DOI: 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 33 · February 2002 DOI: 10.1055/s-002-1635

Abstracts

A1
Abstracts of the 28th Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie) April 4 - 7, 2002, Freiburg/Breisgau, Germany

Review Article

1
Bandmann, O.; Wood, N. W.: Dopa-Responsive Dystonia - The Story so Far

Original Article

6
Kramm, C. M.; Korholz, D.; Rainov, N. G.; Niehues, T.; Fischer, U.; Steffens, S.; Frank, S.; Banning, U.; Horneff, G.; Schroten, H.; Burdach, S.: Systemic Activation of the Immune System during Ganciclovir Treatment Following Intratumoral Herpes Simplex Virus Type 1 Thymidine Kinase Gene Transfer in an Adolescent Ependymoma Patient
10
Mercuri, E.; Counsell, S.; Allsop, J.; Jungbluth, H.; Kinali, M.; Bonne, G.; Schwartz, K.; Bydder, G.; Dubowitz, V.; Muntoni, F.: Selective Muscle Involvement on Magnetic Resonance Imaging in Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
15
Ohmori, I.; Ohtsuka, Y.; Ogino, T.; Yoshinaga, H.; Kobayashi, K.; Oka, E.: The Relationship between Paroxysmal Kinesigenic Choreoathetosis and Epilepsy
21
Kloss, S.; Pieper, T.; Pannek, H.; Holthausen, H.; Tuxhorn, I.: Epilepsy Surgery in Children with Focal Cortical Dysplasia (FCD): Results of Long-Term Seizure Outcome
27
Peters, V.; Penzien, J. M.; Reiter, G.; Körner, C.; Hackler, R.; Assmann, B.; Fang, J.; Schaefer, J. R.; Hoffmann, G. F.; Heidemann, P. H.: Congenital Disorder of Glycosylation IId (CDG-IId) - A New Entity: Clinical Presentation with Dandy-Walker Malformation and Myopathy
33
Geerdink, N.; Rotteveel, J. J.; Lammens, M.; Sistermans, E. A.; Heikens, G. T.; Gabreëls, F. J. M.; Mullaart, R. A.; Hamel, B. C. J.: MECP2 Mutation in a Boy with Severe Neonatal Encephalopathy: Clinical, Neuropathological and Molecular Findings

Short Communication

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Klingebiel, R.; Benndorf, G.; Schmitt, M.; von Moers, A.; Lehmann, R.: Large Cerebral Vessel Occlusive Disease in Lyme Neuroborreliosis
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Breukels, M. A.; Plötz, F. B.; van Nieuwenhuizen, O.; van Diemen-Steenvoorde, J. A. A. M.: Breath Holding Spells in a 3-Day-Old Neonate: An Unusual Early Presentation in a Family with a History of Breath Holding Spells
43
Eikermann, M.; Bredendiek, M.; Schaper, J.; Hövel, M.; Peters, J.: Resistance to Rocuronium in a Child with Schwartz-Jampel Syndrome Type 1 B
47
Topcu, M.; Saatci, I.; Haliloglu, G.; Kesimer, M.; Coskun, T.: D-Glyceric Aciduria in a Six-Month-Old Boy Presenting with West Syndrome and Autistic Behaviour
51
Tsukamoto, H.; Ishikawa, T.; Fujii, Y.; Fukumizu, M.; Sugai, K.; Kanbayashi, T.: Undetectable Levels of CSF Hypocretin-1 (Orexin-A) in Two Prepubertal Boys with Narcolepsy

Letter to the Editor

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Zwijnenburg, P. J. G.; Wennink, J. M. B.; Laman, D. M.; Linssen, W. H. J. P.: Alice in Wonderland Syndrome: A Clinical Presentation of Frontal Lobe Epilepsy