DOI: 10.1055/s-00000041

Neuropediatrics

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

Abstracts

  • A1
  • Review Article

  • 1
  • 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
  • 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

  • 37
    Klingebiel, R.; Benndorf, G.; Schmitt, M.; von Moers, A.; Lehmann, R.:

    Large Cerebral Vessel Occlusive Disease in Lyme Neuroborreliosis

  • 41
    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
  • 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

  • 53
    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