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Guipponi, Michel; Chentouf, Amina; Webling, Kristin E.B.; Freimann, Krista; Crespel, Arielle; Nobile, Carlo; Lemke, Johannes R.; Hansen, Jörg; Dorn, Thomas; Lesca, Gaetan; Ryvlin, Philippe; Hirsch, Edouard; Rudolf, Gabrielle; Rosenberg, Dominique Sarah; Weber, Yvonne; Becker, Felicitas; Helbig, Ingo; Muhle, Hiltrud; Salzmann, Annick; Chaouch, Malika; ... (2015). Galanin pathogenic mutations in temporal lobe epilepsy. Human molecular genetics, 24(11), pp. 3082-3091. Oxford University Press 10.1093/hmg/ddv060
Lemke, Johannes R.; Hendrickx, Rik; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Harvey, Robert J.; James, Victoria M.; Pepler, Alex; Steiner, Isabelle; Hörtnagel, Konstanze; Neidhardt, John; Ruf, Susanne; Wolff, Markus; Bartholdi, Deborah; Caraballo, Roberto; Platzer, Konrad; Suls, Arvid; De Jonghe, Peter; Biskup, Saskia and Weckhuysen, Sarah (2014). GRIN2B mutations in west syndrome and intellectual disability with focal epilepsy. Annals of neurology, 75(1), pp. 147-154. Wiley-Blackwell 10.1002/ana.24073
Lemke, Johannes R.; Kernland Lang, Kristin Helene; Hörtnagel, Konstanze; Itin, Peter (2014). Monogenic Human Skin Disorders. Dermatology, 229(2), pp. 55-64. Karger 10.1159/000362200
Kipfer, Stefan; Jung, Simon; Lemke, Johannes R.; Kipfer-Kauer, Anna; Howell, Jeremy P.; Kaelin-Lang, Alain; Nyffeler, Thomas; Gutbrod, Klemens; Abicht, Angela; Müri, René M. (2013). Novel CACNA1A mutation(s) associated with slow saccade velocities. Journal of neurology, 260(12), pp. 3010-3014. Springer Berlin Heidelberg 10.1007/s00415-013-7099-4
