DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 34 · October 2003 DOI: 10.1055/s-002-2901

Review Article

  • 225
    Wilke, M.; Holland, S. K.; Myseros, J. S.; Schmithorst, V. J.; Ball, W. S.:

    Functional Magnetic Resonance Imaging in Pediatrics

  • Original Article

  • 234
    Nakayama, J.; Hamano, K.; Iwasaki, N.; Ohta, M.; Nakahara, S.; Matsui, A.; Arinami, T.:

    Mutation Analysis of the Leucine-Rich, Glioma Inactivated 1 Gene (LGI1) in Japanese Febrile Seizure Patients

  • 237
    Wilken, B.; Dechent, P.; Brockmann, K.; Finsterbusch, J.; Baumann, M.; Ebell, W.; Korenke, G. C.; Pouwels, P. J. W.; Hanefeld, F. A.; Frahm, J.:

    Quantitative Proton Magnetic Resonance Spectroscopy of Children with Adrenoleukodystrophy Before and After Hematopoietic Stem Cell Transplantation

  • 247
  • 253
    Kölker, S.; Hoffmann, G. F.; Schor, D. S. M.; Feyh, P.; Wagner, L.; Jeffrey, I.; Pourfarzam, M.; Okun, J. G.; Zschocke, J.; Baric, I.; Bain, M. D.; Jakobs, C.; Chalmers, R. A.:

    Glutaryl-CoA Dehydrogenase Deficiency: Region-Specific Analysis of Organic Acids and Acylcarnitines in post mortem Brain Predicts Vulnerability of the Putamen

  • Short Communication

  • 261
    Horstmann, M.; Neumaier-Probst, E.; Lukacs, Z.; Steinfeld, R.; Ullrich, K.; Kohlschütter, A.:

    Infantile Cobalamin Deficiency with Cerebral Lactate Accumulation and Sustained Choline Depletion

  • 265
    Desguerre, I.; Pinton, F.; Nabbout, R.; Moutard, M. L.; N'Guyen, S.; Marsac, C.; Ponsot, G.; Dulac, O.:

    Infantile Spasms with Basal Ganglia MRI Hypersignal May Reveal Mitochondrial Disorder Due to T8993G MT DNA Mutation

  • 270
    Horváth, J.; Ketelsen, U.-P.; Geibel-Zehender, A.; Boehm, N.; Olbrich, H.; Korinthenberg, R.; Omran, H.:

    Identification of a Novel LAMP2 Mutation Responsible for X-Chromosomal Dominant Danon Disease

  • Letter to the Editor

  • 274
  • 276
  • 278
    Auvin, S.; Cuvellier, J. C.; Vallée, L.:

    Isolated Recurrent Palatal Palsy in a Child