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

Abstracts (HTML) Autorenliste

Zabel, B

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

Zanni, G

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Zaugg, C

Dopamine-responsive dystonia: Clinical and therapeutic variability with identical genetic defect

Zebedin, D

Tuberous sclerosis complex-successful therapy with everolimus

Zeches-Kánsy, C

Characteristic MRI finding in severe tick-borne encephalitis in children and the effect of immunoglobulin G on the course of the disease

Zeiner, F

Cardiomyopathy in a patient with Mb Duchenne first presenting as myocardial infarction in childhood

Zellner, A

Lacosamide in childhood-results of a retrospective analysis

Zenz, W

Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?

Zernikow, B

Quantitative sensory testing in children and adolescents with tension type headache: changes in nociceptive processing are not specific for migraine

Zerres, K

Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Zeschnigk, C

Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations

Zimmerhackl, LB

Lyme neuroborreliosis: aetiology and diagnosis of facial palsy in children from Tyrol

Zimmermann, F

Clinical symptoms of six children with thiamin pyrophosphokinase deficiency

Zirn, S

Central or combined central and peripheral hearing loss at an early born child

Zotter, S

Neuropsychological long-term outcome in children with SVT
Epileptic seizures and chromosomal microdeletions/duplications
Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Zschocke, J

Epileptic seizures and chromosomal microdeletions/duplications
Familial occurrence of a 16p13 microdeletion including GRIN2A as a cause of developmental delay and epilepsy with continuous spike and waves during sleep

Zweier, C

Nicolaides-Baraitser Syndrome