Search Results - Markus Wolff

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  1. 1
    Phenotypic spectrum and genetics of <i> <scp>SCN</scp> 2A </i> ‐related disorders, treatment options, and outcomes in epilepsy and beyond

    Phenotypic spectrum and genetics of <i> <scp>SCN</scp> 2A </i> ‐related disorders, treatment options, and outcomes in epilepsy and beyond by Markus Wolff, Andreas Brunklaus, Sameer M. Zuberi

    Published 2019
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  2. 2
    Penetration of ciprofloxacin into cerebrospinal fluid of patients with bacterial meningitis

    Penetration of ciprofloxacin into cerebrospinal fluid of patients with bacterial meningitis by Markus Wolff, L Boutron, E Singlas, Bernard Clair, J.M. Decazes, B. Régnier

    Published 1987
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  3. 3
    Benign Partial Epilepsy in Childhood: Selective Cognitive Deficits Are Related to the Location of Focal Spikes Determined by Combined EEG/MEG

    Benign Partial Epilepsy in Childhood: Selective Cognitive Deficits Are Related to the Location of Focal Spikes Determined by Combined EEG/MEG by Markus Wolff, Nikolaus Weiskopf, Emilio Serra, Hubert Preißl, Niels Birbaumer, Ingeborg Krägeloh‐Mann

    Published 2005
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  4. 4
    Analgesic Efficacy and Safety of an Intraoral Lidocaine Patch

    Analgesic Efficacy and Safety of an Intraoral Lidocaine Patch by Elliot V. Hersh, MILTON I. HOUPT, Stephen A. Cooper, Roy S. Feldman, Markus Wolff, Lawrence M. Levin

    Published 1996
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  5. 5
    Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics

    Treatment of Infantile Spasm Syndrome: Update from the Interdisciplinary Guideline Committee Coordinated by the German-Speaking Society of Neuropediatrics by Georgia Ramantani, Bigna K. Bölsterli, Michael Alber, Joerg Klepper, Rudolf Korinthenberg, Gerhard Kurlemann, Daniel Tibussek, Markus Wolff, Bernhard Schmitt

    Published 2022
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  6. 6
    Beneficial impact of high-field intraoperative magnetic resonance imaging on the efficacy of pediatric low-grade glioma surgery

    Beneficial impact of high-field intraoperative magnetic resonance imaging on the efficacy of pediatric low-grade glioma surgery by Constantin Roder, Martin Breitkopf, MS MS, Sotirios Bisdas, Rousinelle da Silva Freitas, Artemisia Dimostheni, Martin Ebinger, Markus Wolff, Marcos Tatagiba, Martin U. Schuhmann

    Published 2016
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  7. 7
    In utero antiepileptic drug exposure

    In utero antiepileptic drug exposure by Kimford J. Meador, Gus A. Baker, Richard H. Finnell, Laura A. Kalayjian, Joyce Liporace, David W. Loring, G. E. Mawer, Page B. Pennell, J. CAMPBELL SMITH, Markus Wolff

    Published 2006
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  8. 8
    Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences

    Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences by Ulrich Stephani, Tiziana Tarallo, Thomas Bast, Kurt Schlachter, Martin Fleger, Gerhard Kurlemann, Barbara Fiedler, Steffen Leiz, Marina Nikanorova, Markus Wolff, Arnd Müller, C. Selch, Martin Staudt, Gerhard Kluger, A Biró

    Published 2015
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  9. 9
    Mutations of DEPDC5 cause autosomal dominant focal epilepsies

    Mutations of DEPDC5 cause autosomal dominant focal epilepsies by Saeko Ishida, Fabienne Picard, Gabrielle Rudolf, Eric Noé, Guillaume Achaz, Pierre Thomas, Pierre Genton, Emeline Mundwiller, Markus Wolff, Christian Marescaux, Richard Miles, Michel Baulac, Édouard Hirsch, Eric LeGuern, Stéphanie Baulac

    Published 2013
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  10. 10
    Functional correlates of clinical phenotype and severity in recurrent SCN2A variants

    Functional correlates of clinical phenotype and severity in recurrent SCN2A variants by Géza Berecki, Katherine B. Howell, Jacqueline Heighway, N.B. Olivier, Jill Rodda, Isabella Overmars, Danique R.M. Vlaskamp, Tyson L. Ware, Simone Ardern‐Holmes, Gaëtan Lesca, Michael Alber, Pierangelo Veggiotti, Ingrid E. Scheffer, Samuel F. Berkovic, Markus Wolff, Steven Petrou

    Published 2022
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  11. 11
    <i>GRIN2B</i> mutations in west syndrome and intellectual disability with focal epilepsy

    <i>GRIN2B</i> mutations in west syndrome and intellectual disability with focal epilepsy by Johannes R. Lemke, Rik Hendrickx, Kirsten Geider, Bodo Laube, Michael Schwake, Victoria L. Harvey, Victoria M. James, Alex Pepler, Isabelle Steiner, Konstanze Hörtnagel, John Neidhardt, Susanne Ruf, Markus Wolff, Deborah Bartholdi, Roberto Caraballo, Konrad Platzer, Arvid Suls, Peter De Jonghe, Saskia Biskup, Sarah Weckhuysen

    Published 2013
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  12. 12
    <i>KCNC1</i>‐related disorders: new de novo variants expand the phenotypic spectrum

    <i>KCNC1</i>‐related disorders: new de novo variants expand the phenotypic spectrum by Joohyun Park, Mahmoud Koko, Ulrike B. S. Hedrich, Andreas Hermann, Kirsten Cremer, Edda Haberlandt, Mona Grimmel, Bader Alhaddad, Stefanie Beck‐Woedl, Merle Harrer, Daniela Karall, Lisa Kingelhoefer, Andreas Tzschach, Lars C. Matthies, Tim M. Strom, E. Bernd Ringelstein, Marc Sturm, Hartmut Engels, Markus Wolff, Holger Lerche, Tobias B. Haack

    Published 2019
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  13. 13
    Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy

    Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathy by Matias Wagner, Géza Berecki, Walid Fazeli, Claudia Nußbaum, Andreas W. Flemmer, Silvana Frizzo, F. Heer, Florian Heinen, Robert Horton, Henry Jacotin, WILLIAM G. MOTEL, Brian D. Spar, Christoph Klein, Corinna Siegel, Christoph Hübener, Sophia Stöcklein, Marco Paolini, Martin Staudt, Moritz Tacke, Markus Wolff, Steven Petrou, Marcio Souza, Ingo Borggraefe

    Published 2025
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  14. 14
    Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany

    Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany by Adam Strzelczyk, Malin Kalski, Thomas Bast, Adelheid Wiemer‐Kruel, U Bettendorf, Lara Kay, Matthias Kieslich, Gerhard Kluger, Gerhard Kurlemann, Patrick May, Bernd A. Neubauer, Tilman Polster, Arne Herting, Sarah von Spiczak, Regina Trollmann, Markus Wolff, John Irwin, Joe Carroll, Daniel Macdonald, Clive Pritchard, Karl Martin Klein, Felix Rosenow, Susanne Schubert‐Bast

    Published 2019
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  15. 15
    Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany

    Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany by Margarita Maltseva, Susanne Schubert‐Bast, Johann Philipp Zöllner, Thomas Bast, Patrick May, Sarah von Spiczak, Susanne Ruf, Regina Trollmann, Markus Wolff, Frauke Hornemann, Kerstin Alexandra Klotz, Julia Jacobs, Gerhard Kurlemann, Bernd A. Neubauer, Tilman Polster, Steffen Syrbe, Astrid Bertsche, U Bettendorf, Gerhard Kluger, Silke Flege, Felix Rosenow, Lara Kay, Adam Strzelczyk

    Published 2023
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  16. 16
    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

    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 by Adam Strzelczyk, Susanne Schubert‐Bast, Thomas Bast, U Bettendorf, Barbara Fiedler, Hajo M. Hamer, Arne Herting, Malin Kalski, Lara Kay, Matthias Kieslich, Karl Martin Klein, Gerhard Kluger, Gerhard Kurlemann, Patrick May, Bernd A. Neubauer, Tilman Polster, Sarah von Spiczak, Ulrich Stephani, Regina Trollmann, Adelheid Wiemer‐Kruel, Markus Wolff, John Irwin, Joe Carroll, Clive Pritchard, Felix Rosenow

    Published 2019
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  17. 17
    The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathy

    The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathy by Elena Gardella, Carla Marini, Marina Trivisano, Mark P. Fitzgerald, Michael Alber, Katherine B. Howell, Francesca Darra, Sabrina Siliquini, Bigna K. Bölsterli, Silva Masnada, Anna Pichiecchio, Katrine M. Johannesen, Birgit Jepsen, Elena Fontana, Gaia Anibaldi, Silvia Russo, Francesca Cogliati, Martino Montomoli, Nicola Specchio, Guido Rubboli, Pierangelo Veggiotti, Sándor Beniczky, Markus Wolff, Ingo Helbig, Federico Vigevano, Ingrid E. Scheffer, Renzo Guerrini, Rikke S. Møller

    Published 2018
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  18. 18
    Targeted next generation sequencing as a diagnostic tool in epileptic disorders

    Targeted next generation sequencing as a diagnostic tool in epileptic disorders by Johannes R. Lemke, Erik Riesch, Tim Scheurenbrand, Max Schubach, Christian Wilhelm, Isabelle Steiner, Jörg Hansen, Carolina Courage, Sabina Gallati, Sarah Bürki, Susi Strozzi, Barbara Goeggel Simonetti, Sebastian Grunt, Maja Steinlin, Michael Alber, Markus Wolff, Thomas Klopstock, Eva Christina Prott, Rüdiger Lorenz, Christiane Spaich, Sabine Rona, Maya Lakshminarasimhan, Judith F. Kroll, Thomas Dorn, Günter Krämer, Matthis Synofzik, Felicitas Becker, Yvonne G. Weber, Holger Lerche, Detlef Böhm, Saskia Biskup

    Published 2012
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  19. 19
    De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy

    De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy by Steffen Syrbe, Ulrike B. S. Hedrich, Erik Riesch, Tania Djémié, Stephan A. Müller, Rikke S. Møller, Bridget H. Maher, Laura Hernandez‐Hernandez, Matthis Synofzik, Hande Çağlayan, Mutluay Arslan, José M. Serratosa, Michael Nothnagel, Patrick May, Roland Krause, H. Löffler, Katja Detert, Thomas Dorn, Heinrich Vogt, Günter Krämer, Lüdger Schöls, Primus E. Mullis, Tarja Linnankivi, Anna-Elina Lehesjoki, Katalin Štěrbová, Dana Craiu, Dorota Hoffman‐Zacharska, Christian Korff, Yvonne G. Weber, Maja Steinlin, Sabina Gallati, Astrid Bertsche, Matthias K. Bernhard, Andreas Merkenschlager, Wieland Kieß, Michael Gonzalez, Stephan Züchner, Aarno Palotie, Arvid Suls, Peter De Jonghe, Ingo Helbig, Saskia Biskup, Markus Wolff, Snezana Maljevic, Rebecca Schüle, Sanjay M. Sisodiya, Sarah Weckhuysen, Holger Lerche, Johannes R. Lemke

    Published 2015
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  20. 20
    Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies

    Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies by Silvia Masnada, Ulrike B. S. Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Eric W. Klee, Brendan C. Lanpher, Ralitza H. Gavrilova, Matthis Synofzik, Thomas Bast, Kathleen M. Gorman, Mary D. King, Nicholas M. Allen, Judith Conroy, Bruria Ben Zeev, Michal Tzadok, Christian Korff, Fanny Dubois, Keri Ramsey, Vinodh Narayanan, José M. Serratosa, Beatriz G. Giráldez, Ingo Helbig, Eric D. Marsh, Margaret O’Brien, Christina A Bergqvist, Adrian Binelli, Brenda E. Porter, Eduardo José Bernardo Zaeyen, Dafne Dain Gandelman Horovitz, Markus Wolff, Dragan Marjanović, Hande Çağlayan, Mutluay Arslan, Sérgio D.J. Pena, Sanjay M. Sisodiya, Simona Balestrini, Steffen Syrbe, Pierangelo Veggiotti, Johannes R. Lemke, Rikke S. Møller, Holger Lerche, Guido Rubboli

    Published 2017
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