DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Ausgabe 01 · Volume 19 · Februar 2021 DOI: 10.1055/s-011-50248

Reviewers' List

  • i

    Contributing Reviewers in 2020

    • Erratum

  • e1
    Açıkel, Sadettin Burak; Bilgiç, Ayhan; Derin, Hatice; Eroğlu, Arzu; Akça, Ömer Faruk; Çaksen, Hüseyin:

    Comparison of Children with Migraine and Those with Tension-Type Headache for Psychiatric Symptoms and Quality of Life

    • Review Article

  • 001
    Tornali, Cristina; Migliore, Marcello; Polizzi, Agata; Bragazzi, Nicola L.; Martini, Mariano; Ruggieri, Martino; Praticò, Andrea D.; Vecchio, Ignazio:

    Reconstructive Surgery in Children with Down Syndrome: Bioethical Implications

    • Original Article

  • 007
    Oke, Oluwasola Julius; Ajite, Adebukola; Oluwayemi, Oluwadare Isaac; Olatunya, Oladele Simeon; Ogundare, Ezra Olatunde; Abdulraheem, Fadlulai Olaoluwa:

    Malaria Infection as a Leading Cause of Febrile Seizures among Children with Seizures in Ekiti State University Teaching Hospital, Ado Ekiti, Nigeria

  • 014
    Açıkel, Burak Sadettin; Bilgiç, Ayhan; Derin, Hatice; Eroğlu, Arzu; Akça, Ömer Faruk; Çaksen, Hüseyin:

    Comparison of Children with Migraine and Those with Tension-Type Headache for Psychiatric Symptoms and Quality of Life

    • Case Report

  • 024
    Voss-Hoynes, Heather A.; Mahfooz, Naeem; Ostwani, Waseem:

    A 17-Year-Old Male with Large Retropharyngeal Neurofibroma as the Only Symptom of Neurofibromatosis Type 1 (NF1): A Case Report and Review of Literature

  • 028
    Goswami, Jyotindra Narayan; Roy, Shuvendu:

    ALG-9 Congenital Disorder of Glycosylation: A Patient with Novel Variants and No Dysmorphism

  • 031
    Carosella, Christopher M.; Smith, David F.; Sarber, Kathleen M.; Turner, Michele; Dye, Thomas J.:

    Vagus Nerve Stimulator–Associated Sleep Disordered Breathing: Identification, Treatment, and Outcomes in a Pediatric Patient

  • 036
    Fadilah, Ala; Mordekar, Santosh R.; Matthai, Sona:

    Mutation in KCNJ2 Gene in a Boy with Atypical Features of Andersen–Tawil Syndrome, ADHD, and ASD: An Expanding Phenotype

  • 040
    Maria, Arti; Bandyopadhyay, Tapas:

    Extremely Elevated Cerebrospinal Fluid Protein and Glucose Level in a Neonate with Hypernatremic Dehydration

  • 043
    Çiçek, Muharrem; Kılıç, Zeynep; Mercen, Yezdanşer; Karaoğlan, Emel; Öztarhan, Kazım:

    A Rare Cause of Facial Paralysis in Children: A Case of Ramsay Hunt Syndrome

  • 046
    Cammarata-Scalisi, Francisco; Willoughby, Colin Eric; Lacruz- Rengel, María Angelina; Bertini, Enrico Silvio; Callea, Michele:

    Pierquin Syndrome: Report of a New Case

  • 050
    Sheikh-Hosseini, Motahareh; Moarefzadeh, Mohammad; Alavi-Moghaddam, Hamideh; Morovvati, Saeid:

    A Novel Mutation in Aicardi–Goutières' Syndrome: A Case Report

  • 054
    Bouattour, Nadia; Kamoun, Fatma; Charfi, Slim; Nsir, Siham Ben; Bouchaala, Wafa; Boudawara, Tahya; Triki, Chahnez:

    Neurological Nuance: Sporadic Burkitt's Lymphoma Presenting with Guillain–Barre Syndrome

  • 059
    Bhattacharjee, Indrani; Friedman, Neil; Rodriguez, Ricardio J.:

    Utility of Rapid Exome Sequencing in the Diagnosis of a Rare Congenital Myasthenic Syndromes in a Preterm Infant

    • Rapid Communication

  • 062
    Jaseja, Harinder:

    Management of Spasticity in Cerebral Palsy: An Electroencephalogram-Oriented Novel Approach

    • Letter to the Editor

  • 065
    Prasun, Pankaj:

    Triheptanoin in Pyruvate Dehydrogenase Deficiency