Resultados de búsqueda - Philipp S. Reif
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Minocycline as potent anticonvulsant in a patient with astrocytoma and drug resistant epilepsy por Marcin Nowak, Adam Strzelczyk, Philipp S. Reif, Kathrin Schorlemmer, Sebastian Bauer, Braxton A. Norwood, Wolfgang H. Oertel, Felix Rosenow, Herwig Strik, Hajo M. Hamer
Publicado 2012Artigo -
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Sustained seizure remission on perampanel in progressive myoclonic epilepsy (Lafora disease) por Kathrin Schorlemmer, Sebastian Bauer, Marcus Belke, Anke Hermsen, Karl Martin Klein, Philipp S. Reif, Wolfgang H. Oertel, Wolfram S. Kunz, Susanne Knake, Felix Rosenow, Adam Strzelczyk
Publicado 2013Artigo -
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Postmarketing experience with brivaracetam in the treatment of epilepsies: A multicenter cohort study from Germany por Isabel Steinig, Felix von Podewils, Gabriel Möddel, Sebastian Bauer, Karl Martin Klein, Esther Paule, Philipp S. Reif, Laurent M. Willems, Johann Philipp Zöllner, Rhina Kunz, Uwe Runge, Gerhard Kurlemann, Susanne Schubert‐Bast, Felix Rosenow, Adam Strzelczyk
Publicado 2017Artigo -
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Extending the phenotypic spectrum of <i><scp>RBFOX</scp>1</i> deletions: Sporadic focal epilepsy por Dennis Lal, Katharina Pernhorst, Karl Martin Klein, Philipp S. Reif, Rossana Tozzi, Mohammad R. Toliat, Georg Winterer, Bernd A. Neubauer, Peter Nürnberg, Felix Rosenow, Felicitas Becker, Holger Lerche, Wolfram S. Kunz, Mitja Kurki, Per Hoffmann, Albert J. Becker, Emilio Perucca, Federico Zara, Thomas Sander, Yvonne G. Weber
Publicado 2015Artigo -
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Use of brivaracetam in genetic generalized epilepsies and for acute, intravenous treatment of absence status epilepticus por Adam Strzelczyk, Lara Kay, Sebastian Bauer, Ilka Immisch, Karl Martin Klein, Susanne Knake, Alexander B. Kowski, Rhina Kunz, Gerhard Kurlemann, Lisa Langenbruch, Gabriel Möddel, Karen Müller‐Schlüter, Philipp S. Reif, Susanne Schubert‐Bast, Bernhard J. Steinhoff, Isabel Steinig, Laurent M. Willems, Felix von Podewils, Felix Rosenow
Publicado 2018Artigo -
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Efficacy, Retention, and Tolerability of Brivaracetam in Patients With Epileptic Encephalopathies: A Multicenter Cohort Study From Germany por Laurent M. Willems, Astrid Bertsche, Frank Bösebeck, Frauke Hornemann, Ilka Immisch, Karl Martin Klein, Susanne Knake, Rhina Kunz, Gerhard Kurlemann, Lisa Langenbruch, Gabriel Möddel, Karen Müller‐Schlüter, Felix von Podewils, Philipp S. Reif, Bernhard J. Steinhoff, Isabel Steinig, Felix Rosenow, Susanne Schubert‐Bast, Adam Strzelczyk
Publicado 2018Artigo -
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The LaLiMo Trial: lamotrigine compared with levetiracetam in the initial 26 weeks of monotherapy for focal and generalised epilepsy—an open-label, prospective, randomised controlle... por Felix Rosenow, Carmen Schade‐Brittinger, Nicole Burchardi, Sebastian Bauer, Karl Martin Klein, Yvonne G. Weber, Holger Lerche, Stefan Evers, Stjepana Kovac, Susanne Hallmeyer‐Elgner, G. Winkler, Joachim Springub, Mathias Niedhammer, Erhard Roth, Ilonka Eisensehr, Jörg Berrouschot, Stephan Arnold, Michael Schröder, Anja Beige, Wolfgang H. Oertel, Adam Strzelczyk, Anja Haag, Philipp S. Reif, Hajo M. Hamer
Publicado 2012Artigo -
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Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies por Simona Balestrini, Daniela Chiarello, Μαρία Γώγου, Katri Silvennoinen, Clinda Puvirajasinghe, Wendy D. Jones, Philipp S. Reif, Karl Martin Klein, Felix Rosenow, Yvonne G. Weber, Holger Lerche, Susanne Schubert‐Bast, Ingo Borggraefe, Antonietta Coppola, Serena Troisi, Rikke S. Møller, Antonella Riva, Pasquale Striano, Federico Zara, Cheryl Hemingway, Carla Marini, Anna Rosati, Davide Mei, Martino Montomoli, Renzo Guerrini, J. Helen Cross, Sanjay M. Sisodiya
Publicado 2021Artigo -
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Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood por Hannah Stamberger, David Crosiers, Ganna Balagura, Claudia Bonardi, Anna Basu, Gaetano Cantalupo, Valentina Chiesa, Jakob Christensen, Bernardo Dalla Bernardina, Colin A. Ellis, Francesca Furia, Fiona Gardiner, Camille Giron, Renzo Guerrini, Karl Martin Klein, Christian Korff, Hana Krijtová, Melanie Leffler, Holger Lerche, Gaëtan Lesca, David Lewis‐Smith, Carla Marini, Dragan Marjanović, Laure Mazzola, Sarah M. Ruggiero, Fanny Mochel, Francis Ramond, Philipp S. Reif, Aurélie Richard-Mornas, Felix Rosenow, Christian Schropp, Rhys H. Thomas, Aglaia Vignoli, Yvonne G. Weber, Elizabeth E. Palmer, Ingo Helbig, Ingrid E. Scheffer, Pasquale Striano, Rikke S. Møller, Elena Gardella, Sarah Weckhuysen
Publicado 2022Artigo -
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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy por Katherine L. Helbig, Heather C. Mefford, Andrew J. Sharp, Michel Guipponi, Marco Fichera, André Franke, Hiltrud Muhle, Carolien G. F. de Kovel, Carl Baker, Sarah von Spiczak, Katherine L. Kron, Ines Steinich, Ailing A. Kleefuß‐Lie, Costin Leu, Verena Gaus, Bettina Schmitz, Karl Martin Klein, Philipp S. Reif, Felix Rosenow, Yvonne G. Weber, Holger Lerche, Fritz Zimprich, L Urak, Karoline Fuchs, Martha Feucht, Pierre Genton, Pierre Thomas, Frank Visscher, Gerrit‐Jan de Haan, Rikke S. Møller, Helle Hjalgrim, D Luciano, Michael Wittig, Michael Nothnagel, Christian E. Elger, Peter Nürnberg, Corrado Romano, Alain Malafosse, Bobby P.C. Koeleman, Dick Lindhout, Ulrich Stephani, Stefan Schreiber, Evan E. Eichler, Thomas Sander
Publicado 2009Artigo -
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Phenotypic spectrum of <i>GABRA1</i> por Katrine M. Johannesen, Carla Marini, Siona Pfeffer, Rikke S. Møller, Thomas Dorn, Cristina Elena Niturad, Elena Gardella, Yvonne G. Weber, Marianne Søndergård, Helle Hjalgrim, Mariana Nikanorova, Felicitas Becker, Line H.G. Larsen, Hans A. Dahl, Oliver Maier, Davide Mei, Saskia Biskup, Karl Martin Klein, Philipp S. Reif, Felix Rosenow, Abdallah F. Elias, Cindy Hudson, Katherine L. Helbig, Susanne Schubert‐Bast, Maria Rosaria Scordo, Dana Craiu, Tania Djémié, Dorota Hoffman‐Zacharska, Hande Çağlayan, Ingo Helbig, José M. Serratosa, Pasquale Striano, Peter De Jonghe, Sarah Weckhuysen, Arvid Suls, Kai Muru, Inga Talvik, Tiina Talvik, Hiltrud Muhle, Ingo Borggraefe, Imma Rost, Renzo Guerrini, Holger Lerche, Johannes R. Lemke, Guido Rubboli, Snezana Maljevic
Publicado 2016Artigo -
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From theory to practice: Critical points in the 2017 ILAE classification of epileptic seizures and epilepsies por André Palmini, Naoki Akamatsu, Thomas Bast, Sebastian Bauer, Christoph Baumgartner, Selim R. Benbadis, Adriana Bermeo‐Ovalle, Stefan Beyenburg, Andrew Bleasel, Alireza Bozorgi, Milan Brázdil, Mar Carreño, Norman Delanty, Michael W. Devereaux, John S. Duncan, Guadalupe Fernández‐Baca Vaca, Naiara García Losarcos, Lauren Ghanma, António Gil‐Nagel, Hajo M. Hamer, Hans Holthausen, Shirin Jamal Omidi, Philippe Kahane, Giridhar P. Kalamangalam, Andrés M. Kanner, Susanne Knake, Stjepana Kovac, Guenter Kraemer, Gerhard Kurlemann, Nuria Lacuey, Patrick Landazuri, Shih Hui Lim, Giorgio Lo Russo, Hans O. Lüders, Jayanti Mani, Riki Matsumoto, Jonathan Miller, Soheyl Noachtar, Rebecca O’Dwyer, Jun Park, Philipp S. Reif, Jan Rémi, Felix Rosenow, Américo Ceiki Sakamoto, Susanne Schubert‐Bast, Stephan Schuele, Asim Shahid, J. Bernhard Steinhoff, Adam Strzelczyk, C. Ákos Szabó, Nitin Tandon, Kiyohito Terada, Manuel Toledo, W. van Emde Boas, Matthew C. Walker, Peter Widdess‐Walsh
Publicado 2020Carta -
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Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new “Integrated Epilepsy Classification”? por Felix Rosenow, Naoki Akamatsu, Thomas Bast, Sebastian Bauer, Christoph Baumgartner, Selim R. Benbadis, Adriana Bermeo‐Ovalle, Stefan Beyenburg, Andrew Bleasel, Alireza Bozorgi, Milan Brázdil, Mar Carreño, Norman Delanty, Michael W. Devereaux, John S. Duncan, Guadalupe Fernández‐Baca Vaca, Stefano Francione, Naiara García Losarcos, Lauren Ghanma, António Gil‐Nagel, Hajo M. Hamer, Hans Holthausen, Shirin Jamal Omidi, Philippe Kahane, Giridhar P. Kalamangalam, Andrés M. Kanner, Susanne Knake, Stjepana Kovac, Karsten Krakow, Günter Krämer, Gerhard Kurlemann, Nuria Lacuey, Patrick Landazuri, Shi Hui Lim, Luisa V. Londoño, Giorgio Lo Russo, Hans O. Lüders, Jayanti Mani, Riki Matsumoto, Jonathan Miller, Soheyl Noachtar, Rebecca O’Dwyer, André Palmini, Jun Park, Philipp S. Reif, Jan Rémi, Américo Ceiki Sakamoto, Bettina Schmitz, Susanne Schubert‐Bast, Stephan Schuele, Asim Shahid, Bernhard J. Steinhoff, Adam Strzelczyk, C. Ákos Szabó, Nitin Tandon, Kiyohito Terada, Manuel Toledo, W. van Emde Boas, Matthew C. Walker, Peter Widdess‐Walsh
Publicado 2020Revisão -
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Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 por Rahel T. Florian, Florian Kraft, Elsa Leitão, Sabine Kaya, Stephan Klebe, Éloi Magnin, Anne‐Fleur van Rootselaar, Julien Buratti, Theresa Kühnel, Christopher Schröder, Sebastian Gießelmann, Nikolai Tschernoster, Janine Altmueller, Anaide Lamiral, Boris Keren, Caroline Nava, Delphine Bouteiller, Sylvie Forlani, Ludmila Jornéa, Regina Kubica, Tao Ye, Damien Plassard, Bernard Jost, Vincent Meyer, Jean‐François Deleuze, Yannick Delpu, Mario Davide Maria Avarello, Lisanne S. Vijfhuizen, Gabrielle Rudolf, Édouard Hirsch, Thessa Kroes, Philipp S. Reif, Felix Rosenow, Christos Ganos, Marie Vidailhet, Lionel Thivard, Alexandre Mathieu, Thomas Bourgeron, Ingo Kurth, Haloom Rafehi, Laura Steenpaß, Bernhard Horsthemke, Samuel F. Berkovic, Francesca Bisulli, Francesco Brancati, Laura Canafoglia, Giorgio Casari, Renzo Guerrini, Hiroyuki Ishiura, Laura Licchetta, Davide Mei, Tommaso Pippucci, Lynette G. Sadleir, Ingrid E. Scheffer, Pasquale Striano, Paolo Tinuper, Shoji Tsuji, Federico Zara, Eric LeGuern, Karl Martin Klein, Pierre Labauge, Mark F. Bennett, Melanie Bahlo, Jozef Gécz, Mark Corbett, Marina A.J. Tijssen, Arn M. J. M. van den Maagdenberg, Christel Depienne
Publicado 2019Artigo -
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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A por Dalia Kasperavičiūtė, Claudia B. Catarino, Mar Matarín, Costin Leu, Jan Nový, Anna Tostevin, Bárbara Leal, Ellen V.S. Hessel, Kerstin Hallmann, Michael S. Hildebrand, Hans‐Henrik M. Dahl, Mina Ryten, Daniah Trabzuni, Adaikalavan Ramasamy, Saud Alhusaini, Colin P. Doherty, Thomas Dorn, Jörg Hansen, Günter Krämer, Bernhard J. Steinhoff, Dominik Zumsteg, Susan Duncan, Reetta Kälviäinen, Kai Eriksson, Anne-Mari Kantanen, Massimo Pandolfo, U Gruber‐Sedlmayr, Kurt Schlachter, Eva M. Reinthaler, Elisabeth Stögmann, Fritz Zimprich, Emilie Théâtre, Colin Smith, Terence J. O’Brien, K. Meng Tan, Slavé Petrovski, Angela Robbiano, Roberta Paravidino, Federico Zara, Pasquale Striano, Michael R. Sperling, Russell J. Buono, Hákon Hákonarson, João Chaves, Paulo Costa, Berta Martins da Silva, António Martins da Silva, P.N.E. de Graan, Bobby P.C. Koeleman, Albert J. Becker, Susanne Schoch, Marec von Lehe, Philipp S. Reif, Felix Rosenow, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Karl Rössler, Michael Buchfelder, Hajo M. Hamer, Katja Kobow, Roland Coras, Ingmar Blümcke, Ingrid E. Scheffer, Samuel F. Berkovic, Michael E. Weale, Norman Delanty, Chantal Depondt, Gianpiero L. Cavalleri, Wolfram S. Kunz, Sanjay M. Sisodiya
Publicado 2013Revisão -
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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 por Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert, Federico Zara, Pasquale Striano, Angela Robbiano, Giuseppe Capovilla, Paolo Tinuper, Antonio Gambardella, Amedeo Bianchi, Angela La Neve, Giovanni Crichiutti, Carolien G. F. de Kovel, Dorothee Kasteleijn‐Nolst Trenité, Gerrit‐Jan de Haan, Dick Lindhout, Verena Gaus, Bettina Schmitz, Diéter Janz, Yvonne G. Weber, Felicitas Becker, Holger Lerche, Bernhard J. Steinhoff, Ailing A. Kleefuß‐Lie, Wolfram S. Kunz, Rainer Surges, Christian E. Elger, Hiltrud Muhle, Sarah von Spiczak, P Ostertag, Ingo Helbig, Ulrich Stephani, Rikke S. Møller, Helle Hjalgrim, Leanne M. Dibbens, Susannah T. Bellows, Karen Oliver, Saul A. Mullen, Ingrid E. Scheffer, Samuel F. Berkovic, Kate V. Everett, M. R. Gardiner, Carla Marini, Renzo Guerrini, Anna‐Elina Lehesjoki, Auli Sirén, Michel Guipponi, Alain Malafosse, Pierre Thomas, Rima Nabbout, Stéphanie Baulac, Eric LeGuern, Rosa Guerrero, José M. Serratosa, Philipp S. Reif, Felix Rosenow, Martina Mörzinger, Martha Feucht, Fritz Zimprich, Claudia Kapser, Christoph J. Schankin, Arvid Suls, Kaat Smets, Peter De Jonghe, Albena Jordanova, Hande Çağlayan, Zühal Yapıcı, Demet Yalcin, Betül Baykan, Nerses Bebek, Uğur Özbek, Christian Gieger, H.‐Erich Wichmann, Tobias Balschun, David Ellinghaus, André Franke, Christian Meesters, Tim Becker, T. F. Wienker, Anne Hempelmann, Herbert Schulz, Franz Rüschendorf, Markus Leber, S. M. Pauck, Holger Trucks, Mohammad-Reza Toliat, Peter Nürnberg, G. Avanzini, Bobby P.C. Koeleman, T. Sander
Publicado 2012Artigo -
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NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns por Hannah Stamberger, Trine Bjørg Hammer, Elena Gardella, Danique R.M. Vlaskamp, Birgitte Bertelsen, Simone Mandelstam, Iris Lange, Jing Zhang, Candace T. Myers, Christina Fenger, Zaid Afawi, Edith P. Almanza Fuerte, Danielle M. Andrade, Yunus Balcik, Bruria Ben Zeev, Mark F. Bennett, Samuel F. Berkovic, Bertrand Isidor, Arjan Bouman, Eva H. Brilstra, Øyvind L. Busk, Anita Cairns, Roseline Caumes, Nicolas Chatron, Russell C. Dale, Christa de Geus, Patrick Edery, Deepak Gill, Jacob Bie Granild-Jensen, Lauren Gunderson, Boudewijn Gunning, Gali Heimer, Johan Robert Helle, Michael S. Hildebrand, Georgie Hollingsworth, Volodymyr Kharytonov, Eric W. Klee, Bobby P.C. Koeleman, David A. Koolen, Christian Korff, Sébastien Küry, Gaëtan Lesca, Dorit Lev, Richard J. Leventer, Mark T. Mackay, Erica L. Macke, Meriel McEntagart, Shekeeb S. Mohammad, Pauline Monin, Martino Montomoli, Éva Morava, Sébastien Moutton, Alison M. Muir, Elena Parrini, Peter Procopis, Emmanuelle Ranza, Laura Reed, Philipp S. Reif, Felix Rosenow, Massimiliano Rossi, Lynette G. Sadleir, Tara Sadoway, Helenius J. Schelhaas, Amy L. Schneider, Krati Shah, Ruth S. Shalev, Sanjay M. Sisodiya, Thomas Smol, Connie T. R. M. Stumpel, Kyra E. Stuurman, Joseph D. Symonds, Frédéric Tran Mau‐Them, Nienke E. Verbeek, Judith Verhoeven, Geoff Wallace, Keren Yosovich, Yuri A. Zárate, Ayelet Zerem, Sameer M. Zuberi, Renzo Guerrini, Heather C. Mefford, Chirag Patel, Yue-Hua Zhang, Rikke S. Møller, Ingrid E. Scheffer
Publicado 2020Artigo -
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16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy por Eva M. Reinthaler, Dennis Lal, Sébastien Lebon, Michael S. Hildebrand, Hans‐Henrik M. Dahl, Brigid M. Regan, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Gabriel M. Ronen, Laurian Roche, U Gruber‐Sedlmayr, Julia Geldner, Edda Haberlandt, Per Hoffmann, Stefan Herms, Christian Gieger, Mélanie Waldenberger, André Franke, Michael Wittig, Susanne Schoch, Albert J. Becker, Andreas Hahn, Katrin Männik, Mohammad R. Toliat, Georg Winterer, Holger Lerche, Peter Nürnberg, Heather C. Mefford, Ingrid E. Scheffer, Samuel F. Berkovic, J. Beckmann, Thomas Sander, Sébastien Jacquemont, Alexandre Reymond, Fritz Zimprich, Bernd A. Neubauer, Eva M. Reinthaler, Fritz Zimprich, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Julia Geldner, U Gruber‐Sedlmayr, Edda Haberlandt, Gabriel M. Ronen, Laurian Roche, Dennis Lal, Peter Nürnberg, Thomas Sander, Holger Lerche, Bernd A. Neubauer, Fritz Zimprich, Martina Mörzinger, Martha Feucht, Arvid Suls, Sarah Weckhuysen, Lieve Claes, Liesbet Deprez, Katrien Smets, Tine Van Dyck, Tine Deconinck, Peter De Jonghe, Rikke S. Møller, Laura L. Klitten, Helle Hjalgrim, Rikke S. Møller, Kiel Campus, Ingo Helbig, Hiltrud Muhle, P Ostertag, Sarah von Spiczak, Ulrich Stephani, Peter Nürnberg, Thomas Sander, Holger Trucks, Christian E. Elger, Ailing A. Kleefuß‐Lie, Wolfram S. Kunz, Rainer Surges, Verena Gaus, Diéter Janz, Thomas Sander, Bettina Schmitz, Felix Rosenow, Karl Martin Klein, Philipp S. Reif, Wolfgang H. Oertel, Hajo M. Hamer, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Bobby P.C. Koeleman, Carolien G. F. de Kovel, Dick Lindhout, Dick Lindhout, Agnès Ameil, Joris Andrieux, Sonia Bouquillon, Odile Boute
Publicado 2014Artigo
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