DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 01 · Volume 51 · Februar 2020 DOI: 10.1055/s-010-45592

Review Article

  • 001
    Hareb, Farid; Bertoncelli, Carlo M.; Rosello, Olivier; Rampal, Virginie; Solla, Federico:

    Botulinum Toxin in Children with Cerebral Palsy: An Update

  • 006
    Lim, Yi Ting; Mankad, Kshitij; Kinali, Maria; Tan, Ai Peng:

    Neuroimaging Spectrum of Inherited Neurotransmitter Disorders

    • Original Article

  • 022
    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

  • 030
    Nagy, Eszter; Farkas, Nelli; Hollódy, Katalin:

    Does Co-occurred Cerebral Palsy Change the Prognosis of West Syndrome?

  • 037
    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

    Supplementary Material (PDF)

    • Short Communication

  • 045
    Kortas, Aline; Schiller, Katharina; Unterholzner, Gabriele; Rauchenzauner, Markus:

    Accuracy of Flash Glucose Monitoring in a Patient with Dravet Syndrome on a Ketogenic Diet

  • 049
    Hofmeister, Benedikt; von Stülpnagel, Celina; Berweck, Steffen; Abicht, Angela; Kluger, Gerhard; Weber, Peter:

    Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides–Baraitser Syndrome (SMARCA2 Mutation)—Due to a POLG1-Related Effect?

    Supplementary Material (PDF)
  • 053
    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

  • 057
    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

  • 062
    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

  • 068
    Zhang, Yunjian; Zhang, Linmei; Zhou, Shuizhen:

    Developmental Regression and Epilepsy of Infancy with Migrating Focal Seizures Caused by TBCD Mutation: A Case Report and Review of the Literature

    Supplementary Material (PDF)
  • 072
    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

    Supplementary Material (PDF)
  • 076
    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

  • 083
    Cramer, Natan; Manole, Mioara:

    Unresponsive 4-Year-Old Boy Found to Have X-Linked Adrenoleukodystrophy

    • Book Review

  • 085
    Boltshauser, Eugen:

    Topical Diagnosis in Neurology: Anatomy, Physiology, Signs, Symptoms