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
Review Article
Jain, Reena; Aulakh, Roosy:
Pediatric Ocular Myasthenia Gravis: A Review
Orginal Article
Prasad, Asuri Narayan; Corbett, Bradley:
Neurodevelopmental Disabilities in Canadian Children: Prevalence Data from the National Longitudinal Study of Children and Youth
Aprasidze, Tatia; Tatishvili, Nana; Shatirishvili, Teona; Lomidze, Giorgi:
Predictors of Neurological Outcome of Arterial Ischemic Stroke in Children
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
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
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
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
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
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
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
Farrier, David; Sandweiss, Alexander J.; Bartlett, Brittnie; Abid, Farida:
Potential Role of Growth Hormone in a Pediatric Transient Ischemic Attack
Koul, Roshan; Vijay, Priti; Khanna, Rajeev; Alam, Seema:
Focal Ballismus (Right Arm) in a Boy with Wilson's Disease
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
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
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
Mohandoss, Vichithra; Kumar, Vinod; Vyas, Sameer; Saini, Arushi Gahlot:
Dengue Encephalitis: Don't Forget to List It when the Brain Is Hit