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
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Review's List
Contributing Reviewers in 2020
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
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
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
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
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
Goswami, Jyotindra Narayan; Roy, Shuvendu:
ALG-9 Congenital Disorder of Glycosylation: A Patient with Novel Variants and No Dysmorphism
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
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
Maria, Arti; Bandyopadhyay, Tapas:
Extremely Elevated Cerebrospinal Fluid Protein and Glucose Level in a Neonate with Hypernatremic Dehydration
Çiçek, Muharrem; Kılıç, Zeynep; Mercen, Yezdanşer; Karaoğlan, Emel; Öztarhan, Kazım:
A Rare Cause of Facial Paralysis in Children: A Case of Ramsay Hunt Syndrome
Cammarata-Scalisi, Francisco; Willoughby, Colin Eric; Lacruz- Rengel, María Angelina; Bertini, Enrico Silvio; Callea, Michele:
Pierquin Syndrome: Report of a New Case
Sheikh-Hosseini, Motahareh; Moarefzadeh, Mohammad; Alavi-Moghaddam, Hamideh; Morovvati, Saeid:
A Novel Mutation in Aicardi–Goutières' Syndrome: A Case Report
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
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
Jaseja, Harinder:
Management of Spasticity in Cerebral Palsy: An Electroencephalogram-Oriented Novel Approach
Letter to the Editor
Prasun, Pankaj:
Triheptanoin in Pyruvate Dehydrogenase Deficiency