DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 01 · Volume 19 · February 2021 DOI: 10.1055/s-011-50248

Reviewers' List

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Contributing Reviewers in 2020

Erratum

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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

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

Letter to the Editor

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Prasun, Pankaj: Triheptanoin in Pyruvate Dehydrogenase Deficiency