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Number of items: 10.

Papuc, Sorina M; Abela, Lucia; Steindl, Katharina; Begemann, Anaïs; Simmons, Thomas L; Schmitt, Bernhard; Zweier, Markus; Oneda, Beatrice; Socher, Eileen; Crowther, Lisa M; Wohlrab, Gabriele; Gogoll, Laura; Poms, Martin; Seiler, Michelle; Papik, Michael; Baldinger, Rosa; Baumer, Alessandra; Asadollahi, Reza; Kroell-Seger, Judith; Schmid, Regula; Iff, Tobias; Schmitt-Mechelke, Thomas; Otten, Karoline; Hackenberg, Annette; Addor, Marie-Claude; Klein, Andrea; Azzarello-Burri, Silvia; Sticht, Heinrich; Joset, Pascal; Plecko, Barbara; Rauch, Anita (2019). The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study. European Journal of Human Genetics, 27(3):408-421.

Kurian, Mary; Korff, Christian M; Ranza, Emmanuelle; Bernasconi, Andrea; Lübbig, Anja; Nangia, Srishti; Ramelli, Gian Paolo; Wohlrab, Gabriele; Nordli, Douglas R; Bast, Thomas (2018). Focal cortical malformations in children with early infantile epilepsy and PCDH19 mutations: case report. Developmental Medicine and Child Neurology, 60(1):100-105.

Wiemer-Kruel, Adelheid; Haberlandt, Edda; Hartmann, Hans; Wohlrab, Gabriele; Bast, Thomas (2017). Modified Atkins diet is an effective treatment for children with Doose syndrome. Epilepsia, 58(4):657-662.

Latal, Beatrice; Wohlrab, Gabriele; Brotschi, Barbara; Beck, Ingrid; Knirsch, Walter; Bernet, Vera (2016). Postoperative amplitude-integrated electroencephalography predicts four-year neurodevelopmental outcome in children with complex congenital heart disease. Journal of Pediatrics, 178:55-60.

Tibussek, Daniel; Klepper, Jörg; Korinthenberg, Rudolf; Kurlemann, Gerhard; Rating, Dietz; Wohlrab, Gabriele; Wolff, Markus; Schmitt, Bernhard (2016). Treatment of infantile spasms: report of the interdisciplinary guideline committee coordinated by the german-speaking Society for Neuropediatrics. Neuropediatrics, 47(3):139-150.

Wohlrab, Gabriele; Hackenberg, Annette (2016). Neonatale Anfälle und ihre Behandlung. Epileptologie, 33(2):86-94.

Padden, Beth; Scheer, Ianina; Brotschi, Barbara; Wohlrab, Gabriele; Latal, Beatrice; Bernet, Vera (2015). Does amplitude-integrated electroencephalogram background pattern correlate with cerebral injury in neonates with hypoxic-ischaemic encephalopathy? Journal of Paediatrics and Child Health, 51(2):180-185.

Riikonen, Raili; Rener-Primec, Zvonka; Carmant, Lionel; Dorofeeva, Maria; Hollody, Katalin; Szabo, Ilona; Krajnc, Branka S; Wohlrab, Gabriele; Sorri, Iiris (2015). Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study. Developmental Medicine and Child Neurology, 57(1):60-67.

Lemke, Johannes R; Lal, Dennis; Reinthaler, Eva M; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jähn, Johanna A; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Møller, Rikke S; Hjalgrim, Helle; Addis, Laura; Tang, Shan; Hughes, Elaine; Pal, Deb K; Veri, Kadi; Vaher, Ulvi; Talvik, Tiina; Dimova, Petia; Guerrero López, Rosa; Serratosa, José M; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Ruf, Susanne; Wolff, Markus; Buerki, Sarah; Wohlrab, Gabriele; Kroell, Judith; Datta, Alexandre N; Fiedler, Barbara; Kurlemann, Gerhard; Kluger, Gerhard; Hahn, Andreas; Haberlandt, D Edda; Kutzer, Christina; Sperner, Jürgen; Becker, Felicitas; Weber, Yvonne G; Feucht, Martha; Steinböck, Hannelore; Neophythou, Birgit; Ronen, Gabriel M; Gruber-Sedlmayr, Ursula; Geldner, Julia; Harvey, Robert J; Hoffmann, Per; Herms, Stefan; Altmüller, Janine; Toliat, Mohammad R; Thiele, Holger; Nürnberg, Peter; Wilhelm, Christian; Stephani, Ulrich; Helbig, Ingo; Lerche, Holger; Zimprich, Fritz; Neubauer, Bernd A; Biskup, Saskia; von Spiczak, Sarah (2013). Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature Genetics, 45(9):1067-1072.

Wohlrab, Gabriele; et al; Hehr, Ute; Schmitt, Bernhard; Boltshauser, Eugen (2005). Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation. European Journal of Pediatrics, 164(5):326-328.

This list was generated on Wed Sep 18 05:22:12 2019 CEST.