Abstracts of the 37th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Tacke, UH

Infantile epileptic encephalopathy due to cobalamin deficiency?

Tantsis, E

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Tatagiba, M

Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment

Tauer, U

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation

Tegetmeyer, H

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Teig, N

Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II

Tesarova, M

Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Thiele, S

Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Stiff-persons syndrome in a 12 year old child – a case report

Thiels, C

Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics

Thümmler, K

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Tibussek, D

How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey

Toelle, SP

Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?

Trantakis, C

Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus

Triltsch-Ciurea, I

Familiarity and course of specific language impairment of 175 children

Trimmel-Schwahofer, P

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Trollmann, R

Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain
Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales
Isolated optic neuritis is associated with development of pediatric multiple sclerosis

Tuxhorn, I

Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009