Результаты поиска - Rudolf Korinthenberg

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  1. 1
    Natural history and treatment effects in Guillain-Barre syndrome: a multicentre study.

    Natural history and treatment effects in Guillain-Barre syndrome: a multicentre study. по Rudolf Korinthenberg, Jürgen Schulte Mönting

    Опубликовано 1996
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    Artigo
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  2. 2
    Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta‐analysis

    Efficacy and safety of corticosteroids and ACTH in epileptic syndromes beyond Infantile Epileptic Spasms Syndrome (IESS): A systematic review and meta‐analysis по Rudolf Korinthenberg, Thomas Bast, Edda Haberlandt, Ulrich Stephani, Adam Strzelczyk, Gerta Rücker

    Опубликовано 2024
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    Revisão
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  3. 3
    High frequency oscillations mirror disease activity in patients with focal cortical dysplasia

    High frequency oscillations mirror disease activity in patients with focal cortical dysplasia по Karolin Kerber, Pierre LeVan, Matthias Dümpelmann, Susanne Fauser, Rudolf Korinthenberg, Andreas Schulze‐Bonhage, Julia Jacobs

    Опубликовано 2013
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    Artigo
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  4. 4
    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 по Georgia Ramantani, Bigna K. Bölsterli, Michael Alber, Joerg Klepper, Rudolf Korinthenberg, Gerhard Kurlemann, Daniel Tibussek, Markus Wolff, Bernhard Schmitt

    Опубликовано 2022
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    Artigo
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  5. 5
    Posterior cortex epilepsy surgery in childhood and adolescence: Predictors of long-term seizure outcome

    Posterior cortex epilepsy surgery in childhood and adolescence: Predictors of long-term seizure outcome по Georgia Ramantani, Angeliki Stathi, Armin Brandt, Karl Strobl, Susanne Schubert‐Bast, Gert Wiegand, Rudolf Korinthenberg, Vera Van Velthoven, Josef Zentner, Andreas Schulze‐Bonhage, Thomas Bast

    Опубликовано 2017
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    Artigo
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  6. 6
    Clinical characteristics in focal cortical dysplasia: a retrospective evaluation in a series of 120 patients

    Clinical characteristics in focal cortical dysplasia: a retrospective evaluation in a series of 120 patients по Susanne Fauser, Hans‐Jürgen Huppertz, Thomas Bast, Karl Strobl, Georgios Pantazis, Dirk-Matthias Altenmueller, Bertram Feil, Sabine Rona, Christoph Kurth, D. Rating, Rudolf Korinthenberg, Bernhard J. Steinhoff, Benedikt Volk, Andreas Schulze‐Bonhage

    Опубликовано 2006
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    Artigo
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  7. 7
    Epilepsy Surgery in the First 3 Years of Life: Predictors of Seizure Freedom and Cognitive Development

    Epilepsy Surgery in the First 3 Years of Life: Predictors of Seizure Freedom and Cognitive Development по Navah Ester Kadish, Thomas Bast, Gitta Reuner, Kathrin Wagner, H. Mayer, Susanne Schubert‐Bast, Gert Wiegand, Karl Strobl, Armin Brandt, Rudolf Korinthenberg, Vera Van Velthoven, Andreas Schulze‐Bonhage, Josef Zentner, Georgia Ramantani

    Опубликовано 2018
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    Artigo
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  8. 8
    Seizure control and developmental trajectories after hemispherotomy for refractory epilepsy in childhood and adolescence

    Seizure control and developmental trajectories after hemispherotomy for refractory epilepsy in childhood and adolescence по Georgia Ramantani, Navah Ester Kadish, Armin Brandt, Karl Strobl, Angeliki Stathi, Gert Wiegand, Susanne Schubert‐Bast, H. Mayer, Kathrin Wagner, Rudolf Korinthenberg, Ulrich Stephani, Vera Van Velthoven, Josef Zentner, Andreas Schulze‐Bonhage, Thomas Bast

    Опубликовано 2013
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    Artigo
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  9. 9
    Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations

    Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations по Martin Zenker, Katarina Lehmann, AL Schulz, Heidi Barth, D. Hansmann, Rainer Koenig, Rudolf Korinthenberg, Martina Kreiß‐Nachtsheim, Peter Meinecke, Susanne Morlot, Stefan Mundlos, Anne S. Quante, Salmo Raskin, Dirk Schnabel, Lore Wehner, Christian P. Kratz, Denise Horn, Kerstin Kutsche

    Опубликовано 2006
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    Artigo
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  10. 10
    ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies

    ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies по Sebahattin Çirak, A. Reghan Foley, Ralf Herrmann, Tobias Willer, Shu Yau, Elizabeth Stevens, Silvia Torelli, Lina Brodd, Alisa Kamynina, Petr Vondráček, Helen Roper, Cheryl Longman, Rudolf Korinthenberg, Gianni Marrosu, Peter Nürnberg, Daniel E. Michele, Vincent Plagnol, Matt Hurles, Steven A. Moore, Caroline A. Sewry, Kevin P. Campbell, Thomas Voït, Francesco Muntoni

    Опубликовано 2013
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    Artigo
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  11. 11
    Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4

    Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4 по Claudia Stendel, Andreas Roos, Tine Deconinck, Jorge A. Pereira, François Castagner, Axel Niemann, Janbernd Kirschner, Rudolf Korinthenberg, Uwe‐Peter Ketelsen, Esra Battaloğlu, Yeşim Parman, Garth A. Nicholson, Robert Ouvrier, Jürgen Seeger, Peter De Jonghe, Joachim Weis, Alexander Krüttgen, Sabine Rudnik–Schöneborn, Carsten Bergmann, Ueli Suter, Klaus Zerres, Vincent Timmerman, João B. Relvas, Jan Senderek

    Опубликовано 2007
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    Artigo
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  12. 12
    Pontocerebellar hypoplasia type 1

    Pontocerebellar hypoplasia type 1 по Sabine Rudnik–Schöneborn, Jan Senderek, Joanna C. Jen, Gunnar Houge, Pavel Seeman, Alena Puchmajerová, Luitgard Graul‐Neumann, Ulrich Seidel, Rudolf Korinthenberg, Janbernd Kirschner, Jürgen Seeger, Monique M. Ryan, Francesco Muntoni, Maja Steinlin, László Sztriha, J. Colomer, Christoph Hübner, Knut Brockmann, Lionel Van Maldergem, Manuel Schiff, Andreas Holzinger, P. G. Barth, William Reardon, Michael Yourshaw, Stanley F. Nelson, Thomas Eggermann, Klaus Zerres

    Опубликовано 2013
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    Artigo
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  13. 13
    Oligoclonal bands predict multiple sclerosis in children with optic neuritis

    Oligoclonal bands predict multiple sclerosis in children with optic neuritis по Nicole Heußinger, Evangelos Kontopantelis, Janina Gburek‐Augustat, Andreas Jenke, G. Vollrath, Rudolf Korinthenberg, Peter Hofstetter, Sascha Meyer, Isabel Brecht, Barbara Kornek, Peter Herkenrath, Mareike Schimmel, K. Wenner, Martin Häusler, S. Lutz, Michael Karenfort, Astrid Blaschek, Martin Smitka, Stephanie Karch, Martin Piepkorn, Kevin Rostásy, Thomas Lücke, Christian Weber, Regina Trollmann, Jörg Klepper, Martin Häussler, Regina Hofmann, Robert Weissert, Andreas Merkenschlager, Mathias Buttmann

    Опубликовано 2015
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    Artigo
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  14. 14
    Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia

    Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia по Yasmin Namavar, P. G. Barth, Paul R. Kasher, Fred van Ruissen, Knut Brockmann, G. Bernert, Karin Writzl, Karen Ventura, Kwang‐Ting Cheng, Donna M. Ferriero, Lina Basel‐Vanagaite, Veerle Rc Eggens, Ingeborg Krägeloh‐Mann, Linda De Meırleır, Mary D. King, John M. Graham, Arpad von Moers, N. A. V. M. Knoers, László Sztriha, Rudolf Korinthenberg, PCH Consortium, William B. Dobyns, Frank Baas, Bwee Tien Poll‐The

    Опубликовано 2010
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    Artigo
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