Auflistung Universitätsbibliographie nach Autor "Wolff, Markus"

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Auflistung Universitätsbibliographie nach Autor "Wolff, Markus"

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  • 4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy
    Hedrich, Ulrike B. S.; Lauxmann, Stephan; Wolff, Markus; Synofzik, Matthis; Bast, Thomas; Binelli, Adrian; Serratosa, Jose M.; Martinez-Ulloa, Pedro; Allen, Nicholas M.; King, Mary D.; Gorman, Kathleen M.; Ben Zeev, Bruria; Tzadok, Michal; Wong-Kisiel, Lily; Marjanovic, Dragan; Rubboli, Guido; Sisodiya, Sanjay M.; Lutz, Florian; Ashraf, Harshad Pannikkaveettil; Torge, Kirsten; Yan, Pu; Bosselmann, Christian; Schwarz, Niklas; Fudali, Monika; Lerche, Holger (2021)
  • A multicenter, matched case-control analysis comparing burden-of-illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany
    Strzelczyk, Adam; Schubert-Bast, Susanne; Bast, Thomas; Bettendorf, Ulrich; Fiedler, Barbara; Hamer, Hajo M.; Herting, Arne; Kalski, Malin; Kay, Lara; Kieslich, Matthias; Klein, Karl Martin; Kluger, Gerhard; Kurlemann, Gerhard; Mayer, Thomas; Neubauer, Bernd A.; Polster, Tilman; von Spiczak, Sarah; Stephani, Ulrich; Trollmann, Regina; Wiemer-Kruel, Adelheid; Wolff, Markus; Irwin, John; Carroll, Joe; Pritchard, Clive; Rosenow, Felix (2019)
  • Beneficial impact of high-field intraoperative magnetic resonance imaging on the efficacy of pediatric low-grade glioma surgery
    Roder, Constantin; Breitkopf, Martin; Bisdas, Sotirios; Freitas, Rousinelle da Silva; Dimostheni, Artemisia; Ebinger, Martin; Wolff, Markus; Tatagiba, Marcos; Schuhmann, Martin U. (2016)
  • Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany
    Strzelczyk, Adam; Kalski, Malin; Bast, Thomas; Wiemer-Kruel, Adelheid; Bettendorf, Ulrich; Kay, Lara; Kieslich, Matthias; Kluger, Gerhard; Kurlemann, Gerhard; Mayer, Thomas; Neubauer, Bernd A.; Polster, Tilman; Herting, Arne; von Spiczak, Sarah; Trollmann, Regina; Wolff, Markus; Irwin, John; Carroll, Joe; Macdonald, Daniel; Pritchard, Clive; Klein, Karl Martin; Rosenow, Felix; Schubert-Bast, Susanne (2019)
  • Clinical and imaging findings in children with non-syndromic lambdoid synostosis
    Haas-Lude, K.; Wolff, M.; Will, B.; Bender, B.; Krimmel, M. (2014)
  • Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration
    Belohlavkova, Anezka; Sterbova, Katalin; Betzler, Cornelia; Burkhard, Stuve; Panzer, Axel; Wolff, Markus; Lassuthova, Petra; Vlckova, Marketa; Kyncl, Martin; Benova, Barbora; Jahodova, Alena; Kudr, Martin; Goerg, Maria; Dusek, Petr; Seeman, Pavel; Kluger, Gerhard; Krsek, Pavel (2020)
  • Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies
    Masnada, Silvia; Hedrich, Ulrike B. S.; Gardella, Elena; Schubert, Julian; Kaiwar, Charu; Klee, Eric W.; Lanpher, Brendan C.; Gavrilova, Ralitza H.; Synofzik, Matthis; Bast, Thomas; Gorman, Kathleen; King, Mary D.; Allen, Nicholas M.; Conroy, Judith; Ben Zeev, Bruria; Tzadok, Michal; Korff, Christian; Dubois, Fanny; Ramsey, Keri; Narayanan, Vinodh; Serratosa, Jose M.; Giraldez, Beatriz G.; Helbig, Ingo; Marsh, Eric; O'Brien, Margaret; Bergqvist, Christina A.; Binelli, Adrian; Porter, Brenda; Zaeyen, Eduardo; Horovitz, Dafne D.; Wolff, Markus; Marjanovic, Dragan; Caglayan, Hande S.; Arslan, Mutluay; Pena, Sergio D. J.; Sisodiya, Sanjay M.; Balestrini, Simona; Syrbe, Steffen; Veggiotti, Pierangelo; Lemke, Johannes R.; Moller, Rikke S.; Lerche, Holger; Rubboli, Guido (2017)
  • De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
    Syrbe, Steffen; Hedrich, Ulrike B. S.; Riesch, Erik; Djemie, Tania; Mueller, Stephan; Moller, Rikke S.; Maher, Bridget; Hernandez-Hernandez, Laura; Synofzik, Matthis; Caglayan, Hande S.; Arslan, Mutluay; Serratosa, Jose M.; Nothnagel, Michael; May, Patrick; Krause, Roland; Loeffler, Heidrun; Detert, Katja; Dorn, Thomas; Vogt, Heinrich; Kraemer, Guenter; Schoels, Ludger; Mullis, Primus E.; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Sterbova, Katalin; Craiu, Dana C.; Hoffman-Zacharska, Dorota; Korff, Christian M.; Weber, Yvonne G.; Steinlin, Maja; Gallati, Sabina; Bertsche, Astrid; Bernhard, Matthias K.; Merkenschlager, Andreas; Kiess, Wieland; Gonzalez, Michael; Zuechner, Stephan; Palotie, Aarno; Suls, Arvid; De Jonghe, Peter; Helbig, Ingo; Biskup, Saskia; Wolff, Markus; Maljevic, Snezana; Schule, Rebecca; Sisodiya, Sanjay M.; Weckhuysen, Sarah; Lerche, Holger; Lemke, Johannes R. (2015)
  • Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences
    Biro, Anna; Stephani, Ulrich; Tarallo, Tiziana; Bast, Thomas; Schlachter, Kurt; Fleger, Martin; Kurlemann, Gerhard; Fiedler, Barbara; Leiz, Steffen; Nikanorova, Marina; Wolff, Markus; Mueller, Arnd; Selch, Christina; Staudt, Martin; Kluger, Gerhard (2015)
  • Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial
    Tacke, Moritz; Borggraefe, Ingo; Gerstl, Lucia; Heinen, Florian; Vill, Katharina; Bonfert, Michaela; Bast, Thomas; Neubauer, Bernd Axel; Baumeister, Friedrich; Baethmann, Martina; Bentele, Karl; Blank, Christian; Blank, Harald M.; Bode, Harald; Bosch, Friedrich; Brandl, Ulrich; Brockmann, Knut; Dahlem, Peter; Ernst, Jan-Peter; Feldmann, Evemarie; Fiedler, Andreas; Gerigk, Michael; Hess, Soeren; Hikel, Christiane; Hoffmann, Hans -Georg; Kieslich, Matthias; Klepper, Joerg; Kluger, Gerhard; Koch, Hartmut; Koch, Walter; Korinthenberg, Rudolf; Krois, Ilona; Kuehne, Hermann; Kurlemann, Gerhard; Mandl, Michaela; Mause, Ulrike; Navratil, Peter; Opp, Joachim; Penzien, Johann; Prietsch, Viola; Quattlaender, Axel; Rating, Dietz; Schara, Ulrike; Shamdeen, Mohammed G.; Sprinz, Andreas; Wendker-Magrabi, Hildegard; Stephani, Ulrich; Muhle, Hiltrud; Strassburg, Hans-Michael; Toepke, Baerbel; Trollmann, Regina; Tuschen-Hofstaetter, Elisabeth; Waltz, Stephan; Weber, Gabriele; Wien, Frank U.; Polster, Tilman; Freitag, Hedwig; Soenmez, Otzcam; Reinhardt, Klaus; Traus, Marion; Hoovey, Zeecam; Wolff, Markus (2018)
  • Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
    Wolff, Markus; Johannesen, Katrine M.; Hedrich, Ulrike B. S.; Masnada, Silvia; Rubboli, Guido; Gardella, Elena; Lesca, Gaetan; Ville, Dorothee; Milh, Mathieu; Villard, Laurent; Afenjar, Alexandra; Chantot-Bastaraud, Sandra; Mignot, Cyril; Lardennois, Caroline; Nava, Caroline; Schwarz, Niklas; Gerard, Marion; Perrin, Laurence; Doummar, Diane; Auvin, Stephane; Miranda, Maria J.; Hempel, Maja; Brilstra, Eva; Knoers, Nine; Verbeek, Nienke; van Kempen, Marjan; Braun, Kees P.; Mancini, Grazia; Biskup, Saskia; Hoertnagel, Konstanze; Doecker, Miriam; Bast, Thomas; Loddenkemper, Tobias; Wong-Kisiel, Lily; Baumeister, Friedrich M.; Fazeli, Walid; Striano, Pasquale; Dilena, Robertino; Fontana, Elena; Zara, Federico; Kurlemann, Gerhard; Klepper, Joerg; Thoene, Jess G.; Arndt, Daniel H.; Deconinck, Nicolas; Schmitt-Mechelke, Thomas; Maier, Oliver; Muhle, Hiltrud; Wical, Beverly; Finetti, Claudio; Brueckner, Reinhard; Pietz, Joachim; Golla, Guenther; Jillella, Dinesh; Linnet, Karen M.; Charles, Perrine; Moog, Ute; Oiglane-Shlik, Eve; Mantovani, John F.; Park, Kristen; Deprez, Marie; Lederer, Damien; Mary, Sandrine; Scalais, Emmanuel; Selim, Laila; Van Coster, Rudy; Lagae, Lieven; Nikanorova, Marina; Hjalgrim, Helle; Korenke, G. Christoph; Trivisano, Marina; Specchio, Nicola; Ceulemans, Berten; Dorn, Thomas; Helbig, Katherine L.; Hardies, Katia; Stamberger, Hannah; de Jonghe, Peter; Weckhuysen, Sarah; Lemke, Johannes R.; Kraegeloh-Mann, Ingeborg; Helbig, Ingo; Kluger, Gerhard; Lerche, Holger; Moller, Rikke S. (2017)
  • Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
    Abou-Khalil, Bassel; Auce, Pauls; Avbersek, Andreja; Bahlo, Melanie; Balding, David J.; Bast, Thomas; Baum, Larry; Becker, Albert J.; Becker, Felicitas; Berghuis, Bianca; Berkovic, Samuel F.; Boysen, Katja E.; Bradfield, Jonathan P.; Brody, Lawrence C.; Buono, Russell J.; Campbell, Ellen; Cascino, Gregory D.; Catarino, Claudia B.; Cavalleri, Gianpiero L.; Cherny, Stacey S.; Chinthapalli, Krishna; Coffey, Alison J.; Compston, Alastair; Coppola, Antonietta; Cossette, Patrick; Craig, John J.; de Haan, Gerrit-Jan; De Jonghe, Peter; de Kovel, Carolien G. F.; Delanty, Norman; Depondt, Chantal; Devinsky, Orrin; Dlugos, Dennis J.; Doherty, Colin P.; Elger, Christian E.; Eriksson, Johan G.; Ferraro, Thomas N.; Feucht, Martha; Francis, Ben; Franke, Andre; French, Jacqueline A.; Freytag, Saskia; Gaus, Verena; Geller, Eric B.; Gieger, Christian; Glauser, Tracy; Glynn, Simon; Goldstein, David B.; Gui, Hongsheng; Guo, Youling; Haas, Kevin F.; Hakonarson, Hakon; Hallmann, Kerstin; Haut, Sheryl; Heinzen, Erin L.; Helbig, Ingo; Hengsbach, Christian; Hjalgrim, Helle; Iacomino, Michele; Ingason, Andres; Jamnadas-Khoda, Jennifer; Johnson, Michael R.; Kalviainen, Reetta; Kantanen, Anne-Mari; Kasperaviciute, Dalia; Trenite, Dorothee Kasteleijn-Nolst; Kirsch, Heidi E.; Knowlton, Robert C.; Koeleman, Bobby P. C.; Krause, Roland; Krenn, Martin; Kunz, Wolfram S.; Kuzniecky, Ruben; Kwan, Patrick; Lal, Dennis; Lau, Yu-Lung; Lehesjoki, Anna-Elina; Lerche, Holger; Leu, Costin; Lieb, Wolfgang; Lindhout, Dick; Lo, Warren D.; Lopes-Cendes, Iscia; Lowenstein, Daniel H.; Malovini, Alberto; Marson, Anthony G.; Mayer, Thomas; McCormack, Mark; Mills, James L.; Mirza, Nasir; Moerzinger, Martina; Moller, Rikke S.; Molloy, Anne M.; Muhle, Hiltrud; Newton, Mark; Ng, Ping-Wing; Noethen, Markus M.; Nuernberg, Peter; O'Brien, Terence J.; Oliver, Karen L.; Palotie, Aarno (2018)
  • GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects
    Platzer, Konrad; Yuan, Hongjie; Schuetz, Hannah; Winschel, Alexander; Chen, Wenjuan; Hu, Chun; Kusumoto, Hirofumi; Heyne, Henrike O.; Helbig, Katherine L.; Tang, Sha; Willing, Marcia C.; Tinkle, Brad T.; Adams, Darius J.; Depienne, Christel; Keren, Boris; Mignot, Cyril; Frengen, Eirik; Stromme, Petter; Biskup, Saskia; Doecker, Dennis; Strom, Tim M.; Mefford, Heather C.; Myers, Candace T.; Muir, Alison M.; LaCroix, Amy; Sadleir, Lynette; Scheffer, Ingrid E.; Brilstra, Eva; van Haelst, Mieke M.; van der Smagt, Jasper J.; Bok, Levinus A.; Moller, Rikke S.; Jensen, Uffe B.; Millichap, John J.; Berg, Anne T.; Goldberg, Ethan M.; De Bie, Isabelle; Fox, Stephanie; Major, Philippe; Jones, Julie R.; Zackai, Elaine H.; Abou Jamra, Rami; Rolfs, Arndt; Leventer, Richard J.; Lawson, John A.; Roscioli, Tony; Jansen, Floor E.; Ranza, Emmanuelle; Korff, Christian M.; Lehesjoki, Anna-Elina; Courage, Carolina; Linnankivi, Tarja; Smith, Douglas R.; Stanley, Christine; Mintz, Mark; McKnight, Dianalee; Decker, Amy; Tan, Wen-Hann; Tarnopolsky, Mark A.; Brady, Lauren I.; Wolff, Markus; Dondit, Lutz; Pedro, Helio F.; Parisotto, Sarah E.; Jones, Kelly L.; Patel, Anup D.; Franz, David N.; Vanzo, Rena; Marco, Elysa; Ranells, Judith D.; Di Donato, Nataliya; Dobyns, William B.; Laube, Bodo; Traynelis, Stephen F.; Lemke, Johannes R. (2017)
  • GRIN2B Mutations in West Syndrome and Intellectual Disability with Focal Epilepsy
    Lemke, Johannes R.; Hendrickx, Rik; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Harvey, Robert J.; James, Victoria M.; Pepler, Alex; Steiner, Isabelle; Hoertnagel, Konstanze; Neidhardt, John; Ruf, Susanne; Wolff, Markus; Bartholdi, Deborah; Caraballo, Roberto; Platzer, Konrad; Suls, Arvid; De Jonghe, Peter; Biskup, Saskia; Weckhuysen, Sarah (2014)
  • Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate
    Tzschach, Andreas; Grasshoff, Ute; Schaeferhoff, Karin; Bonin, Michael; Dufke, Andreas; Wolff, Markus; Haas-Lude, Karin; Bevot, Andrea; Riess, Olaf (2012)
  • KCNC1-related disorders: new de novo variants expand the phenotypic spectrum
    Park, Joohyun; Koko, Mahmoud; Hedrich, Ulrike B. S.; Hermann, Andreas; Cremer, Kirsten; Haberlandt, Edda; Grimmel, Mona; Alhaddad, Bader; Beck-Woedl, Stefanie; Harrer, Merle; Karall, Daniela; Kingelhoefer, Lisa; Tzschach, Andreas; Matthies, Lars C.; Strom, Tim M.; Ringelstein, Erich Bernd; Sturm, Marc; Engels, Hartmut; Wolff, Markus; Lerche, Holger; Haack, Tobias B. (2019)
  • Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
    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; Jaehn, Johanna A.; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Moller, Rikke S.; Hjalgrim, Helle; Addis, Laura; Tang, Shan; Hughes, Elaine; Pal, Deb K.; Veri, Kadi; Vaher, Ulvi; Talvik, Tiina; Dimova, Petia; Lopez, Rosa Guerrero; Serratosa, Jose 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, Juergen; Becker, Felicitas; Weber, Yvonne G.; Feucht, Martha; Steinboeck, Hannelore; Neophythou, Birgit; Ronen, Gabriel M.; Gruber-Sedlmayr, Ursula; Geldner, Julia; Harvey, Robert J.; Hoffmann, Per; Herms, Stefan; Altmueller, Janine; Toliat, Mohammad R.; Thiele, Holger; Nuernberg, Peter; Wilhelm, Christian; Stephani, Ulrich; Helbig, Ingo; Lerche, Holger; Zimprich, Fritz; Neubauer, Bernd A.; Biskup, Saskia; von Spiczak, Sarah (2013)
  • Mutations of DEPDC5 cause autosomal dominant focal epilepsies
    Ishida, Saeko; Picard, Fabienne; Rudolf, Gabrielle; Noe, Eric; Achaz, Guillaume; Thomas, Pierre; Genton, Pierre; Mundwiller, Emeline; Wolff, Markus; Marescaux, Christian; Miles, Richard; Baulac, Michel; Hirsch, Edouard; Leguern, Eric; Baulac, Stephanie (2013)
  • On the spacetime mean curvature of surfaces in general relativity
    Wolff, Markus (2023)
  • Parental perception of treatment and medical care in children with craniosynostosis
    Kluba, S.; Rohleder, S.; Wolff, M.; Haas-Lude, K.; Schuhmann, M. U.; Will, B. E.; Reinert, S.; Krimmel, M. (2016)