Search Results - Gregor Kuhlenbäumer

Refine Results
  1. 1
    Novel genomic techniques open new avenues in the analysis of monogenic disorders

    Novel genomic techniques open new avenues in the analysis of monogenic disorders by Gregor Kuhlenbäumer, Julia Hullmann, Silke Appenzeller

    Published 2010
    Get full text
    Revisão
    Save to List
    Saved in:
  2. 2
    Variation in the PDE4D Gene and Ischemic Stroke Risk

    Variation in the PDE4D Gene and Ischemic Stroke Risk by Steve Bevan, Martin Dichgans, Andreas Gschwendtner, Gregor Kuhlenbäumer, E.B. Ringelstein, Hugh S. Markus

    Published 2008
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  3. 3
    The Role of Aquaporin-4 Polymorphisms in the Development of Brain Edema After Middle Cerebral Artery Occlusion

    The Role of Aquaporin-4 Polymorphisms in the Development of Brain Edema After Middle Cerebral Artery Occlusion by Ilka Kleffner, May Bungeroth, Hagen Schiffbauer, W.-R. Schäbitz, E. Bernd Ringelstein, Gregor Kuhlenbäumer

    Published 2008
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  4. 4
    Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution

    Acute physical exercise improves shifting in adolescents at school: evidence for a dopaminergic contribution by Timo Berse, Kathrin Rolfes, Jonathan Barenberg, Stephan Dutke, Gregor Kuhlenbäumer, Klaus Völker, Bernward Winter, Michael Wittig, Stefan Knecht

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules

    Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules by Xiaobo Bai, Jonathan R. Bowen, Tara K. Knox, Kaifeng Zhou, Manuela Pendziwiat, Gregor Kuhlenbäumer, Charles V. Sindelar, Elias T. Spiliotis

    Published 2013
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  6. 6
    Febrile infection‐related epilepsy syndrome (FIRES) is not caused by <i>SCN1A, POLG, PCDH19</i> mutations or rare copy number variations

    Febrile infection‐related epilepsy syndrome (FIRES) is not caused by <i>SCN1A, POLG, PCDH19</i> mutations or rare copy number variations by Silke Appenzeller, Ingo Helbig, Ulrich Stephani, Martin Häusler, Gerhard Kluger, May Bungeroth, Stefanie H. Müller, Gregor Kuhlenbäumer, Andreas van Baalen

    Published 2012
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor

    Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor by Sandra Thier, Delia Lorenz, Michael Nothnagel, Caroline Poremba, Frank Papengut, Silke Appenzeller, Steffen Paschen, Frank Hofschulte, Anna-Christina Hussl, Sascha Hering, Werner Poewe, Friedrich Asmus, Thomas Gasser, Lüdger Schöls, Kaare Christensen, Almut Nebel, Stefan Schreiber, Stephan Klebe, Günther Deuschl, Gregor Kuhlenbäumer

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  8. 8
    Knowledge gaps and research recommendations for essential tremor

    Knowledge gaps and research recommendations for essential tremor by Franziska Hopfner, Dietrich Haubenberger, Wendy R. Galpern, Katrina Gwinn, Ashlee Van’t Veer, Samantha White, Kailash P. Bhatia, Charles H. Adler, David Eidelberg, William G. Ondo, Glenn T. Stebbins, Caroline M. Tanner, Rick C. Helmich, Fred A. Lenz, Roy V. Sillitoe, David E. Vaillancourt, Jerrold L. Vitek, Elan D. Louis, Holly A. Shill, Matthew P. Frosch, Tatiana Foroud, Gregor Kuhlenbäumer, Andrew Singleton, Claudia Testa, Mark Hallett, Rodger J. Elble, Günther Deuschl

    Published 2016
    Get full text
    Revisão
    Save to List
    Saved in:
  9. 9
    A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

    A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke by Daníel F. Guðbjartsson, Hilma Hólm, Sólveig Grétarsdóttir, Guðmar Þorleifsson, G. Bragi Walters, Guðmundur Þorgeirsson, Jeffrey R. Gulcher, Ellisiv B. Mathiesen, Inger Njølstad, Audhild Nyrnes, Tom Wilsgaard, Erin Mathiesen Hald, Kristian Hveem, Camilla Stoltenberg, Gayle Kucera, Tanya Stubblefield, Shannon Carter, Dan M. Roden, Maggie Ng, Larry Baum, Wing Yee So, Ka Sing Wong, Juliana C.N. Chan, Christian Gieger, H‐Erich Wichmann, Andreas Gschwendtner, Martin Dichgans, Gregor Kuhlenbäumer, Klaus Berger, E. Bernd Ringelstein, Steve Bevan, Hugh S. Markus, Konstantinos Kostulas, Jan Hillert, Sigurlaug Sveinbjörnsdóttir, Einar Már Valdimarsson, Maja‐Lisa Løchen, Ronald C.W., Dawood Darbar, Augustine Kong, Davíð O. Arnar, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Genome-wide association study in essential tremor identifies three new loci

    Genome-wide association study in essential tremor identifies three new loci by Stefanie H. Müller, Simon Girard, Franziska Hopfner, Nancy D. Merner, Cynthia V. Bourassa, Delia Lorenz, Lorraine N. Clark, Lukas Tittmann, Alexandra I. Soto‐Ortolaza, Stephan Klebe, Mark Hallett, Susanne A. Schneider, Colin A. Hodgkinson, Wolfgang Lieb, Zbigniew K. Wszołek, Manuela Pendziwiat, Oswaldo Lorenzo‐Betancor, Werner Poewe, Sara Ortega‐Cubero, Klaus Seppi, Alex Rajput, Anna Hussl, Ali H. Rajput, Daniela Berg, Patrick A. Dion, Isabel Wurster, Joshua Shulman, Karin Srulijes, Dietrich Haubenberger, Pau Pástor, Carles Vilariño‐Güell, Ronald B. Postuma, Geneviève Bernard, Karl‐Heinz Ladwig, Nicolas Dupré, Joseph Jankovic, Konstantin Strauch, Michel Panisset, Juliane Winkelmann, Claudia Testa, Eva Reischl, Kirsten E. Zeuner, Owen A. Ross, Thomas Arzberger, Sylvain Chouinard, Günther Deuschl, Elan D. Louis, Gregor Kuhlenbäumer, Guy A. Rouleau

    Published 2016
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    Association of Essential Tremor With Novel Risk Loci

    Association of Essential Tremor With Novel Risk Loci by Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, Veikko Vuokila, Miranda Medeiros, Gabrielle Houle, Fulya Akçimen, Jay P. Ross, Hélène Catoire, Mónica Díez-Fairén, Jooeun Kang, Stefanie H. Mueller, Simon Girard, Franziska Hopfner, Delia Lorenz, Lorraine N. Clark, Alexandra I. Soto‐Beasley, Stephan Klebe, Mark Hallett, Zbigniew K. Wszołek, Manuela Pendziwiat, Oswaldo Lorenzo‐Betancor, Klaus Seppi, Daniela Berg, Carles Vilariño‐Güell, Ronald B. Postuma, Geneviève Bernard, Nicolas Dupré, Joseph Jankovic, Claudia M. Testa, Owen A. Ross, Thomas Arzberger, Sylvain Chouinard, Elan D. Louis, Paola Mandich, Carmine Vitale, Paolo Barone, Elena García‐Martín, Hortensia Alonso‐Navarro, José A. G. Agúndez, Félix Javier Jiménez‐Jiménez, Pau Pástor, Alex Rajput, Günther Deuschl, Gregor Kuhlenbäumer, Inge A. Meijer, Patrick A. Dion, Guy A. Rouleau

    Published 2022
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  12. 12
    Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection

    Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection by Stéphanie Debette, Yoichiro Kamatani, Tiina M. Metso, Manja Kloß, Ganesh Chauhan, Stefan T. Engelter, Alessandro Pezzini, Vincent Thijs, Hugh S. Markus, Martin Dichgans, Christiane Wolf, Ralf Dittrich, Emmanuel Touzé, Andrew M. Southerland, Yves Samson, Shérine Abboud, Yannick Béjot, Valeria Caso, Anna Bersano, Andreas Gschwendtner, Maria Sessa, John Cole, Chantal Lamy, Elisabeth Medeiros, Simone Beretta, Leo H. Bonati, Armin Grau, Patrik Michel, Jennifer J. Majersik, Pankaj Sharma, Ludmila А. Kalashnikova, Maria Nazarova, Л А Добрынина, Eva Bartels, B. Guillon, Evita G. van den Herik, Israel Fernández‐Cadenas, Katarina Jood, Michael A. Nalls, Frank‐Erik de Leeuw, Christina Jern, Yu‐Ching Cheng, Inge Werner, Antti J. Metso, Christoph Lichy, Philippe Lyrer, Tobias Brandt, Giorgio B. Boncoraglio, Heinz‐Erich Wichmann, Christian Gieger, Andrew D. Johnson, Thomas Böttcher, Maurizio Castellano, Dominique Arveiler, M. Arfan Ikram, Monique M.B. Breteler, Alessandro Padovani, James F. Meschia, Gregor Kuhlenbäumer, Arndt Rolfs, Bradford B. Worrall, Ringelstein Erich-Bernd, Diana Zélénika, Turgut Tatlisumak, Mark Lathrop, Didier Leys, Philippe Amouyel, Jean Dallongeville, Olivier Godefroy, Sandrine Canaple

    Published 2014
    Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

    De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome by Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, Yvonne G. Weber, Sarah Weckhuysen, Dana Craiu, Aleksandra Siekierska, Tania Djémié, Tatiana Afrikanova, Padhraig Gormley, Sarah von Spiczak, Gerhard Kluger, Catrinel Iliescu, Tiina Talvik, Inga Talvik, Cihan Meral, Hande Çağlayan, Beatriz G. Giráldez, José M. Serratosa, Johannes R. Lemke, Dorota Hoffman‐Zacharska, Elżbieta Szczepanik, Nina Barišić, Vladimı́r Komárek, Helle Hjalgrim, Rikke S. Møller, Tarja Linnankivi, Petia Dimova, Pasquale Striano, Federico Zara, Carla Marini, Renzo Guerrini, Christel Depienne, Stéphanie Baulac, Gregor Kuhlenbäumer, Alexander D. Crawford, Anna‐Elina Lehesjoki, Peter de Witte, Aarno Palotie, Holger Lerche, Camila V. Esguerra, Peter De Jonghe, Ingo Helbig, Rik Hendrickx, Philip Holmgren, Ulrich Stephani, Hiltrud Muhle, Manuela Pendiziwiat, Silke Appenzeller, Kaja Kristine Selmer, Eva H. Brilstra, Bobby P.C. Koeleman, Felix Rosenow, Eric LeGuern, Katalin Štěrbová, Budisteanu Magdalena, Gherghiceanu Rodica, Oana Tarta Arsene, Barca Diana, Rosa Guerrero, Laura Ortega, Албена Тодорова, Andrey Kirov, Angela Robbiano, Mutluay Arslan, Uluç Yiş, Vanja Ivanović

    Published 2013
    Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Motor, cognitive and mobility deficits in 1000 geriatric patients: protocol of a quantitative observational study before and after routine clinical geriatric treatment – the ComOn-study

    Motor, cognitive and mobility deficits in 1000 geriatric patients: protocol of a quantitative observational study before and after routine clinical geriatric treatment – the ComOn-... by Johanna Geritz, Sara Maetzold, Maren Steffen, Andrea Pilotto, Marta Francisca Corrà, Mariana Moscovich, Maria Cristina Rizzetti, Barbara Borroni, Alessandro Padovani, Annekathrin Alpes, Corinna Bang, Igor Barcellos, Ralf Baron, Thorsten Bartsch, Jos S. Becktepe, Daniela Berg, Lu M. Bergeest, Philipp Bergmann, Raquel Bouça‐Machado, Michael Drey, Morad Elshehabi, Susan Farahmandi, Joaquim J. Ferreira, André Franke, Anja Friederich, Corinna Geisler, Philipp Hüllemann, Janne Gierthmühlen, Oliver Granert, Sebastian Heinzel, Maren K. Heller, Markus A. Hobert, M. Hofmann, Björn Jemlich, Laura Kerkmann, Stephanie C. Knüpfer, Katharina Krause, Maximilian Kress, Sonja Krupp, Jennifer Kudelka, Gregor Kuhlenbäumer, Roland Kurth, Frank Leypoldt, Corina Maetzler, Luı́s F. Maia, Andreas Moewius, Patricia Neumann, Katharina Niemann, Christian Ortlieb, Steffen Paschen, Minh H. Pham, Thomas Puehler, Franziska Radloff, Christian Riedel, Marten Rogalski, Simone Sablowsky, Elena M. Schanz, Linda Schebesta, Andreas Schicketmüller, Simone Studt, Martina Thieves, Lars Tönges, Sebastian Ullrich, Péter Urbán, Nuno Vila‐Chã, Anna Wiegard, Elke Warmerdam, Tobias Warnecke, Michael Weiß, Julius Welzel, Clint Hansen, Walter Maetzler

    Published 2020
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Genome-wide association study of autopsy-confirmed Multiple System Atrophy identifies common variants near <i>ZIC1</i> and <i>ZIC4</i>

    Genome-wide association study of autopsy-confirmed Multiple System Atrophy identifies common variants near <i>ZIC1</i> and <i>ZIC4</i> by Franziska Hopfner, Anja Tietz, Viktoria Ruf, Owen A. Ross, Shunsuke Koga, Dennis W. Dickson, Adriano Aguzzi, Johannes Attems, Thomas G. Beach, Allison Beller, Vivianna M. Van Deerlin, Paula Desplats, Günther Deuschl, Charles Duyckaerts, David Ellinghaus, Valentin Evsyukov, Margaret E. Flanagan, André Franke, Matthew P. Frosch, Marla Gearing, Ellen Gelpí, Bernardino Ghetti, Jonathan D. Glass, Lea T. Grinberg, Glenda M. Halliday, Ingo Helbig, Matthias Höllerhage, Inge Huitinga, David J. Irwin, Dirk Keene, Gábor G. Kovács, Edward B. Lee, Johannes Levin, Marı́a José Martı́, Ian R. Mackenzie, Ian G. McKeith, Catriona McLean, Brit Mollenhauer, Manuela Neumann, Kathy L. Newell, Alexander Pantelyat, Manuela Pendziwiat, Annette Peters, Laura Molina‐Porcel, Alberto Rábano, Radoslav Matěj, Alex Rajput, Ali H. Rajput, Regina Reimann, William K. Scott, William W. Seeley, Sashika Selvackadunco, Tanya Simuni, Christine Stadelmann, Per Svenningsson, Alan Thomas, Claudia Trenkwalder, Claire Troakes, John Q. Trojanowski, Charles L. White, Tao Xie, Teresa Ximelis, Justo Yebenes, Ulrich Müller, Daniela Berg, Jochen Herms, Gregor Kuhlenbäumer, Günter U. Höglinger

    Published 2021
    Get full text Get full text
    Pré-impressão
    Save to List
    Saved in:
  16. 16
    Diagnosis and treatment of Parkinson´s disease (guideline of the German Society for Neurology)

    Diagnosis and treatment of Parkinson´s disease (guideline of the German Society for Neurology) by Günter U. Höglinger, Mathias Bähr, Jos S. Becktepe, Daniela Berg, Kathrin Brockmann, Carsten Buhmann, Andrés Ceballos-Baumann, Joseph Claßen, Cornelius Deuschl, Günther Deuschl, Richard Dodel, Georg Ebersbach, Carsten Eggers, Thilo van Eimeren, Alessandra Fanciulli, Bruno Fimm, Ann‐Kristin Folkerts, Madeleine Gausepohl, Alkomiet Hasan, Wiebke Hermann, Rüdiger Hilker-Roggendorf, Günter U. Höglinger, Matthias Höllerhage, Franziska Hopfner, Wolfgang H. Jost, Elke Kalbe, Jan Kassubek, Stephan Klebe, Christine Klein, Martin Klietz, Thomas Koeglsperger, Andrea A. Kühn, Paul Krack, Florian Krismer, Gregor Kuhlenbäumer, Johannes Levin, Inga Liepelt‐Scarfone, Paul Lingor, Kai F. Loewenbrück, Matthias Löhle, Stefan Lorenzl, Sylvia Maaß, Walter Maetzler, Regina Menzel, Philipp T. Meyer, Brit Mollenhauer, Manuela Neumann, Per Odin, Tiago F. Outeiro, Monika Pötter‐Nerger, René Reese, Kathrin Reetz, Olaf Rieß, Viktoria Ruf, Anja Schneider, Christoph Schrader, Alfons Schnitzler, Klaus Seppi, Friederike Sixel‐Döring, Alexander Storch, Lars Tönges, Claudia Trenkwalder, Uwe Walter, Tobias Wächter, Tobias Warnecke, Florian Wegner, Christian Winkler, Karsten Witt, Dirk Woitalla, Kirsten E. Zeuner, Claudia Trenkwalder

    Published 2024
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  17. 17
    Common Variants Near <scp>ZIC1</scp> and <scp>ZIC4</scp> in Autopsy‐Confirmed Multiple System Atrophy

    Common Variants Near <scp>ZIC1</scp> and <scp>ZIC4</scp> in Autopsy‐Confirmed Multiple System Atrophy by Franziska Hopfner, Anja Tietz, Viktoria Ruf, Owen A. Ross, Shunsuke Koga, Dennis W. Dickson, Adriano Aguzzi, Johannes Attems, Thomas Beach, Allison Beller, William P. Cheshire, Vivianna M. Van Deerlin, Paula Desplats, Günther Deuschl, Charles Duyckaerts, David Ellinghaus, Valentin Evsyukov, Margaret E. Flanagan, André Franke, Matthew P. Frosch, Marla Gearing, Ellen Gelpí, Jay A. van Gerpen, Bernardino Ghetti, Jonathan D. Glass, Lea T. Grinberg, Glenda M. Halliday, Ingo Helbig, Matthias Höllerhage, Inge Huitinga, David J. Irwin, Dirk Keene, Gábor G. Kovács, Edward B. Lee, Johannes Levin, Marı́a José Martı́, Ian R. Mackenzie, Ian G. McKeith, Catriona McLean, Brit Mollenhauer, Manuela Neumann, Kathy L. Newell, Alexander Pantelyat, Manuela Pendziwiat, Annette Peters, Laura Molina‐Porcel, Alberto Rábano, Radoslav Matěj, Alex Rajput, Ali H. Rajput, Regina Reimann, William K. Scott, William W. Seeley, Sashika Selvackadunco, Tanya Simuni, Christine Stadelmann, Per Svenningsson, Alan Thomas, Claudia Trenkwalder, Claire Troakes, John Q. Trojanowski, Ryan J. Uitti, Charles L. White, Zbigniew K. Wszołek, Tao Xie, Teresa Ximelis, Justo Yebenes, Ulrich Müller, Daniela Berg, Jochen Herms, Gregor Kuhlenbäumer, Günter U. Höglinger

    Published 2022
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    Diagnostics and treatment of impulse control disorders, psychosis and delirium: systemic review-based recommendations - guideline “Parkinson’s disease” of the German Society of Neurology

    Diagnostics and treatment of impulse control disorders, psychosis and delirium: systemic review-based recommendations - guideline “Parkinson’s disease” of the German Society of Neu... by Karsten Witt, Johannes Levin, Thilo van Eimeren, Alkomiet Hasan, Georg Ebersbach, Mathias Bähr, Jos S. Becktepe, Daniela Berg, Kathrin Brockmann, Carsten Buhmann, Andrés Ceballos-Baumann, Joseph Claßen, Cornelius Deuschl, Günther Deuschl, Richard Dodel, Georg Ebersbach, Carsten Eggers, Thilo van Eimeren, Alessandra Fanciulli, Bruno Fimm, Ann‐Kristin Folkerts, Madeleine Gausepohl, Alkomiet Hasan, Wiebke Hermann, Rüdiger Hilker-Roggendorf, Günter U. Höglinger, Matthias Höllerhage, Franziska Hopfner, Wolfgang H. Jost, Elke Kalbe, Jan Kassubek, Stephan Klebe, Christine Klein, Martin Klietz, Thomas Köglsperger, Andrea A. Kühn, Paul Krack, Florian Krismer, Gregor Kuhlenbäumer, Johannes Levin, Inga Liepelt‐Scarfone, Paul Lingor, Kai F. Loewenbrück, Matthias Löhle, Stefan Lorenzl, Sylvia Maaß, Walter Maetzler, Regina Menzel, Philipp T. Meyer, Brit Mollenhauer, Manuela Neumann, Per Odin, Tiago F. Outeiro, Monika Pötter‐Nerger, René Reese, Kathrin Reetz, Olaf Rieß, Viktoria Ruf, Anja Schneider, Christoph Schrader, Alfons Schnitzler, Klaus Seppi, Friederike Sixel‐Döring, Alexander Storch, Lars Tönges, C. Trenkwalder, Thilo van Eimeren, Uwe Walter, Tobias Wächter, Tobias Warnecke, Florian Wegner, Christian Winkler, Karsten Witt, Dirk Woitalla, Kirsten E. Zeuner, Martina Bantel, Jonas L. Witt

    Published 2024
    Get full text
    Artigo
    Save to List
    Saved in:
  19. 19
    Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism

    Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism by Anna Helgadóttir, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Hilma Hólm, Riyaz S. Patel, Þórarinn Guðnason, Gregory T. Jones, André M. van Rij, Danny J. Eapen, Annette F. Baas, David‐Alexandre Trégouët, Pierre‐Emmanuel Morange, Joseph Emmerich, Bengt Lindblad, Anders Gottsäter, Lambertus A. Kiemeny, Jes S. Lindholt, Natzi Sakalihasan, Robert E. Ferrell, David J. Carey, James R. Elmore, Philip S. Tsao, Niels Grarup, Torben Jørgensen, Daniel R. Witte, Torben Hansen, Oluf Pedersen, Roberto Pola, Eleonora Gaetani, Hulda B. Magnadottir, Cisca Wijmenga, Gerard Tromp, Antti Ronkainen, Ynte M. Ruigrok, Jan D. Blankensteijn, Thomas Mueller, Philip S. Wells, Javier Corral, José Manuel Soria, Juan Carlos Souto, John F. Peden, Shapour Jalilzadeh, Bongani M. Mayosi, Bernard Keavney, Rona J. Strawbridge, Maria Sabater‐Lleal, Karl Gertow, Damiano Baldassarre, Kristiina Nyyssönen, Rainer Rauramaa, Andries J. Smit, Elmo Mannarino, Philippe Giral, Elena Tremoli, Ulf dé Fairé, Steve E. Humphries, Anders Hamsten, Vilhelmína Haraldsdóttir, Ísleifur Ólafsson, Magnús K. Magnússon, Nilesh J. Samani, Allan I. Levey, Hugh S. Markus, Konstantinos Kostulas, Martin Dichgans, Kenneth I. Berger, Gregor Kuhlenbäumer, E. Bernd Ringelstein, Monika Stoll, Udo Seedorf, Peter M. Rothwell, Janet T. Powell, Helena Kuivaniemi, Páll T. Önundarson, Einar Már Valdimarsson, Stefán E. Matthíasson, Daníel F. Guðbjartsson, Guðmundur Þorgeirsson, Arshed A. Quyyumi, Hugh Watkins, Martin Farrall, Unnur Þorsteinsdóttir, Kāri Stefánsson

    Published 2012
    Get full text
    Revisão
    Save to List
    Saved in:
  20. 20
    Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies

    Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies by Matthew Traylor, Martin Farrall, Elizabeth G. Holliday, Cathie Sudlow, Jemma C. Hopewell, Yu‐Ching Cheng, Myriam Fornage, M. Arfan Ikram, Rainer Malik, Steve Bevan, Unnur Þorsteinsdóttir, Mike A. Nalls, W. T. Longstreth, Kerri L. Wiggins, Sunaina Yadav, Eugenio Parati, Anita L. DeStefano, Bradford B. Worrall, Steven J. Kittner, Muhammad Saleem Khan, Alex P. Reiner, Anna Helgadóttir, Sefanja Achterberg, Israel Fernández‐Cadenas, Shérine Abboud, Reinhold Schmidt, James Walters, Wei‐Min Chen, E. Bernd Ringelstein, Martin O’Donnell, Weang-Kee Ho, Joanna Pera, Robin Lemmens, Bo Norrving, Peter Higgins, Marianne Benn, Michèle M. Sale, Gregor Kuhlenbäumer, Alex S. F. Doney, Astrid M. Vicente, Hossein Delavaran, Ale Algra, Gail Davies, Sofia A. Oliveira, Colin N. A. Palmer, Ian J. Deary, Helena Schmidt, Massimo Pandolfo, Joan Montaner, Cara L. Carty, Paul I. W. de Bakker, Konstantinos Kostulas, José M. Ferro, Natalie R. van Zuydam, Einar Már Valdimarsson, Børge G. Nordestgaard, Cecilia M. Lindgren, Vincent Thijs, Agnieszka Słowik, Danish Saleheen, Guillaume Paré, Klaus Berger, Guðmar Þorleifsson, Albert Hofman, Thomas H. Mosley, Braxton D. Mitchell, Karen L. Furie, Robert Clarke, Christopher Levi, Sudha Seshadri, Andreas Gschwendtner, Giorgio B. Boncoraglio, Pankaj Sharma, Joshua C. Bis, Sólveig Grétarsdóttir, Bruce M. Psaty, Peter M. Rothwell, Jonathan Rosand, James F. Meschia, Kāri Stefánsson, Martin Dichgans, Hugh S. Markus

    Published 2012
    Get full text Get full text
    Revisão
    Save to List
    Saved in:

Search Tools: