Novel Variant (C.405_422+39del) in DSP Gene in an Iranian Pedigree with Familial Dilated CardiomyopathyYeganeh Eshaghkhani, Arezoo Mohamadifar, Mostafa Asadollahi, et al.
Iranian Journal of Child Neurology|February 28, 2022
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous familiesSusan Akbaroghli, Daniz Kooshavar, Zahra Golchehre, et al.
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