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

Abstracts (HTML) List of Authors

Christen, HJ

Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved

Clarke, NF

Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene

Classen, G

MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Autosomal dominant nocturnal frontal lobe epilepsy in mother and daughter treated with an unusual combination of anticonvulsants
Ketogenic diet in children with difficult to treat epilepsies – 6 years of clinical experience

Coker, M

Towards the genetic defect in MEGDEL syndrome: Four novel patients

Connelly, A

Microstructural alterations of motor pathways in adolescents born preterm

Coropceanu, D

EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus