Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Tacke, U.

Wernicke encephalopathy in childhood

Taeuber, A.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Telegravciska, M.

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Tesarova, M.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Thoms, K.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Timmann-Braun, D.

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Tinschert, S.

Pontine tegmental cap dysplasia: Two additional cases
Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Trefz, F. K.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

Trimmel-Schwahofer, P.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Tro-Baumann, B.

Provocation of seizures by vaccination with children suffering from SCN1A-mutation

Trollmann, R.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report
Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Tsiakas, K.

Treatment of NPC with miglustat in Germany
Manifestation and diagnosis of NPC disease in Germany

Tuglaci, S.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Turski, L.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Tyshchenko, N.

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report