Resultats de la cerca - Fritz Zimprich

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  1. 1
    The clinical impact of pharmacogenetics on the treatment of epilepsy

    The clinical impact of pharmacogenetics on the treatment of epilepsy per Wolfgang Löscher, Ulrich Klotz, Fritz Zimprich, Dieter Schmidt

    Publicat 2008
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  2. 2
    Clinical Seizure Lateralization in Frontal Lobe Epilepsy

    Clinical Seizure Lateralization in Frontal Lobe Epilepsy per Silvia Bonelli, Stefanie Lurger, Fritz Zimprich, Elisabeth Stögmann, Eva Assem‐Hilger, Christoph Baumgartner

    Publicat 2007
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  3. 3
    Ancient and Recent Positive Selection Transformed Opioid cis-Regulation in Humans

    Ancient and Recent Positive Selection Transformed Opioid cis-Regulation in Humans per Matthew V. Rockman, Matthew W. Hahn, Nicole Soranzo, Fritz Zimprich, David B. Goldstein, Gregory A. Wray

    Publicat 2005
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  4. 4
    Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cells.

    Nucleocapsid or spike protein-specific CD4+ T lymphocytes protect against coronavirus-induced encephalomyelitis in the absence of CD8+ T cells. per Heinrich Körner, Andreas Schliephake, J. Winter, Fritz Zimprich, Hans Lassmann, Jonathon D. Sedgwick, Stuart G. Siddell, H. Wege

    Publicat 1991
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  5. 5
    Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society

    Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement to the Guidelines of the German Neurological Society per Nico Melzer, Tobias Ruck, Peter Fuhr, Ralf Gold, Reinhard Hohlfeld, Alexander Marx, Arthur Melms, Björn Tackenberg, Berthold Schalke, Christiane Schneider‐Gold, Fritz Zimprich, Sven G. Meuth, Heinz Wiendl

    Publicat 2016
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  6. 6
    Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome

    Increased serum neurofilament light chain concentration indicates poor outcome in Guillain-Barré syndrome per Patrick Altmann, Désirée De Simoni, Alexandra Kaider, Birgit Ludwig, Jakob Rath, Fritz Leutmezer, Fritz Zimprich, Romana Hoeftberger, Michael P. Lunn, Amanda Heslegrave, Thomas Berger, Henrik Zetterberg, Paulus Rommer

    Publicat 2020
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  7. 7
    RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

    RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy per Dennis Lal, Eva M. Reinthaler, Janine Altmüller, Mohammad R. Toliat, Holger Thiele, Peter Nürnberg, Holger Lerche, Andreas Hahn, Rikke S. Møller, Hiltrud Muhle, Thomas Sander, Fritz Zimprich, Bernd A. Neubauer

    Publicat 2013
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  8. 8
    Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum

    Mutations outside the N-terminal part of RBCK1 may cause polyglucosan body myopathy with immunological dysfunction: expanding the genotype–phenotype spectrum per Martin Krenn, Elisabeth Salzer, Ingrid Simonitsch‐Klupp, Jakob Rath, Matias Wagner, Tobias B. Haack, Tim M. Strom, Anne Schänzer, Manfred W. Kilimann, Ralf Schmidt, Klaus G. Schmetterer, Alexander Zimprich, Kaan Boztuğ, Andreas Hahn, Fritz Zimprich

    Publicat 2017
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  9. 9
    Pharmacoresistance in Epilepsy: A Pilot PET Study with the P‐Glycoprotein Substrate <i>R</i>‐[<sup>11</sup>C]verapamil

    Pharmacoresistance in Epilepsy: A Pilot PET Study with the P‐Glycoprotein Substrate <i>R</i>‐[<sup>11</sup>C]verapamil per Oliver Langer, Martin Bauer, Alexander Hammers, Rudolf Karch, Ekaterina Pataraia, Matthias J. Koepp, Aiman Abrahim, Gert Luurtsema, Martin Brunner, Raute Sunder‐Plaßmann, Fritz Zimprich, Christian Joukhadar, Stephan Gentzsch, Robert Dudczak, Kurt Kletter, Markus Müller, Christoph Baumgartner

    Publicat 2007
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  10. 10
    Analysis of <i>ELP4</i>,<i> SRPX2</i>, and interacting genes in typical and atypical rolandic epilepsy

    Analysis of <i>ELP4</i>,<i> SRPX2</i>, and interacting genes in typical and atypical rolandic epilepsy per Eva M. Reinthaler, Dennis Lal, Wiktor Jurkowski, Martha Feucht, Hannelore Steinböck, U Gruber‐Sedlmayr, Gabriel M. Ronen, Julia Geldner, Edda Haberlandt, Birgit Neophytou, Andreas Hahn, Janine Altmüller, Holger Thiele, Mohammad R. Toliat, Holger Lerche, Peter Nürnberg, Thomas Sander, Bernd A. Neubauer, Fritz Zimprich

    Publicat 2014
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  11. 11
    Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2

    Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2 per Elisabeth Stögmann, Eva M. Reinthaler, Salwa El Tawil, Mohammed A. El Etribi, Mahmoud Hemeda, Nevine El Nahas, Ahmed Mashhour Gaber, Amal Fouad, Sherif Edris, Anna Benet‐Pagès, Sebastian Eck, Ekaterina Pataraia, Davide Mei, Alexis Brice, Suzanne Lesage, Renzo Guerrini, Fritz Zimprich, Tim M. Strom, Alexander Zimprich

    Publicat 2013
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  12. 12
    B Cell Depletion and <scp>SARS‐CoV</scp>‐2 Vaccine Responses in Neuroimmunologic Patients

    B Cell Depletion and <scp>SARS‐CoV</scp>‐2 Vaccine Responses in Neuroimmunologic Patients per Barbara Kornek, Fritz Leutmezer, Paulus Rommer, Maximilian Koblischke, Lisa Schneider, Helmuth Haslacher, Renate Thalhammer, Fritz Zimprich, Gudrun Zulehner, Gabriel Bsteh, Assunta Dal‐Bianco, Walter Rinner, Karin Zebenholzer, Isabella Wimmer, Anja Steinmaurer, Marianne Graninger, Margareta Mayer, Kilian Roedl, Thomas Berger, Stefan Winkler, Judith H. Aberle, Selma Tobudic

    Publicat 2022
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  13. 13
    Rare exonic deletions of the <scp><i>RBFOX1</i></scp> gene increase risk of idiopathic generalized epilepsy

    Rare exonic deletions of the <scp><i>RBFOX1</i></scp> gene increase risk of idiopathic generalized epilepsy per Dennis Lal, Holger Trucks, Rikke S. Møller, Helle Hjalgrim, Bobby P.C. Koeleman, Carolien G. F. de Kovel, Frank Visscher, Yvonne G. Weber, Holger Lerche, Felicitas Becker, Christoph J. Schankin, Bernd A. Neubauer, Rainer Surges, Wolfram S. Kunz, Fritz Zimprich, André Franke, Thomas Illig, Janina S. Ried, Costin Leu, Peter Nürnberg, Thomas Sander

    Publicat 2013
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  14. 14
    Guideline for the management of myasthenic syndromes

    Guideline for the management of myasthenic syndromes per Heinz Wiendl, Angela Abicht, Andrew Chan, Adela Della Marina, Tim Hagenacker, Khosro Hekmat, Sarah Hoffmann, Hans-Stefan Hoffmann, Sebastian Jander, Christian W. Keller, Alexander Marx, Arthur Melms, Nico Melzer, Wolfgang Müller‐Felber, Marc Pawlitzki, Jens‐Carsten Rückert, Ulrike Schara‐Schmidt, Christiane Schneider‐Gold, Benedikt Schoser, Bettina Schreiner, Michael Schroeter, B Schubert, Jörn-Peter Sieb, Fritz Zimprich, Andreas Meisel

    Publicat 2023
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  15. 15
    A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease

    A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease per Alexander Zimprich, Anna Benet‐Pagès, Walter Struhal, Elisabeth Graf, Sebastian Eck, Marc N. Offman, Dietrich Haubenberger, Sabine Spielberger, Eva C. Schulte, Peter Lichtner, Shaila C. Rössle, Norman Klopp, Elisabeth Wolf, Klaus Seppi, Walter Pirker, Stefan Presslauer, Brit Mollenhauer, Regina Katzenschlager, Thomas Foki, Christoph Hotzy, Eva M. Reinthaler, Ashot S. Harutyunyan, Róbert Královics, Annette Peters, Fritz Zimprich, Thomas Brücke, Werner Poewe, Eduard Auff, Claudia Trenkwalder, Burkhard Rost, Gerhard Ransmayr, Juliane Winkelmann, Thomas Meitinger, Tim M. Strom

    Publicat 2011
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  16. 16
    Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathy

    Antibodies to the Caspr1/contactin-1 complex in chronic inflammatory demyelinating polyradiculoneuropathy per Elba Pascual‐Goñi, Janev Fehmi, Cinta Lleixà, L. Aguilar, Jérôme Devaux, Romana Höftberger, Émilien Delmont, Kathrin Doppler, Claudia Sommer, Aleksandar Radunović, Alejandra Carvajal, Shane Smyth, Laura Williams, Radim Mazanec, Veronika Potočková, N. Hinds, Julien Cassereau, Karine Viala, Mathilde Lefilliatre, Guillaume Nicolas, Peter Foley, Frank Leypoldt, Stephen Keddie, Michael P. Lunn, Fritz Zimprich, Vharoon Sharma Nunkoo, Wolfgang N. Löscher, Laura Martínez‐Martínez, Jordi Díaz‐Manera, Ricard Rojas‐García, Isabel Illa, Simon Rinaldi, Luís Querol

    Publicat 2021
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  17. 17
    16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

    16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy per 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

    Publicat 2014
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  18. 18
    Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

    Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity per Tõnu Esko, Massimo Mezzavilla, Mari Nelis, Christelle Borel, Tadeusz Dębniak, Eveliina Jakkula, Antonio Julià, Sena Karachanak-Yankova, Andrey Khrunin, Péter Kisfali, Veronika Krulišová, Zita Aušrelė Kučinskienė, Karola Rehnström, Michela Traglia, Liene Ņikitina-Zaķe, Fritz Zimprich, Stylianos E. Antonarakis, Xavier Estivill, Damjan Glavač, Marta Gut, Jānis Kloviņš, Michael Krawczak, Vaidutis Kučinskas, Mark Lathrop, Milan Maçek, Sara Marsal, Thomas Meitinger, Béla Melegh, Limborskaia Sa, Jan Lubiński, Aarno Paolotie, Stefan Schreiber, Драга Тончева, Daniela Toniolo, H‐Erich Wichmann, Alexander Zimprich, Mait Metspalu, Paolo Gasparini, Andres Metspalu, Pio D’Adamo

    Publicat 2012
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  19. 19
    Genetic Structure of Europeans: A View from the North–East

    Genetic Structure of Europeans: A View from the North–East per Mari Nelis, Tõnu Esko, Reedik Mägi, Fritz Zimprich, Alexander Zimprich, Драга Тончева, Sena Karachanak-Yankova, T. Piskáčková, Ivan Balaščák, Leena Peltonen, Eveliina Jakkula, Karola Rehnström, Mark Lathrop, Simon Heath, Pilar Galán, Stefan Schreiber, Thomas Meitinger, Arne Pfeufer, H‐Erich Wichmann, Béla Melegh, Noémi Polgár, Daniela Toniolo, Paolo Gasparini, Pio D’Adamo, Jānis Kloviņš, Liene Ņikitina-Zaķe, Vaidutis Kučinskas, Jūratė Kasnauskienė, Jan Lubiński, Tadeusz Dębniak, Limborskaia Sa, Andrey Khrunin, Xavier Estivill, Raquel Rabionet, Sara Marsal, Antonio Julià, Stylianos E. Antonarakis, Samuel Deutsch, Christelle Borel, Homa Attar, Maryline Gagnebin, Milan Maçek, Michael Krawczak, Maido Remm, Andres Metspalu

    Publicat 2009
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  20. 20
    Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies

    Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies per Dennis Lal, Ann‐Kathrin Ruppert, Holger Trucks, Herbert Schulz, Carolien G. F. de Kovel, Dorothee Kasteleijn‐Nolst Trenité, Anja C. M. Sonsma, Bobby P.C. Koeleman, Dick Lindhout, Yvonne G. Weber, Holger Lerche, Claudia Kapser, Christoph J. Schankin, Wolfram S. Kunz, Rainer Surges, Christian E. Elger, Verena Gaus, Bettina Schmitz, Katherine L. Helbig, Hiltrud Muhle, Ulrich Stephani, Karl Martin Klein, Felix Rosenow, Bernd A. Neubauer, Eva M. Reinthaler, Fritz Zimprich, Martha Feucht, Rikke S. Møller, Helle Hjalgrim, Peter De Jonghe, Arvid Suls, Wolfgang Lieb, André Franke, Konstantin Strauch, Christian Gieger, Claudia Schurmann, Ulf Schminke, Peter Nürnberg, Thomas Sander

    Publicat 2015
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