DOI : 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 37 · June 2006 DOI: 10.1055/s-002-5127


Abstracts of the 32nd Annual Meeting – of the Society for Neuropediatrics – (Gesellschaft für Neuropädiatrie)
Mannheim, Germany, 20–24, September 2006

D. Karch – J. Pietz
Abstracts (HTML) List of Authors
P1165
Kröll, J.; Sälke-Kellermann, R. A.; Martin, E.; Huismann, T.; Boltshauser, E.: PEHO syndrome: well described but easily missed
P1166
Brocke, K. S.; Hahn, G.; Heubner, G.; Kohlschütter, A.; van der Knaap, M. S.; von der Hagen, M.: Progressive ataxia and symptomatic epilepsy in a case of leukoencephalopathy with brainstem and spinal cord involvement
P1167
Wilmsmeyer, M.; Königs, I.; Bendl, C.; König, S.: Smith-Lemli-Opitz syndrome: case report on two patients with different clinical presentation
P1168
Pohl, D.; Brockmann, K.; Rustenbeck, H. H.; Hanefeld, F.: Leigh syndrome: an uncommon manifestation caused by biotinidase-deficiency
P1169
Gebhardt, B.; Parbel, S.; Dittrich, S.; Vlaho, S.; Kieslich, M.: Successful anticonvulsive therapy with D/L 3-hydroxybutyrate and ketogenic diet in a boy with agininosccinate lyase deficiency and status epileptics minor
P1170
Brunner-Krainz, M.; Eber, E.; Percy, M. J.; Gruber-Sedlmayr, U.; Plecko, B.: Congenital methemoglobinemia type II (RCM II): an inherited neurodegenerative disease
P1171
Cirak, S.; Klepper, J.; Ballauf, A.; Auth, M.; Voit, T.: Biliary atresia as initial manifestation of Niemann Pick C1 disease
P1172
Vlaho, S.; Posselt, S.; Boda, V.; Baz Bartels, M.; Parbel, S.; Dittrich, S.; Gebhardt, B.; Sewell, A.; Kieslich, M.: A rare progressive neurometabolic disease (L-2-hydroxyglutaric aciduria) diagnosed by urinary organic acid analysis
P1173
Ramantani, G.; Hahn, G.; Hübner, A.; von der Hagen, M.; Ikonomidou, H.: Progressive leucoencephalopathy with macrocephaly, optic atrophy, epileptic seizures, and primary ovarian dysfunction with relative preservation of cognitive functions
P1174
Gaiser, U.; Neuberger, J.; Regel, E.; Emmert, R.; Ries, M.: Pelizaeus Merzbacher phenotype with epilepsy and autosomal recessive inheritance in two siblings