DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 34 · April 2003 DOI: 10.1055/s-002-2613

Original Article

  • 57
    Möller, H. E.; Koch, H. G.; Weglage, J.; Freudenberg, F.; Ullrich, K.:

    Investigation of the Cerebral Energy Status in Patients with Glutaric Aciduria Type I by 31P Magnetic Resonance Spectroscopy

  • 61
    Guzzetta, A.; Mercuri, E.; Rapisardi, G.; Ferrari, F.; Roversi, M. F.; Cowan, F.; Rutherford, M.; Paolicelli, P. B.; Einspieler, C.; Boldrini, A.; Dubowitz, L.; Prechtl, H. F. R.; Cioni, G.:

    General Movements Detect Early Signs of Hemiplegia in Term Infants with Neonatal Cerebral Infarction

  • 67
    Mäenpää, H.; Salokorpi, T.; Jaakkola, R.; Blomstedt, G.; Sainio, K.; Merikanto, J.; von Wendt, L.:

    Follow-Up of Children with Cerebral Palsy after Selective Posterior Rhizotomy with Intensive Physiotherapy or Physiotherapy Alone

  • 72
    Vermeulen, R. J.; Fetter, W. P. F.; Hendrikx, L.; Van Schie, P. E. M.; van der Knaap, M. S.; Barkhof, F.:

    Diffusion-Weighted MRI in Severe Neonatal Hypoxic Ischaemia: The White Cerebrum

  • 77
    Vles, J. S. H.; Feron, F. J. M.; Hendriksen, J. G. M.; Jolles, J.; van Kroonenburgh, M. J. P. G.; Weber, W. E. J.:

    Methylphenidate Down-Regulates the Dopamine Receptor and Transporter System in Children with Attention Deficit Hyperkinetic Disorder (ADHD)

  • 81
    Yoshinaga, H.; Ogino, T.; Endo, F.; Yasuhara, S.; Murakami, N.; Ohtsuka, Y.; Oka, E.:

    Longitudinal Study of Auditory Brainstem Response in Leigh Syndrome

  • 87
    Tulinius, M.; Moslemi, A.-R.; Darin, N.; Westerberg, B.; Wiklund, L.-M.; Holme, E.; Oldfors, A.:

    Leigh Syndrome with Cytochrome-c Oxidase Deficiency and a Single T Insertion nt 5537 in the Mitochondrial tRNATrp Gene

    • Short Communication

  • 92
    Zolkipli, Z.; Hartley, L.; Brown, S.; Rutherford, M.; Cowan, F.; Mercuri, E.; Muntoni, F.:

    Occipito-Temporal Polymicrogyria and Subclinical Muscular Dystrophy

  • 96
    Breitbach-Faller, N.; Schrader, K.; Rating, D.; Wunsch, R.:

    Ultrasound Findings in Follow-Up Investigations in a Case of Aspartoacylase Deficiency (Canavan Disease)

  • 100
    Vella, S.; Kreis, R.; Lovblad, K. O.; Steinlin, M.:

    Acute Leukoencephalopathy after Inhalation of a Single Dose of Heroin

  • 105
    Engler, F.; Maeder-Ingvar, M.; Roulet, E.; Deonna, T.:

    Treatment with Sulthiame (Ospolot®) in Benign Partial Epilepsy of Childhood and Related Syndromes: An Open Clinical and EEG Study

    • Letter to the Editor

  • 110
    Anlar, B.; Vincent, A.:

    Antibodies against Muscle-Specific Kinase in Juvenile Myasthenia Gravis