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

Abstracts (HTML) List of Authors

Nagel, B

Tuberous sclerosis complex-successful therapy with everolimus

Nägele, T

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Neef, J

Panic attacks in girls with double cortex syndrome: ictal amaurosis

Neininger, MP

Ambulatory follow-up care of children treated with anticonvulsants and knowledge of parents regarding emergency treatment and safety precautions

Neubauer, BA

Mutation analysis of KCNAB1 in rolandic epilepsy
A double-blinded, randomized, head-to-head trial of levetiracetam versus sulthiame in benign epilepsy with centrotemporal spikes
Linear scleroderma en coup de sabre – two case reports with inflammatory CNS lesions

Neubert, G

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Nguyen-Minh, S

A large homozygous microdeletion in the RAB3GAP1 gene causes Warburg Micro syndrome

Ninnemann, O

Effects of CDK5RAP2 downregulation in murine embryonic stem cells correlate with cellular phenotype in MCPH3 patients

Nissen, C

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Noachtar, S

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

Nolte, K

Central nervous system demyelination complicating Guillain-Barré syndrome
Neurometabolic changes in patients with subacute sclerosing panencephalitis

Normann, C

Influence of lovastatin on synaptic plasticity and fear conditioning in humans with in BDNF val/met genotype

Novak, A

Quality of life and mental health of neuropediatric patients

Novotná, B

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Nürnberg, P

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