Effect of Whole Exome Sequencing in Diagnosis of Inborn Errors of Metabolism and Neurogenetic Disorders

por SHAKIBA, Marjan, KERAMATIPOUR, Mohammad
Publicado 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 2014-2015

por ZAHED, Ghazal, SHAKIBA, Marjan, SEIFI, Kimia
Publicado 2018

A Novel Mutation in PEX11β Gene

por MALEKZADEH, Hamid, SHAKIBA, Marjan, YASAEI, Mehrdad
Publicado 2021

Digital and Dental Malformation and Short Stature in a Patient with Neurological Problems: A Variant of the Oculodentodigital Dysplasia Syndrome or a New Syndrome?

por SHAKIBA, Marjan, NEZHAD BIEGLARI, Habibe, ALAEE, Mohammad Reza
Publicado 2012

Assessment of Anthropometric Indices in Patients with Phenylketonuria

por SHAKIBA, Marjan, Alaei, Mohammadreza, SANEIFARD, Hedyeh, MOSALLANEJAD, Asieh
Publicado 2020

Ghosal Hematodiaphyseal Dysplasia: A Case Report

por Shakiba, Marjan, Shamsian, Shahin, Malekzadeh, Hamid, Yasaei, Mehrdad
Publicado 2020

Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome

por Behnam, Babak, Shakiba, Marjan, Ahani, Ali, Razzaghy Azar, Maryam
Publicado 2013

Defects in Very Long-Chain Fatty Acid Oxidation Presenting as Different Types of Cardiomyopathy

por Alaei, Fariba, Shakiba, Marjan, Saneifard, Hedyeh, Vahidshahi, Kourosh, Alaei, Mastaneh
Publicado 2022

A Rare Case of Glycogen Storage Disease Type 1a Presenting with Hemophagocytic Lymphohistiocytosis (HLH)

por Saneifard, Hedyeh, Shamsian, Bibishahin, Shakiba, Marjan, Karizi Zarea, Simin, Sheikhy, Ali
Publicado 2020

Non-celiac gluten sensitivity as a rare cause of growth retardation in children: a case series study

por Saneifard, Hedyeh, Sheikhy, Ali, Karbasian, Fereshteh, Eslamian, Golnaz, Shakiba, Marjan, Babaie, Delara
Publicado 2021

Vitamin D Deficiency in Children and Adolescents: Role of Puberty and Obesity on Vitamin D Status

por Saneifard, Hedyeh, Shakiba, Marjan, Sheikhy, Ali, Baniadam, Leila, Abdollah Gorji, Fatemeh, Fallahzadeh, Aida
Publicado 2021

Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria

por SHAKIBA, Marjan, SANEIFARD, Hedyeh, ALAEI, Mohammad Reza, MOSALLANEJAD, Asieh, LOTFI, Mojtaba, YASAEI, Mehrdad, ALIZADE NADERI, Elahe
Publicado 2021

Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case report

por Shakiba, Marjan, Mahjoub, Fatemeh, Fazilaty, Hassan, Rezagholizadeh, Fereshteh, Shakiba, Arghavan, Ziadlou, Maryam, Gahl, William A., Behnam, Babak
Publicado 2016

Utility of Seizure Pattern and Related Clinical Features in the Diagnosis of Neurometabolic Disorders

por JAFARI, Narjes, MOSALLANEJAD, Asieh, GHOBADIFAR, Asieh, KARIMZADEH, Parvaneh, GHASSEMABADI, Robabeh Ghodssi, NASEHI, Mohammadmehdi, SHAKIBA, Marjan, TABATABAEE, Shahrzad
Publicado 2020

Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)

por Eghbali, Maryam, Abiri, Maryam, Talebi, Saeed, Noroozi, Zahra, Shakiba, Marjan, Rostami, Parastoo, Alimadadi, Hosein, Najafi, Mehri, Yazarlou, Fatemeh, Rabbani, Ali, Modarressi, Mohammad Hossein
Publicado 2020