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- TP1 Genome-wide association analysis and gene identification in migraine with aura
- TP2 Whole-genome association study in migraine without aura and functional characterization of disease associated alleles
- TP3 Genome-wide association mapping of gene configurations conferring risk to idiopathic generalized epilepsies
- TP4 High-throughput sequencing of functional and positional candidate genes for common forms of migraine and epilepsy
- TP5 Genetic basis of Levetiracetam pharmacoresistance and side effects in human epilepsy
- TP6 Functional analysis of human ion channel mutations in cellular and animal models
- TP7 Aberrant transcriptional networks in human epileptic tissue
- TP8 Mechanisms underlying the development of cellular hyperexcitability in mouse models of human epilepsy
- TP9 Subthreshold ion channels in epileptogenesis and neuronal synchronization
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