DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 04 · Volume 18 · August 2020 DOI: 10.1055/s-010-48895

Review Article

175
Turgut, Yaşar B.; Tosun, Ayşe F.; Yüzbaşı, Beste K.; Tunca, Hasan: Behçet's Disease from Rheumatology and Neurology Perspectives with Special Reference to Children

Original Article

182
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
185
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

190
Cecchin, Vanessa; Pellegrin, Serena; Parmeggiani, Lucio; Pescollderungg, Lydia; Mercolini, Federico: Subacute-Onset Afferent Ataxia in Childhood: A Case Report
195
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
198
Gupta, Rekha; Barton, Chris; Puri, Vinay: Acetazolamide-Induced Aseptic Meningitis in a Female Adolescent with Idiopathic Intracranial Hypertension: A Case Report
201
Joshi, Hiten; Mordekar, Santosh R.; Connolly, Daniel J.A.; Griffiths, Paul D.: Isolated Superior Cerebellar Vermis Injury: A Consequence of Hypoxic Ischemic Injury
206
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
210
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
214
Roy, Soumya: Moyamoya Syndrome in a Child with β-Thalassemia Major