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

Volume 18, Number 4, Year 2020


Review Article
Turgut, Yaşar B.; Tosun, Ayşe F.; Yüzbaşı, Beste K.; Tunca, Hasan:


Original Article
Koul, Roshan; Naiha Al Harousi, Saleem Saleh; AlNabhani, Sousan; AlFutaisi, Amna:
Vincristine Neuropathy in Children: Squatting (Sitting Cross Legged) Predisposes Common Peroneal Nerves to Be More Severely Affected than Tibial Nerves


Sertpoyraz, Filiz Meryem; Tiftikcioglu, Bedile Irem; Baydan, Figen; Tuncay, Bakiye; Gunduz, Nihan Erdinc; Dikici, Aylin; Zorlu, Yasar:
Relationship of Scoliosis with Pain and Respiratory Dysfunction in Patients with Duchenne Muscular Dystrophy


Case Report
Cecchin, Vanessa; Pellegrin, Serena; Parmeggiani, Lucio; Pescollderungg, Lydia; Mercolini, Federico:
Subacute-Onset Afferent Ataxia in Childhood: A Case Report


Barbut, Gal; Brosgol, Yuri; Celiker, Mahmut; Stein, Evan G.; McAbee, Gary N.:
Thoracic Endodermal Sinus Tumor with Root Compression Mimicking Guillain–Barre Syndrome in Clinical Presentation, CSF Studies, and EMG/NCV Findings


Gupta, Rekha; Barton, Chris; Puri, Vinay:
Acetazolamide-Induced Aseptic Meningitis in a Female Adolescent with Idiopathic Intracranial Hypertension: A Case Report


Joshi, Hiten; Mordekar, Santosh R.; Connolly, Daniel J.A.; Griffiths, Paul D.:
Isolated Superior Cerebellar Vermis Injury: A Consequence of Hypoxic Ischemic Injury


Portale, Anna; Mazzurco, Marina; Portale, Laura; Pavone, Piero; Bertini, Enrico; Polizzi, Agata; Praticò, Andrea D.; Ruggieri, Martino:
Aicardi–Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations


Harada, Yohei; Sorensen, Seth T.; Aravindhan, Akilandeswari; Stefans, Vikki; Veerapandiyan, Aravindhan:
Dystrophinopathy in a Family Due to a Rare Nonsense Mutation Causing Predominant Behavioral Phenotype


Roy, Soumya:
Moyamoya Syndrome in a Child with β-Thalassemia Major