Entries of Smitka, Martin on the publication server

Sell, Katharina, Storch, Katja, Hahn, Gabriele, Lee-Kirsch, Min Ae, Ramantani, Georgia , Jackson, Sandra, Neilson, Derek, von der Hagen, Maja, Hehr, Ute and Smitka, Martin (2016) Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation. Brain and Development 38 (8), pp. 777-780. Fulltext not available.

Heussinger, Nicole, Kontopantelis, Evangelos , Gburek‐Augustat, Janina, Jenke, Andreas, Vollrath, Gesa, Korinthenberg, Rudolf , Hofstetter, Peter, Meyer, Sascha, Brecht, Isabel, Kornek, Barbara, Herkenrath, Peter, Schimmel, Mareike, Wenner, Kirsten, Häusler, Martin, Lutz, Soeren, Karenfort, Michael, Blaschek, Astrid, Smitka, Martin, Karch, Stephanie, Piepkorn, Martin, Rostasy, Kevin, Lücke, Thomas, Weber, Peter, Trollmann, Regina, Klepper, Jörg, Häussler, Martin, Hofmann, Regina, Weissert, Robert , Merkenschlager, Andreas and Buttmann, Mathias (2015) Oligoclonal bands predict multiple sclerosis in children with optic neuritis. Annals of Neurology 77 (6), pp. 1076-1082. Fulltext not available.

Yis, Uluc, Uyanik, Gökhan, Heck, Pinar Bambul, Smitka, Martin, Nobel, Hannes, Ebinger, Friedrich, Dirik, Eray, Feng, Lucy, Kurul, Semra H., Brocke, Katja, Unalp, Aycan, Özer, Erdener, Cakmakci, Handan, Sewry, Caroline, Cirak, Sebahattin, Muntoni, Francesco, Hehr, Ute and Morris-Rosendahl, Deborah J. (2011) Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: Less severe mutations predominate in patients with a non-Walker-Warburg phenotype. Neuromuscular Disorders 21 (1), pp. 20-30. Fulltext not available.