DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Ausgabe 02 · Volume 14 · Juni 2016 DOI: 10.1055/s-006-32352

Original Article

051
Omole, John O.; Kuti, Bankole P.; Adedeji, Ganiyu A.; Omole, Kehinde O.; Afolabi, Mubarak A.: Prevalence and Pattern of Birth Brachial Plexus Injuries Seen in Nigeria
057
Elsayed, Riad M.; Shatla, Rania H.; Sayyah, Hala E.; Korraa, Soheir S.; Elmogy, Atef: Effects of Antiepileptic Drugs on Oxidative Stress Enzymes in Children with Epilepsy: Correlation with Child Psychopathology

Case Report

063
Mailo, Janette Alexandra; Leonard, Norma; Landeghem, Frank van; Goez, Helly: Periventricular Cysts, Developmental Impairment in a 9q21.13q21.32 Microdeletion, and a Review of the Literature
067
Katangodage, Deepika; Kaleyias, Joseph; Carr, Lucinda; Bowman, Richard; Kumar, Ajith V.: Congenital Cataracts, Facial Dysmorphism, and Neuropathy: Two Affected Siblings in the United Kingdom
072
Corcoran, Moniek S.; Soeteman, Marijn; Wennekes, Rianne J.; Weerkamp, Nico: Nystagmus as a Rare Presenting Symptom of Neuroborreliosis in a Child
075
Greco, Filippo; Pira, Alice Le; Scalora, Luisa; Catania, Roberta; Timpanaro, Tiziana; Smilari, Pierluigi; Sorge, Giovanni: Miller Fisher Syndrome Associated with Parvovirus B19 Infection in a Child
078
Lim, Yvonne Yijuan; Tapawan, Sarah Jane Corpuz; Pang, Aileen Yu-Wen; Hyland, Keith; Tay, Stacey Kiat-Hong: Secondary Cerebral Folate Deficiency Comorbidity in Neuronal Ceroid Lipofuscinosis
082
Praticò, Andrea D.; Falsaperla, Raffaele; Ruggieri, Martino; Corsello, Giovanni; Pavone, Piero: Prognostic Challenges of SCN1A Genetic Mutations: Report on Two Children with Mild Features
089
Sayed, Rafat J.; Kulkarni, Shilpa D.; Patil, Varsha A.; Garg, Meenal: Infantile Refsum Disease: A Rare Case

Erratum

093
Das, Suman; Siddhanta, Shilpi; Mondal, Kalyanbroto; Paul, Dilip Kumar; Bhattacharya, Mala; Chatterjee, Anish: Hypokalemic Quadriparesis with Electrophysiological Changes in a Child with Distal Renal Tubular Acidosis and Nephrocalcinosis