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
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
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