Vol 12, No 1 (2018)

IJCN

Issue XML

Table of Contents

Review Article

Effect of whole exome sequencing in diagnosis of inborn errors of metabolism and neurogenetic disorders: A review articles PDF XML
Marjan Shakiba, Mohammad keramatipour 7-15

Research Article

Clinical and Imaging Findings in Childhood Posterior Reversible Encephalopathy Syndrome PDF XML
Betul Kilic 16-25
Evaluating of psychiatric behavior in obese children and adolescents PDF XML
Fatemeh Mohareri, Samaneh Noroozi Asl, Fatemeh Behdani, Nosrat Ghaemi 26-36
Haplotype analysis of DXS548 and FRAXAC1 microsatellite loci in Iranian patients with Fragile X Syndrome PDF XML
seyed ahmad Aleyasin, Fatemeh Salamat, Mojgan Mirakhori 37-46
A randomised clinical trial of efficacy of melatonin and amitriptyline in migraine prophylaxis of children PDF XML
Razieh Fallah, Fatemeh Fazeli Shoroki, Leila Sekhavat 47-54
The relationship of Parental Pain Catastrophizing with Parents Reports of Children’s Anxiety, Depression and Headache Severity PDF XML
Ghazaleh Akbarzadeh, Hojat Daniali, Mohsen Javadzadeh, Line Caes, Seyran Ranjbar, Mojtaba Habibi 55-66
Factors influencing the attendance of preterm infants to neonatal follow up and early intervention services following discharge from NICU during first year of life in Iran PDF XML
aida ravarian, roshanak vameghi, mohammad heidarzadeh, shahin nariman, setareh sagheb, fariba noori, farhoud saeed ershadi, mehdi noroozi 67-76
Bone mineral density and bone metabolism in patients with Duchenne muscular dystrophy PDF XML
Mohammad Barzegar, Elnaz NIKNAM, Parinaz HABIBI, Shadi SHIVA, Sanaz TAHMASEBI 77-83

Neurometabolic Disorder Articles

Recurrent stroke in a child with TRMA syndrome and SLC19A2 gene mutation PDF XML
Parvaneh Karimzadeh, Toktam Moosavian, Hamidreza Moosavian 84-88

Case Report

Rare Presentation of MoyaMoya Disease with Sub acute Presentation: A Case Report from Iran PDF XML
Payam Sasan nejad, Fateme Rezaei, Reza Bidaki, Ehsan Zarepur 89-93
Characterization of a de novo constitutional balanced translocation PDF XML
Javad Karim Zad Hagh, Soraya Saleh Gargari, Mir Davood Omrani 94-100
Brain Atrophy and Hypomyelination Associated with Iatrogenic Cushing’s Syndrome in an Infant PDF XML
Sumeyra Dogan, Mehmet S. Dogan, Filiz Tutunculer, Ozge Yapici Ugurlar, Hakan Genchellac 101-104
Type 0 Spinal Muscular Atrophy in rare association with congenital contracture and generalized osteopenia: A Case Report PDF XML
Aditi Singh, Poonam Dalal, Jasbir Singh, Pooja Tripathi 105-108

Letter to Editor

The Survey of Saliva Compositional Alterations is a Non- Invasive Method in Determining of Multiple Sclerosis Progression in Children PDF XML
mohamad javad saeedi borujeni, Erik Schaeffner, Shayan Golkar, Mehdi Salehi, Bahman Rashidi 109-110