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Iranian Journal of Child Neurology|January 31, 2018
Effect of Whole Exome Sequencing in Diagnosis of Inborn Errors of Metabolism and Neurogenetic DisordersMarjan Shakiba, Mohammad Keramatipour
Iranian Journal of Child Neurology|February 9, 2021
A Novel Mutation in PEX11β GeneHamid Malekzadeh, Marjan Shakiba, Mehrdad Yasaei
International Journal of Hematology-Oncology and Stem Cell Research|May 29, 2020
Ghosal Hematodiaphyseal Dysplasia: A Case ReportMarjan Shakiba, Shahin Shamsian, Hamid Malekzadeh, et al.
Iranian Journal of Child Neurology|April 8, 2020
Assessment of Anthropometric Indices in Patients with PhenylketonuriaMarjan Shakiba, Mohammadreza Alaei, Hedyeh Saneifard, et al.
Iranian Journal of Child Neurology|February 3, 2025
From Diabetes to Neuropathy: A Diagnostic Journey to Leigh SyndromeArya Behzadi, Pooya Poormehr, Hedyeh Saneifard, et al.
Hepatitis Monthly|September 14, 2013
Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison SyndromeBabak Behnam, Marjan Shakiba, Ali Ahani, et al.
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