DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 03 · Volume 19 · June 2021 DOI: 10.1055/s-011-51010

Review Article

  • 143
    Jain, Reena; Aulakh, Roosy:

    Pediatric Ocular Myasthenia Gravis: A Review

    • Original Article

  • 153
    Prasad, Asuri Narayan; Corbett, Bradley:

    Neurodevelopmental Disabilities in Canadian Children: Prevalence Data from the National Longitudinal Study of Children and Youth

  • 161
    Aprasidze, Tatia; Tatishvili, Nana; Shatirishvili, Teona; Lomidze, Giorgi:

    Predictors of Neurological Outcome of Arterial Ischemic Stroke in Children

  • 166
    Abdollahi, Morteza; Abbasi-Kangevari, Mohsen; Kolahi, Ali-Asghar; Farsar, Ahmad-Reza:

    Comparison of Health-Related-Quality-of-Life among Children with Epilepsy and a Healthy Control Group in Tehran

    • Case Report

  • 173
    Niño-Taravilla, Carmen; García-Salido, Alberto; Leoz-Gordillo, Inés; García-Campos, María Teresa; Márquez-Pérez, Trinidad Magdalena; Rozas-Gómez, Isabel; Serrano-González, Ana:

    Intracranial Injury after a Dog Attack in a Neonate

  • 177
    Elnahry, Ayman G.; Gamal Eldin, Aisha A.; Elnahry, Aya G.; Elnahry, Gehad A.:

    Concomitant Congenital Horner and Harlequin Syndromes: Case Report and Review of Literature

  • 180
    Kara, Bülent; Gül, Sedat; Güneş, Ayfer Sakarya; Mülayim, Serap; Yeşil, Gözde:

    A Novel Mutation of HINT1 Gene in an Adolescent Female with Axonal Neuropathy and Neuromyotonia

  • 183
    Nagappa, Madhu; Vandana, V.P.; Chiplunkar, Shwetha; Govindaraj, Periyasamy; Ponmalar, J.N. Jessiena; Gayathri, Narayanappa; Sinha, Sanjib; Taly, Arun B.; Sankaran, Bindu Parayil:

    Infantile Onset Encephalomyopathy, Heart Block, and Sensorineural Hearing Loss: RMND1-Associated Mitochondrial Disease

  • 189
    Stunnenberg, Bas; Ponson-Wever, Maria; Verberne, Eline; Peters, Ivo; Gerrits, Monique; Haaxma, Charlotte; van Haelst, Mieke:

    Novel SCN9A Mutations in a Compound Heterozygous Girl with Congenital Insensitivity to Pain

  • 193
    Kishnani, Sujata; Riley, Kacie; Mikati, Mohamad A.; Jiang, Yong-hui:

    Phenotypic Variability of an Inherited Pathogenic Variant in CIC Gene: A New Case Report in Two-Generation Family and Literature Review

    Supplementary Material (PDF)
  • 202
    Farrier, David; Sandweiss, Alexander J.; Bartlett, Brittnie; Abid, Farida:

    Potential Role of Growth Hormone in a Pediatric Transient Ischemic Attack

  • 204
    Koul, Roshan; Vijay, Priti; Khanna, Rajeev; Alam, Seema:

    Focal Ballismus (Right Arm) in a Boy with Wilson's Disease

    Video available
  • 207
    Soto Insuga, Victor; Cantarín-Extremera, Verónica; Solís-Muñoz, Inés; Buendía-Martínez, Silvia; Atencia-Ballesteros, María; Bernardino, Beatriz; Ruiz Falcó, María Luz:

    Pseudotumor Cerebri Caused by SARS-CoV-2 Infection in a Boy

  • 210
    Kamali Aghdam, Mojtaba; Bakhtiari, Hassan; Diaz, Diana Noemi; Eftekhari, Kambiz:

    Neurological Manifestations of Novel Coronavirus Disease in a 2-Month-Old Infant: A Case Report

  • 213
    Keçeli, Merter:

    Imaging Findings of Septooptic Dysplasia and Joubert's Syndrome in A Patient with Mixed Gonadal Dysgenesis: A New Coexistence?

    • Letter to the Editor

  • 217
    Mohandoss, Vichithra; Kumar, Vinod; Vyas, Sameer; Saini, Arushi Gahlot:

    Dengue Encephalitis: Don't Forget to List It when the Brain Is Hit