Auflistung Universitätsbibliographie nach Autor "Ruf, Susanne"

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Auflistung Universitätsbibliographie nach Autor "Ruf, Susanne"

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  • A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability
    Reith, Milda; Zeltner, Lena; Schaeferhoff, Karin; Witt, Dennis; Zuleger, Theresia; Haack, Tobias B.; Bornemann, Antje; Alber, Michael; Ruf, Susanne; Schoels, Ludger; Stingl, Katarina; Weisschuh, Nicole (2022)
  • Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy
    Syrbe, Steffen; Harms, Frederike L.; Parrini, Elena; Montomoli, Martino; Muetze, Ulrike; Helbig, Katherine L.; Polster, Tilman; Albrecht, Beate; Bernbeck, Ulrich; van Binsbergen, Ellen; Biskup, Saskia; Burglen, Lydie; Denecke, Jonas; Heron, Benedicte; Heyne, Henrike O.; Hoffmann, Georg F.; Hornemann, Frauke; Matsushige, Takeshi; Matsuura, Ryuki; Kato, Mitsuhiro; Korenke, G. Christoph; Kuechler, Alma; Laemmer, Constanze; Merkenschlager, Andreas; Mignot, Cyril; Ruf, Susanne; Nakashima, Mitsuko; Saitsu, Hirotomo; Stamberger, Hannah; Pisano, Tiziana; Tohyama, Jun; Weckhuysen, Sarah; Werckx, Wendy; Wickert, Julia; Mari, Francesco; Verbeek, Nienke E.; Moller, Rikke S.; Koeleman, Bobby; Matsumoto, Naomichi; Dobyns, William B.; Battaglia, Domenica; Lemke, Johannes R.; Kutsche, Kerstin; Guerrini, Renzo (2017)
  • Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study
    Grau, Janina; Zollner, Johann Philipp; Schubert-Bast, Susanne; Kurlemann, Gerhard; Hertzberg, Christoph; Wiemer-Kruel, Adelheid; Bast, Thomas; Bertsche, Astrid; Bettendorf, Ulrich; Fiedler, Barbara; Hahn, Andreas; Hartmann, Hans; Hornemann, Frauke; Immisch, Ilka; Jacobs, Julia; Kieslich, Matthias; Klein, Karl Martin; Klotz, Kerstin A.; Kluger, Gerhard; Knuf, Markus; Mayer, Thomas; Marquard, Klaus; Meyer, Sascha; Muhle, Hiltrud; Muller-Schluter, Karen; Noda, Anna H.; Ruf, Susanne; Sauter, Matthias; Schlump, Jan-Ulrich; Syrbe, Steffen; Thiels, Charlotte; Trollmann, Regina; Wilken, Bernd; Willems, Laurent M.; Rosenow, Felix; Strzelczyk, Adam (2021)
  • Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
    Lotte, Jan; Bast, Thomas; Borusiak, Peter; Coppola, Antonietta; Cross, J. Helen; Dimova, Petia; Fogarasi, Andras; Graness, Irene; Guerrini, Renzo; Hjalgrim, Helle; Keimer, Reinhard; Korff, Christian M.; Kurlemann, Gerhard; Leiz, Steffen; Linder-Lucht, Michaela; Loddenkemper, Tobias; Makowski, Christine; Muehe, Christian; Nicolai, Joost; Nikanorova, Marina; Pellacani, Simona; Philip, Sunny; Ruf, Susanne; Fernandez, Ivan Sanchez; Schlachter, Kurt; Striano, Pasquale; Sukhudyan, Biayna; Valcheva, Deyana; Vermeulen, R. Jeroen; Weisbrod, Tanja; Wilken, Bernd; Wolf, Philipp; Kluger, Gerhard (2016)
  • 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)
  • Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from Germany
    Willems, Laurent M.; Schubert-Bast, Susanne; Grau, Janina; Hertzberg, Christoph; Kurlemann, Gerhard; Wiemer-Kruel, Adelheid; Bast, Thomas; Bertsche, Astrid; Bettendorf, Ulrich; Fiedler, Barbara; Hahn, Andreas; Hartmann, Hans; Hornemann, Frauke; Immisch, Ilka; Jacobs, Julia; Kieslich, Matthias; Klein, Karl Martin; Klotz, Kerstin A.; Kluger, Gerhard; Knuf, Markus; Mayer, Thomas; Marquard, Klaus; Meyer, Sascha; Muhle, Hiltrud; Mueller-Schlueter, Karen; Noda, Anna H.; Ruf, Susanne; Sauter, Matthias; Schlump, Jan-Ulrich; Syrbe, Steffen; Thiels, Charlotte; Trollmann, Regina; Wilken, Bernd; Zoellner, Johann Philipp; Rosenow, Felix; Strzelczyk, Adam (2021)
  • Intravenous lacosamide in clinical practice-results from an independent registry
    Lang, Nicolas; Lange, Max; Schmitt, Friedhelm C.; Boes, Monika; Weber, Yvonne; Evers, Stefan; Burghaus, Lothar; Kellinghaus, Christoph; Schubert-Bast, Susanne; Boesel, Julian; Lammers, Thorsten; Sabolek, Michael; van Baalen, Andreas; Dziewas, Rainer; Kraft, Andrea; Ruf, Susanne; Stephani, Ulrich (2016)
  • 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)
  • Prescription patterns of antiseizure drugs in tuberous sclerosis complex (TSC)-associated epilepsy: a multicenter cohort study from Germany and review of the literature
    Strzelczyk, Adam; Grau, Janina; Bast, Thomas; Bertsche, Astrid; Bettendorf, Ulrich; Hahn, Andreas; Hartmann, Hans; Hertzberg, Christoph; Hornemann, Frauke; Immisch, Ilka; Jacobs, Julia; Klotz, Kerstin A.; Kluger, Gerhard; Knake, Susanne; Knuf, Markus; Kurlemann, Gerhard; Marquard, Klaus; Mayer, Thomas; Meyer, Sascha; Muhle, Hiltrud; Mueller-Schlueter, Karen; von Podewils, Felix; Rosenow, Felix; Ruf, Susanne; Sauter, Matthias; Schaefer, Hannah; Schlump, Jan-Ulrich; Schubert-Bast, Susanne; Syrbe, Steffen; Thiels, Charlotte; Trollmann, Regina; Wiemer-Kruel, Adelheid; Wilken, Bernd; Zukunft, Bianca; Zoellner, Johann Philipp (2021)
  • PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures
    Schubert, Julian; Paravidino, Roberta; Becker, Felicitas; Berger, Andrea; Bebek, Nerses; Bianchi, Amedeo; Brockmann, Knut; Capovilla, Giuseppe; Bernardina, Bernardo Dalla; Fukuyama, Yukio; Hoffmann, Georg F.; Jurkat-Rott, Karin; Anttonen, Anna-Kaisa; Kurlemann, Gerhard; Lehesjoki, Anna-Elina; Lehmann-Horn, Frank; Mastrangelo, Massimo; Mause, Ulrike; Mueller, Stephan; Neubauer, Bernd; Puest, Burkhard; Rating, Dietz; Robbiano, Angela; Ruf, Susanne; Schroeder, Christopher; Seidel, Andreas; Specchio, Nicola; Stephani, Ulrich; Striano, Pasquale; Teichler, Jens; Turkdogan, Dilsad; Vigevano, Federico; Viri, Maurizio; Bauer, Peter; Zara, Federico; Lerche, Holger; Weber, Yvonne G. (2012)
  • Report Auditory stimulation during sleep suppresses spike activity in benign epilepsy with centrotemporal spikes
    Klinzing, Jens G.; Tashiro, Lilian; Ruf, Susanne; Wolff, Markus; Born, Jan; Ngo, Hong-Viet V. (2021)
  • SERAC1 deficiency causes complicated HSP: evidence from a novel splice mutation in a large family
    Roeben, Benjamin; Schuele, Rebecca; Ruf, Susanne; Bender, Benjamin; Alhaddad, Bader; Benkert, Tanja; Meitinger, Thomas; Reich, Selina; Boehringer, Judith; Langhans, Claus-Dieter; Vaz, Frederic M.; Wortmann, Saskia B.; Marquardt, Thorsten; Haack, Tobias B.; Kraegeloh-Mann, Ingeborg; Schoels, Ludger; Synofzik, Matthis (2018)
  • Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany
    Maltseva, Margarita; Schubert-Bast, Susanne; Zoellner, Johann Philipp; Bast, Thomas; Mayer, Thomas; von Spiczak, Sarah; Ruf, Susanne; Trollmann, Regina; Wolff, Markus; Hornemann, Frauke; Klotz, Kerstin A.; Jacobs, Julia; Kurlemann, Gerhard; Neubauer, Bernd A.; Polster, Tilman; Syrbe, Steffen; Bertsche, Astrid; Bettendorf, Ulrich; Kluger, Gerhard; Flege, Silke; Rosenow, Felix; Kay, Lara; Strzelczyk, Adam (2023)
  • The phenotypic spectrum of X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy
    Datta, Alexandre N.; Bahi-Buisson, Nadia; Bienvenu, Thierry; Buerki, Sarah E.; Gardiner, Fiona; Cross, J. Helen; Heron, Benedicte; Kaminska, Anna; Korff, Christian M.; Lepine, Anne; Lesca, Gaetan; McTague, Amy; Mefford, Heather C.; Mignot, Cyrill; Milh, Matthieu; Piton, Amelie; Pressler, Ronit M.; Ruf, Susanne; Sadleir, Lynette G.; de Saint Martin, Anne; Van Gassen, Koen; Verbeek, Nienke E.; Ville, Dorothee; Villeneuve, Nathalie; Zacher, Pia; Scheffer, Ingrid E.; Lemke, Johannes R. (2021)