Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Tacke, U

Diagnostics and management of pediatric headaches at a University Hospital

Talmon l'Armée, E

Different courses of Foix-Chavany-Marie syndrome (FCMS) in children with herpes encephalitis

Tappauf, M

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports
Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Tardieu, M

Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings

Tauer, U

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature

Theophil, M

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Thiede, A

Successful therapy with individualized combined speech-and-stutter therapy, psychological motivation, and learning help for an 11-years-old girl with cerebral palsy

Thiele, H

Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders
Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders

Thiels, C

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
Adolescent with neutral lipid storage disease with myopathy caused by a new mutation of the PNPLA2 gene – a dietetic attempt
Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)
Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
Visual impairment – differential diagnoses

Thomale, U

Frontocerebellar tract lesions revealed by tractography in pediatric posterior fossa tumor survivors

Timmermann, L

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Tiranti, V

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation
Exome sequencing in 30 neurodegeneration with brain iron accumulation patients

Toelle, SP

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation

Treumann, T

Primary central nervous system vasculitis in childhood: more frequent and variable than thought

Trippe, H

Alpha-dystroglycanopathies: Clinical and genetic variability
Tetrasomy X and neuropathy: double trouble or extended phenotype?

Trollmann, R

Regenerative neuronal proliferation in hypoxic developing mouse brain is transient and modified by erythropoietin treatment
Interplay of inflammation and hypoxia in perinatal brain injury
Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez
Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants
X-linked Creatine transport deficiency: Phenotypic variability in a family with SLC6A8 gene mutation

Tschiderer, B

Visual disorders in children with cerebral palsy

Tuxhorn, I

A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes

Twilt, M

Pediatric neuromyelitis optica-beyond the optic nerve and spinal cord