Search Results - Thomas Sander

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  1. 1
    Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy

    Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy by Bin Tang, Thomas Sander, Kimberley B. Craven, Anne Hempelmann, Andrew Escayg

    Published 2007
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  2. 2
    Circulating microRNAs as Biomarkers for Detection of Autologous Blood Transfusion

    Circulating microRNAs as Biomarkers for Detection of Autologous Blood Transfusion by Nicolas Leuenberger, Yorck Olaf Schumacher, Sylvain Pradervand, Thomas Sander, Martial Saugy, Torben Pottgießer

    Published 2013
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  3. 3
    KIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory

    KIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory by Claudia Preuschhof, Hauke R. Heekeren, Shu Li, Thomas Sander, Ulman Lindenberger, Lars Bäckman

    Published 2009
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  4. 4
    A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy

    A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy by Andrew Escayg, Armin Heils, Bryan T. MacDonald, Karsten Haug, Thomas Sander, Miriam H. Meisler

    Published 2001
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  5. 5
    Association of attentional network function with exon 5 variations of the CHRNA4 gene

    Association of attentional network function with exon 5 variations of the CHRNA4 gene by Georg Winterer, Francesco Musso, Andreas Konrad, Goran Vučurević, Peter Stoeter, Thomas Sander, Juergen Gallinat

    Published 2007
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  6. 6
    Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene<i>NPRL3</i>

    Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene<i>NPRL3</i> by Georg‐Christoph Korenke, Marlene Eggert, Hölger Thiele, Peter Nürnberg, Thomas Sander, Ortrud K. Steinlein

    Published 2016
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  7. 7
    TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue

    TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue by Katharina Pernhorst, Stefan Herms, Per Hoffmann, Sven Cichon, Herbert Schulz, Thomas Sander, Susanne Schoch, Albert J. Becker, Alexander Grote

    Published 2013
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  8. 8
    Variations in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) are Associated with Bipolar I Disorder

    Variations in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) are Associated with Bipolar I Disorder by Falk W. Lohoff, John P. Dahl, Thomas N. Ferraro, Steven E. Arnold, Jürgen Gallinat, Thomas Sander, Wade H. Berrettini

    Published 2006
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  9. 9
    Brief research communication: serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders

    Brief research communication: serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders by Margret R. Hoehe, Birgit Wendel, Ingrid Grunewald, Pierre Chiaroni, Nicolas Lévy, Deborah Morris‐Rosendahl, Jean-Paul Macher, Thomas Sander, Marc‐Antoine Crocq

    Published 1998
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  10. 10
    Ebbinghaus Revisited: Influences of the BDNF Val<i>66</i>Met Polymorphism on Backward Serial Recall Are Modulated by Human Aging

    Ebbinghaus Revisited: Influences of the BDNF Val<i>66</i>Met Polymorphism on Backward Serial Recall Are Modulated by Human Aging by Shu Li, Christian Chicherio, Lars Nyberg, Timo von Oertzen, Irene E. Nagel, Goran Papenberg, Thomas Sander, Hauke R. Heekeren, Ulman Lindenberger, Lars Bäckman

    Published 2009
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  11. 11
    Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing

    Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing by Dennis Lal, Bernd A. Neubauer, Mohammad R. Toliat, Janine Altmüller, Holger Thiele, Peter Nürnberg, Clemens Kamrath, Anne Schänzer, Thomas Sander, Andreas Hahn, Michael Nothnagel

    Published 2016
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  12. 12
    Coding and Noncoding Variation of the Human Calcium-Channel β4-Subunit Gene CACNB4 in Patients with Idiopathic Generalized Epilepsy and Episodic Ataxia

    Coding and Noncoding Variation of the Human Calcium-Channel β4-Subunit Gene CACNB4 in Patients with Idiopathic Generalized Epilepsy and Episodic Ataxia by Andrew Escayg, Michel De Waard, David D. Lee, Delphine Bichet, Peter Wolf, Thomas A. Mayer, Janine L. Johnston, Robert W. Baloh, Thomas Sander, Miriam H. Meisler

    Published 2000
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  13. 13
    RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy

    RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy by 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

    Published 2013
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  14. 14
    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 by 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

    Published 2014
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  15. 15
    Extending the phenotypic spectrum of <i><scp>RBFOX</scp>1</i> deletions: Sporadic focal epilepsy

    Extending the phenotypic spectrum of <i><scp>RBFOX</scp>1</i> deletions: Sporadic focal epilepsy by 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

    Published 2015
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  16. 16
    A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy

    A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy by Gianpiero L. Cavalleri, Sophie Nicole, Nicole Soranzo, John C. Mulley, Colin P. Doherty, Ashish Kapoor, Chantal Depondt, John Lynch, Ingrid E. Scheffer, Armin Heils, Anne Gehrmann, Peter Kinirons, Sonia Gandhi, Parthasarathy Satishchandra, Nicholas Wood, Anuranjan Anand, Thomas Sander, Samuel F. Berkovic, Norman Delanty, David B. Goldstein, Sanjay M. Sisodiya

    Published 2007
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  17. 17
    Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus

    Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus by Herbert Schulz, Ann‐Kathrin Ruppert, Stefan Herms, Christiane Wolf, Nazanin Mirza‐Schreiber, Oliver Stegle, Darina Czamara, Andreas J. Forstner, Sugirthan Sivalingam, Susanne Schoch, Susanne Moebus, Benno Pütz, Axel M. Hillmer, Nadine Fricker, Hartmut Vatter, Bertram Müller‐Myhsok, Markus M. Nöthen, Albert J. Becker, Per Hoffmann, Thomas Sander, Sven Cichon

    Published 2017
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  18. 18
    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 by 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

    Published 2013
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  19. 19
    Retraction Note: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

    Retraction Note: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies by Karsten Haug, Maike Warnstedt, Alexi K. Alekov, Thomas Sander, Alfredo Ramı́rez, Barbara Poser, Snezana Maljevic, Simon Hebeisen, Christian Kubisch, Johannes Rebstock, Steve Horvath, Kerstin Hallmann, Joern Dullinger, Birgit Rau, Fritz Haverkamp, Stefan Beyenburg, Herbert Schulz, Diéter Janz, B. Giese, Gerhard Müller‐Newen, Peter Propping, Christian E. Elger, Christoph Fahlke, Holger Lerche, Armin Heils

    Published 2009
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  20. 20
    Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies

    Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies by Karsten Haug, Maike Warnstedt, Alexi K. Alekov, Thomas Sander, Alfredo Ramı́rez, Barbara Poser, Snezana Maljevic, Simon Hebeisen, Christian Kubisch, Johannes Rebstock, Steve Horvath, Kerstin Hallmann, Joern Dullinger, Birgit Rau, Fritz Haverkamp, Stefan Beyenburg, Herbert Schulz, Diéter Janz, B. Giese, Gerhard Müller‐Newen, Peter Propping, Christian E. Elger, Christoph Fahlke, Holger Lerche, Armin Heils

    Published 2003
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