DOI : 10.1055/s-00000041


Issue 01 · Volume 35 · February 2004 DOI: 10.1055/s-002-3101

Abstracts for the 30th Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)
Bern, Switzerland, March 25–28, 2004

M. Steinlin

Vlaho, S.; Gebhardt, B.; Dittrich, S.; Raikhman, P.; Boda, V.; Kieslich, M.: Imbalance of biogenic amines in patients with compulsive disorders and tics
Baumeister, F. A. M.; Liebhaber, G.; Riemann, E.; Gempel, K.; Freisinger, P.: Efficacy of the ketogenic diet in neurometabolic disorders
Gebhardt, B.; Parbel, S.; Dittrich, S.; Vlaho, S.; Böhles, H.; Kieslich, M.: Pyruvat carboxylase deficiency – therapeutic concept of a basic defect of neurotransmission
Lücke, T.; Tzikas, D.; Kanzelmeyer, N.; Frölich, J.; Das, A. M.: Elevated concentrations of endogenous NO-synthase-antagonist ADMA in patients with citrullinemia
Haberlandt, E.; Trinka, E.; Zimmerhackl, L. B.; Baumgartner, S.; Konstantopoulou, V.; Scholl-Bürgi, S.; Felber, S.; Skladal, D.: EEG-alterations in patients with propionic acidemia
Mercimek-Mahmutoglu, S.; Ipsiroglu, O. S.; Prayer, D.; van der Knaap, M.; Stöckler-Ipsiroglu, S.: Vanishing white matter disease, a new leukoencephalopathy. Case report of 3 patients
Kieslich, M.; Gebhardt, B.; Vlaho, S.; Boda, V.; Dittrich, S.; Raikhman, P.; Bollinger, M.; Will, Heike; Schneider, W.; Fischer, Doris; Janssen, A.; Smeitink, J.; Trijbels, F.; Veldman, A.: Non lactate acidotic encephalomyopathy with ptosis, severe central apnea, isolated complex III deficiency and 15257 mutation in the cytochrome b gene – a previously undescribed mitochondrial disorder constellation
Mercimek-Mahmutoglu, S.; Edlinger-Horvat, C.; Item, C.; Stromberger, C.; Adami, A.; Appleton, R. E.; Ensenauer, R.; Fernandez, E.; Grolik, A.; Hanefeld, F.; Korall, H.; Polster, T.; Sälke-Kellermann, R.; van der Knaap, M.; Stöckler-Ipsiroglu, S.: Clinical, biochemical and molecular findings in 16 patients with GAMT deficiency
Nagel, S.; Hagel, C.; Schäfer, H.; Neumaier Probst, E.; Das, A.; Ullrich, K.; Kohlschütter, A.: Alpers-Huttenlocher syndrome: mitochondrial diseases of brain and liver
Grünewald, S.; Champion, M. P.; Leonard, J. V.; Schaper, J.; Morris, A. A. M.: Biotinidase deficiency: a treatable leukoencephalopathy
Plecko, B.; Kaltenbrunner, K.; Erwa, W.; Simbrunner, J.; Koch, H. G.; Fowler, B.: Hyperhomocysteinemia as a marker of methylentetrahydrofolate reductase deficiency in two siblings with early neurodegeneration