DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 38 · June 2007 DOI: 10.1055/s-002-7146

Editorial

  • 111
    Rostásy, K.:

    Promising Steps Towards a Better Understanding of OMS

  • 112
    Phillips, J. P.:

    Neuroimaging in Cerebral Palsy: A Clearer Vision of Neuroplasticity

    • Rapid Communication

  • 114
    Krasenbrink, I.; Fühlhuber, V.; Juhasz-Boess, I.; Stolz, E.; Hahn, A.; Kaps, M.; Hero, B.; Blaes, F.:

    Increased Prevalence of Autoimmune Disorders and Autoantibodies in Parents of Children with Opsoclonus-Myoclonus Syndrome (OMS)

    • Original Article

  • 117
    Verhagen, M. M. M.; Alfen, N. van; Pillen, S.; Weemaes, C. M. R.; Yntema, J. L.; Hiel, J. A. P.; Laak, H. Ter; Deuren, M. van; Broeks, A.; Willemsen, M. A. A. P.:

    Neuromuscular Abnormalities in Ataxia Telangiectasia: A Clinical, Electrophysiological and Muscle Ultrasound Study

  • 122
    Molina-Carballo, A.; Muñoz-Hoyos, A.; Sánchez-Forte, M.; Uberos-Fernández, J.; Moreno-Madrid, F.; Acuña-Castroviejo, D.:

    Melatonin Increases Following Convulsive Seizures may be Related to its Anticonvulsant Properties at Physiological Concentrations

  • 126
    Matsuo, N.; Imamura, A.; Ito, R.; Sugawara, K.; Takahashi, Y.; Kondo, N.:

    The Correlation between 1H-MR Spectroscopy and Clinical Manifestation with Tuberous Sclerosis Complex

  • 130
    Juenger, H.; Linder-Lucht, M.; Walther, M.; Berweck, S.; Mall, V.; Staudt, M.:

    Cortical Neuromodulation by Constraint-Induced Movement Therapy in Congenital Hemiparesis: An fMRI Study

  • 137
    Luciano, R.; Baranello, G.; Masini, L.; Ricci, D.; Gallini, F.; Ciotti, S.; Leone, D.; Serrao, F.; Santis, M. De; Zecca, E.; Zuppa, A.; Romagnoli, C.; Rocco, C. Di; Guzzetta, F.; Mercuri, E.:

    Antenatal Post-hemorrhagic Ventriculomegaly: A Prospective Follow-up Study

    • Short Communication

  • 143
    Hartmann, H.; Herchenbach, J.; Stephani, U.; Ledaal, P.; Donnerstag, F.; Lücke, T.; Das, A. M.; Christen, H. J.; Hagedorn, M.; Meins, M.:

    Novel Mutations in Exon 6 of the GFAP Gene Affect a Highly Conserved IF Motif in the Rod Domain 2B and are Associated with Early Onset Infantile Alexander Disease

  • 148
    Lohmeier, K.; Distelmaier, F.; van den Heuvel, L. P.; Rodenburg, R. J. T.; Smeitink, J.; Mayatepek, E.; Hoehn, T.:

    Fatal Hypertensive Crisis as Presentation of Mitochondrial Complex I Deficiency

  • 151
    Anlar, B.; Oktem, F.; Bakkaloglu, B.; Haliloglu, M.; Oguz, H.; Unal, F.; Pehlivanturk, B.; Gokler, B.; Ozbesler, C.; Yordam, N.:

    Urinary Epidermal and Insulin-Like Growth Factor Excretion in Autistic Children

  • 154
    Chiodo, D. Castellano; DiRocco, M.; Gandolfo, C.; Morana, G.; Buzzi, D.; Rossi, A.:

    Neuroimaging Findings in Malignant Infantile Osteopetrosis due to OSTM1 Mutations

  • 157
    Takahashi, K.; Saitoh, M.; Hoshino, H.; Mimaki, M.; Yokoyama, Y.; Takamizawa, M.; Mizuguchi, M.; Lin, Z.-M.; Yang, Y.; Igarashi, T.:

    A Case of Primary Erythermalgia, Wintry Hypothermia and Encephalopathy

  • 160
    Huisman, T. A. G. M.; Kubat, S. H.; Eckhardt, B. P.:

    The “Dark Cerebellar Sign”