DOI: 10.1055/s-00000041


Issue 01 · Volume 34 · February 2003 DOI: 10.1055/s-002-2487

Original Article

Miossec-Chauvet, E.; Mikaeloff, Y.; Heron, D.; Merzoug, V.; Cormier-Daire, V.; de Lonlay, P.; Matthijs, G.; Van Hulle, C.; Ponsot, G.; Seta, N.: Neurological Presentation in Pediatric Patients with Congenital Disorders of Glycosylation Type Ia
Chandler, K. E.; Moffett, M.; Clayton-Smith, J.; Baker, G. A.: Neuropsychological Assessment of a Group of UK Patients with Cohen Syndrome
van der Westhuizen, F. H.; van den Heuvel, L. P.; Smeets, R.; Veltman, J. A.; Pfundt, R.; van Kessel, A. G.; Ursing, B. M.; Smeitink, J. A. M.: Human Mitochondrial Complex I Deficiency: Investigating Transcriptional Responses by Microarray
Liasis, A.; Bamiou, D.-E.; Campbell, P.; Sirimanna, T.; Boyd, S.; Towell, A.: Auditory Event-Related Potentials in the Assessment of Auditory Processing Disorders: A Pilot Study
Capone Mori, A.; Hoeltzenbein, M.; Poetsch, M.; Schneider, J. F.; Brandner, S.; Boltshauser, E.: Lhermitte-Duclos Disease in 3 Children: A Clinical Long-Term Observation

Short Communication

Letter to the Editor

Kanbayashi, T.; Abe, M.; Fujimoto, S.; Miyachi, T.; Takahashi, T.; Yano, T.; Sawaishi, Y.; Arii, J.; Szilagyi, G.; Shimizu, T.: Hypocretin Deficiency in Niemann-Pick Type C with Cataplexy