JOURNAL OF PEDIATRIC NEUROLOGY
Official Journal of the World Pediatric Society, Turkiye
30th Annual Meeting of European Academy of Childhood Disability (EACD) will take place in Tbilisi, Georgia, May 28-31, 2018, https://www.eacd2018.net
LAST ISSUE
Reviewers' List
Contributing Reviewers in 2019
Review Article
Gadoth, Natan:
Change in Head Shape of Newborn InfanOmega-3 Supplementation for Children with Learning Difficulties and Attention Deficit Disorder: Is it Beneficial?
Goraya, Jatinder S.:
Evaluation of a Child with Spells: A “Prefixed” Approach
Original Article
Kakkar, Shruti; Sahni, Suhalika Singla; Kumar, Ruchika; Goraya, Jatinder Singh:
Vitamin D Deficiency: A Treatable but Often Forgotten Cause of Motor Delay in Infants
Mukhtiar, Khairunnisa; Ibrahim, Shahnaz; Ahmed, Mukhtiar:
Application of ICF-CY Core Sets in Children with Spastic Cerebral Palsy
Murtezani, Ardiana; Abazi, Nerimane; Sllamniku, Sabit; Rrecaj-Malaj, Shkurta; Kepuska, Arbnora B.:
Duration and Success of Nerve Rehabilitation after Elbow Injuries in Children
Case Report
Ben-Haim, Revital; Heyman, Eli; Benyamini, Lilach; Shapira, Daniel; Lev, Dorit; Tzadok, Michal; Lerman-Sagie, Tally; Saitsu, Hirotomo; Matsumoto, Naomichi; Iwama, Kazuhiro; Lazinger, Mirit; Bassan, Haim:
CHAMP1 Mutations cause Refractory Infantile Myoclonic Epilepsy
Ou, Yali; Xiang, Bingwu; Yang, Liu; Chen, Wei; Chen, Xiang; Cai, Tao:
A De novo Loss-of-Function Mutation in PAFAH1B1 Identified in a Single Case with Agyria–Pachygyria Complex
Charkhand, Behshad; Liu, Natarie; Barrett, Karlene T.; Al-Hertani, Walla; Scantlebury, Morris H.:
An Unusual Case of Infantile Spasms Due to a Pathogenic Variant in the MECP2 Gene
Dennison, John V.; Tailor, Dharmesh R.:
Cerebellar Agenesis: A Case to Remember
Mete, Mesut; Selçuki, Mehmet:
Constipation as a Rare Cause of Ventriculoperitoneal Shunt Dysfunction: A Case Report
Letter to the Editor
Joob, Beuy; Wiwanitkit, Viroj:
Diagnosis of Peroxisomal Disorders
Panigrahi, Inusha; Angurana, Suresh Kumar; Suthar, Renu:
Reply to the Letter: “Diagnosis of Peroxisomal Disorders”