DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 33 · October 2002 DOI: 10.1055/s-002-2375

Review Article

  • 225
  • Rapid Article

  • 232
    deGrauw, T. J.; Salomons, G. S.; Cecil, K. M.; Chuck, G.; Newmeyer, A.; Schapiro, M. B.; Jakobs, C.:

    Congenital Creatine Transporter Deficiency

  • Original Article

  • 239
  • 242
  • 249
    Barisic, N.; Schmidt, C.; Sidorova, O. P.; Herczegfalvi, A.; Gekht, B. M.; Song, I.-H.; Stucka, R.; Karcagi, V.; Abicht, A.; Lochmüller, H.:

    Congenital Myasthenic Syndrome (CMS) in Three European Kinships due to a Novel Splice Mutation (IVS7 - 2 A/G) in the Epsilon Acetylcholine Receptor (AChR) Subunit Gene

  • 255
  • Short Communication

  • 262
  • 266
    Stödberg, T.; Deniz, Y.; Esteitie, N.; Jacobsson, B.; Mousavi-Jazi, M.; Dahl, H.; Zweygberg Wirgart, B.; Grillner, L.; Linde, A.:

    A Case of Diffuse Leptomeningeal Oligodendrogliomatosis Associated with HHV-6 Variant A

  • 271
  • 274