DOI: 10.1055/s-00000041


Issue 01 · Volume 51 · February 2020 · Sample Issue DOI: 10.1055/s-010-45592

Review Article

Hareb, Farid; Bertoncelli, Carlo M.; Rosello, Olivier; Rampal, Virginie; Solla, Federico: Botulinum Toxin in Children with Cerebral Palsy: An Update
Lim, Yi Ting; Mankad, Kshitij; Kinali, Maria; Tan, Ai Peng: Neuroimaging Spectrum of Inherited Neurotransmitter Disorders

Original Article

Hornemann, Frauke; Le Duc, Diana; Roth, Christian; Pfäffle, Roland; Huhle, Dagmar; Merkenschlager, Andreas: Childhood Dystonia-Parkinsonism Following Infantile Spasms—Clinical Clue to Diagnosis in Early Beta-Propeller Protein-Associated Neurodegeneration
Gburek-Augustat, Janina; Groeschel, Samuel; Kern, Jan; Beck-Woedl, Stefanie; Just, Jennifer; Harzer, Klaus; Stampfer, Miriam; Kraegeloh-Mann, Ingeborg: Comparative Analysis of Cerebral Magnetic Resonance Imaging Changes in Nontreated Infantile, Juvenile and Adult Patients with Niemann-Pick Disease Type C

Short Communication

Kortas, Aline; Schiller, Katharina; Unterholzner, Gabriele; Rauchenzauner, Markus: Accuracy of Flash Glucose Monitoring in a Patient with Dravet Syndrome on a Ketogenic Diet
Arélin, Maria; Zierz, Stephan; Ceglarek, Uta; Heinemann, Mitja; Beblo, Skadi; Merkenschlager, Andreas: Recurrent Myalgia since Early Infancy—Misleading Clinical Course in a Child with Carnitine Palmitoyltransferase-II Deficiency
Wiemer-Kruel, Adelheid; Mayer, Hans; Ewert, Peter; Martinoff, Stefan; Eckstein, Hans-Henning; Kriebel, Thomas; Bissler, John; Franz, David; Bast, Thomas: Congenital Lymphatic Malformation and Aortic Aneurysm in a Patient with TSC2 Mutation
Hopmans, Esther M.; van der Heide, Astrid; Chung, Pui Khi; Brinkman, Daniëlle; Feltkamp, Mariet C.W.; van Dijk, J. Gert; Steggerda, Sylke J.; Niks, Erik H.: Rotavirus-Induced Neonatal Epileptic Encephalopathy—A Disease Spectrum Illustrated by Monochorionic Twins
von der Hagen, Maja; Becker, Lena-Luise; Wienker, Thomas F.; Smitka, Martin; Musante, Luciana; Ropers, Hans-Hilger; Huebner, Angela; Hu, Hao; Kaindl, Angela M.: Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family—The Role of Next Generation Sequencing in Neuromuscular Disorders
Eid, Maha; Eid, Ola; Hegazy, Ibrahim; Girgis, Marian; Mohamed, Amal; Abdel-Salam, Ghada M.H.: Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion

Images in Neuropediatrics

Book Review