Abstracts of the 36th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Abdul-Khaliq, H

The role of EEG in monitoring cerebral dysfunction before and after cardiac surgery in children congenital heart disease

Abels, C

Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
Narcolepsy in early childhood – a case study with video
First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood

Acquaviva, C

Neonatal hypotonia with burst suppression pattern reveals non ketotic hyperglycinemia associated with P-protein deficiency

Ae Lee-Kirsch, M

Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases

Aksu, F

The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults
Quantitative Sensory Testing in children and adolescents with cerebral palsy
Developmental and sex differences of somatosensory perception

Alber, M

Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis

Althaus, J

Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
Hypothalamic and pituitary affection after traumatic brain injury in childhood
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis

Arnold, M

Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke

Assmann, B

„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls
Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved
Use of guidelines improves the neurological outcome in glutaric aciduria type I

Auber, B

FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers

Axer, S

MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case