DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 35 · July 2004 DOI: 10.1055/s-002-3706

Publisher's Note

  • 261

    eFirst - Articles Published Ahead of Print

    • Original Article

  • 262
    Messina, S.; Hartley, L.; Main, M.; Kinali, M.; Jungbluth, H.; Muntoni, F.; Mercuri, E.:

    Pilot Trial of Salbutamol in Central Core and Multi-Minicore Diseases

  • 267
    Eiffert, H.; Karsten, A.; Schlott, T.; Ohlenbusch, A.; Laskawi, R.; Hoppert, M.; Christen, H.-J.:

    Acute Peripheral Facial Palsy in Lyme Disease - A Distal Neuritis at the Infection Site

  • 274
    Ohto, T.; Iwasaki, N.; Fujiwara, J.; Ohkoshi, N.; Kimura, S.; Kawade, K.; Tanaka, R.; Matsui, A.:

    The Evaluation of Autonomic Nervous Function in a Patient with Hereditary Sensory and Autonomic Neuropathy Type IV with Novel Mutations of the TRKA Gene

  • 279
    Oguz, K. K.; Anlar, B.; Senbil, N.; Cila, A.:

    Diffusion-Weighted Imaging Findings in Juvenile Metachromatic Leukodystrophy

  • 283
    Leijser, L. M.; Klein, R. H.; Veen, S.; Liauw, L.; Van Wezel-Meijler, G.:

    Hyperechogenicity of the Thalamus and Basal Ganglia in Very Preterm Infants: Radiological Findings and Short-Term Neurological Outcome

    • Short Communication

  • 290
    van der Heyden, J. J. C.; Verrips, A.; ter Laak, H. J.; Otten, B.; Fiselier, T.:

    Hypovitaminosis D-Related Myopathy in Immigrant Teenagers

  • 293
    Kors, E. E.; Vanmolkot, K. R. J.; Haan, J.; Kheradmand Kia, S.; Stroink, H.; Laan, L. A. E. M.; Gill, D. S.; Pascual, J.; van den Maagdenberg, A. M. J. M.; Frants, R. R.; Ferrari, M. D.:

    Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine Gene ATP1A2

  • 297
    Del Bigio, M. R.; Chudley, A. E.; Booth, F. A.; Pacin, S.:

    Late Infantile Onset Krabbe Disease in Siblings with Cortical Degeneration and Absence of Cerebral Globoid Cells

  • 302
    Lamont, P. J.; Thorburn, D. R.; Fabian, V.; Vajsar, J.; Hawkins, C.; Saada (Reisch), A.; Durling, H.; Laing, N. G.; Nevo, Y.:

    Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive

  • 307
    Palmér, L.; Nordborg, C.; Steneryd, K.; Åman, P.; Kyllerman, M.:

    Large-Cell Medulloblastoma in Aicardi Syndrome. Case Report and Literature Review

  • 312
    Kurian, M. A.; Hartley, L.; Zolkipli, Z.; Little, M. A.; Costigan, D.; Naughten, E. R.; Olpin, S.; Muntoni, F.; King, M. D.:

    Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with Early Onset Severe Axonal Neuropathy