DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 49 · April 2018 DOI: 10.1055/s-008-39401

Review Article

104
Juliá-Palacios, N.; Boronat, S.; Delgado, I.; Felipe, A.; Macaya, A.: Pediatric Klüver–Bucy Syndrome: Report of Two Cases and Review of the Literature

Original Article

112
Cayami, Ferdy K.; Bugiani, Marianna; Pouwels, Petra J.W.; Bernard, Geneviève; van der Knaap, Marjo S.; Wolf, Nicole I.: 4H Leukodystrophy: Lessons from 3T Imaging
118
Green, Lydia; Berry, Ian R.; Childs, Anne-Marie; McCullagh, Helen; Jose, Sandhya; Warren, Dan; Craven, Ian; Camm, Nick; Prescott, Katrina; van der Knaap, Marjo S.; Sheridan, Eamonn; Livingston, John H.: Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander Disease
123
135
Kanemura, Hideaki; Sano, Fumikazu; Ohyama, Tetsuo; Sugita, Kanji; Aihara, Masao: Effect of Levetiracetam Monotherapy in Nonlesional Focal Childhood Epilepsy
142
Haaga, Manja; Trauzettel-Klosinski, Susanne; Krumm, Anna; Küster, Stephan; Ivanov, Iliya; Cordey, Angelika; Gehrlich, Claudia; Staudt, Martin: Homonymous Hemianopia in Children and Adolescents: An MRI Study

Short Communication

150
Varvagiannis, K.; Hanquinet, S.; Billieux, M. H.; De Luca, R.; Rimensberger, P.; Lidgren, M.; Guipponi, M.; Makrythanasis, P.; Blouin, J. L.; Antonarakis, S. E.; Steinfeld, R.; Kern, I.; Poretti, A.; Fluss, J.; Fokstuen, S.: Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder
154
Srinivasaraghavan, Rangan; Parameswaran, Narayanan; Mathis, Deborah; Bürer, Celine; Plecko, Barbara: Antiquitin Deficiency with Adolescent Onset Epilepsy: Molecular Diagnosis in a Mother of Affected Offsprings

Images in Neuropediatrics

158
De Pieri, Carlo; Bravar, Giulia; Dolcemascolo, Valentina; Dallorto, Anna; De Colle, Maria Cristina; Cogo, Paola Elisa: Hoofbeats, Zebras, and a Child with Vomiting

Book Review

161
Neubauer, Bernd A.: Rett Syndrome