DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 01 · Volume 43 · Februar 2012 DOI: 10.1055/s-002-23003

Review Article

Original Article

010
Hirschfeld, Gerrit; Zernikow, Boris; Kraemer, Nicole; Hechler, Tanja; Aksu, Fuat; Krumova, Elena; Maier, Christoph; Magerl, Walter; Blankenburg, Markus: Development of Somatosensory Perception in Children: A Longitudinal QST-Study
017
Lotte, Jan; Haberlandt, Edda; Neubauer, Bernd; Staudt, Martin; Kluger, Gerhard Josef: Bromide in Patients with SCN1A-Mutations Manifesting as Dravet Syndrome
022
van der Lei, Hannemieke D.; Steenweg, Marjan E.; Barkhof, Frederik; de Grauw, Ton; d'Hooghe, Marc; Morton, Richard; Shah, Siddharth; Wolf, Nicole; van der Knaap, Marjo S.: Characteristics of Early MRI in Children and Adolescents with Vanishing White Matter
027
Schroeder, A. Sebastian; Kling, Theresia; Huß, Kristina; Borggraefe, Ingo; Koerte, Inga K.; Blaschek, Astrid; Jahn, Klaus; Heinen, Florian; Berweck, Steffen: Botulinum Toxin Type A and B for the Reduction of Hypersalivation in Children with Neurological Disorders: A Focus on Effectiveness and Therapy Adherence
037
Pini, Giorgio; Bigoni, Stefania; Engerström, Ingegerd Witt; Calabrese, Olga; Felloni, Beatrice; Scusa, Maria Flora; Di Marco, Pietro; Borelli, Paolo; Bonuccelli, Ubaldo; Julu, Peter O. O.; Nielsen, Jytte Bieber; Morin, Bodil; Hansen, Stig; Gobbi, Giuseppe; Visconti, Paola; Pintaudi, Maria; Edvige, Veneselli; Romanelli, Anna; Bianchi, Fabrizio; Casarano, Manuela; Battini, Roberta; Cioni, Giovanni; Ariani, Francesca; Renieri, Alessandra; Benincasa, Alberto; Delamont, Robert S.; Zappella, Michele; ESRRA group: Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases

Short Communication

044
Kau, Thomas; Veraguth, Dorothe; Schiegl, Heinrich; Scheer, Ianina; Boltshauser, Eugen: Chudley-McCullough Syndrome: Case Report and Review of the Neuroimaging Spectrum
048
Horvath, Gabriella Ana; Eichler, Florian; Poskitt, Ken; Stockler-Ipsiroglu, Sylvia: Failure of Repeated Cyclophosphamide Pulse Therapy in Childhood Cerebral X-Linked Adrenoleukodystrophy