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