Elisabeth Stogmann
Department of Clinical Neurology
Medical University of Vienna
Waehringer Guertel 18-20
A-1090 Vienna
Austria
Name/email consistency: high
- Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Stogmann, E., Reinthaler, E., Eltawil, S., El Etribi, M.A., Hemeda, M., El Nahhas, N., Gaber, A.M., Fouad, A., Edris, S., Benet-Pages, A., Eck, S.H., Pataraia, E., Mei, D., Brice, A., Lesage, S., Guerrini, R., Zimprich, F., Strom, T.M., Zimprich, A. Brain (2013)
- A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. Stogmann, E., El Tawil, S., Wagenstaller, J., Gaber, A., Edris, S., Abdelhady, A., Assem-Hilger, E., Leutmezer, F., Bonelli, S., Baumgartner, C., Zimprich, F., Strom, T.M., Zimprich, A. Neurogenetics (2009)
- Lack of association between a GABA receptor 1 gene polymorphism and temporal lobe epilepsy. Stogmann, E., Zimprich, A., Baumgartner, C., Gleiss, A., Zimprich, F. Epilepsia (2006)