DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 01 · Volume 18 · February 2020 DOI: 10.1055/s-010-45684

Reviewers' List

  • i

    Contributing Reviewers in 2019

    • Review Article

  • 001
    Gadoth, Natan:

    Omega-3 Supplementation for Children with Learning Difficulties and Attention Deficit Disorder: Is it Beneficial?

  • 007
    Goraya, Jatinder S.:

    Evaluation of a Child with Spells: A “Prefixed” Approach

    • Original Article

  • 013
    Kakkar, Shruti; Sahni, Suhalika Singla; Kumar, Ruchika; Goraya, Jatinder Singh:

    Vitamin D Deficiency: A Treatable but Often Forgotten Cause of Motor Delay in Infants

  • 017
    Mukhtiar, Khairunnisa; Ibrahim, Shahnaz; Ahmed, Mukhtiar:

    Application of ICF-CY Core Sets in Children with Spastic Cerebral Palsy

  • 022
    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

  • 027
    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

    Supplementary Material (PDF)
  • 033
    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

  • 039
    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

  • 045
    Dennison, John V.; Tailor, Dharmesh R.:

    Cerebellar Agenesis: A Case to Remember

  • 049
    Mete, Mesut; Selçuki, Mehmet:

    Constipation as a Rare Cause of Ventriculoperitoneal Shunt Dysfunction: A Case Report

    • Letter to the Editor

  • 053
    Joob, Beuy; Wiwanitkit, Viroj:

    Diagnosis of Peroxisomal Disorders

  • 054
    Panigrahi, Inusha; Angurana, Suresh Kumar; Suthar, Renu:

    Reply to the Letter: “Diagnosis of Peroxisomal Disorders”