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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 KeramatipourHeliyon|April 7, 2023
A novel gene mutation for multicentric osteolysis nodulosis and arthropathy: Case report and review of literatureMarjan Shakiba, Fariba AlaeiAnnals of Human Biology|February 20, 2010
Assessment of vitamin D status in healthy children and adolescents living in Tehran and its relation to iPTH, gender, weight and heightMaryam Razzaghy-Azar, Marjan ShakibaIranian Journal of Child Neurology|July 21, 2018
The Prevalence of Psychological Disorders among Children with Diabetes Aged 5-12 Years Old Referred to the Endocrinology Clinic of Mofid Hospital, Tehran, Iran in 2014-2015Ghazal Zahed, Marjan Shakiba, Kimia SeifiIranian Journal of Child Neurology|February 9, 2021
A Novel Mutation in PEX11β GeneHamid Malekzadeh, Marjan Shakiba, Mehrdad YasaeiInternational 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|March 26, 2014
Digital and dental malformation and short stature in a patient with neurological problems: a variant of the oculodentodigital dysplasia syndrome or a new syndrome?Marjan Shakiba, Habibe Nezhad Bieglari, Mohammad Reza AlaeeIranian 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.Pageof 4