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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Elisabeth Stogmann

Department of Clinical Neurology

Medical University of Vienna

Waehringer Guertel 18-20

A-1090 Vienna

Austria

[email]@meduniwien.ac.at

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Clinical Neurology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. 2006 - 2013

References

  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
 
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