Resultados da busca - Iris E. Jansen

Refinar Resultados
  1. 1
    The genetic overlap between Alzheimer’s disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson’s disease

    The genetic overlap between Alzheimer’s disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson’s disease por Douglas P. Wightman, Jeanne E. Savage, Elleke Tissink, Cato Romero, Iris E. Jansen, Daniëlle Posthuma

    Publicado em 2023
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  2. 2
    Disentangling Genetic Risks for Metabolic Syndrome

    Disentangling Genetic Risks for Metabolic Syndrome por Eva S. van Walree, Iris E. Jansen, Nathaniel Y. Bell, Jeanne E. Savage, Christiaan de Leeuw, Max Nieuwdorp, Sophie van der Sluis, Daniëlle Posthuma

    Publicado em 2022
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  3. 3
    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects

    The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects por Cornelis Blauwendraat, Carlo Wilke, Javier Simón‐Sánchez, Iris E. Jansen, Anika Reifschneider, Anja Capell, Christian Haass, Melissa Castillo-Lizardo, Saskia Biskup, Walter Maetzler, Patrizia Rizzu, Peter Heutink, Matthis Synofzik

    Publicado em 2017
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  4. 4
    Immune response and endocytosis pathways are associated with the resilience against Alzheimer’s disease

    Immune response and endocytosis pathways are associated with the resilience against Alzheimer’s disease por Niccoló Tesi, Sven J. van der Lee, Marc Hulsman, Iris E. Jansen, Najada Stringa, Natasja M. van Schoor, Philip Scheltens, Wiesje M. van der Flier, Martijn Huisman, Marcel J. T. Reinders, Henne Holstege

    Publicado em 2020
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  5. 5
    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease

    Centenarian controls increase variant effect sizes by an average twofold in an extreme case–extreme control analysis of Alzheimer’s disease por Niccoló Tesi, Sven J. van der Lee, Marc Hulsman, Iris E. Jansen, Najada Stringa, Natasja M. van Schoor, Hanne Meijers‐Heijboer, Martijn Huisman, Philip Scheltens, Marcel J. T. Reinders, Wiesje M. van der Flier, Henne Holstege

    Publicado em 2018
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  6. 6
    Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

    Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's por Ganqiang Liu, Brendon Boot, Joseph J. Locascio, Iris E. Jansen, Sophie Winder‐Rhodes, Shirley Eberly, Alexis Elbaz, Alexis Brice, Bernard Ravina, Jacobus J. van Hilten, Florence Cormier‐Dequaire, Jean‐Christophe Corvol, Roger A. Barker, Peter Heutink, Johan Marinus, Caroline H. Williams‐Gray, Clemens R. Scherzer

    Publicado em 2016
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  7. 7
    Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

    Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance por Steven Lubbe, Valentina Escott‐Price, J. Raphael Gibbs, Mike A. Nalls, José Brás, T. Ryan Price, Aude Nicolas, Iris E. Jansen, Kin Y. Mok, Alan Pittman, James E. Tomkins, Patrick A. Lewis, Alastair Noyce, Suzanne Lesage, Manu Sharma, Elena Schiff, Adam P. Levine, Alexis Brice, Thomas Gasser, John Hardy, Peter Heutink, Nicholas Wood, Andrew Singleton, Nigel Williams, Huw R. Morris

    Publicado em 2016
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  8. 8
    Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

    Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases por Aree Witoelar, Iris E. Jansen, Yunpeng Wang, Joshua Shulman, J. Raphael Gibbs, Cornelis Blauwendraat, Wesley K. Thompson, Dena G. Hernandez, Srdjan Djurovic, Andrew J. Schork, Francesco Bettella, David Ellinghaus, Andre Franke, Benedicte A. Lie, Linda K. McEvoy, Tom H. Karlsen, Suzanne Lesage, Huw R. Morris, Alexis Brice, Nicholas Wood, Peter Heutink, John Hardy, Andrew B. Singleton, Anders M. Dale, Thomas Gasser, Ole A. Andreassen, Manu Sharma

    Publicado em 2017
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  9. 9
    Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing

    Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing por Iris E. Jansen, Hui Ye, Sasja Heetveld, Marie C. Lechler, Helen Michels, Renée I. Seinstra, Steven Lubbe, Valérie Drouet, Suzanne Lesage, Elisa Majounie, J. Raphael Gibbs, Mike A. Nalls, Mina Ryten, Juan A. Botía, Jana Vandrovcová, Javier Simón‐Sánchez, Melissa Castillo-Lizardo, Patrizia Rizzu, Cornelis Blauwendraat, Amit K. Chouhan, Yarong Li, Puja Yogi, Najaf Amin, Cornelia M. van Duijn, Huw R. Morris, Alexis Brice, Andrew Singleton, Della David, Ellen A. A. Nollen, Shushant Jain, Joshua Shulman, Peter Heutink

    Publicado em 2017
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  10. 10
    NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

    NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases por Mike A. Nalls, José Brás, Dena G. Hernandez, Margaux F. Keller, Elisa Majounie, Alan E. Renton, Mohamad Saad, Iris E. Jansen, Rita Guerreiro, Steven Lubbe, Vincent Plagnol, J. Raphael Gibbs, Claudia Schulte, Nathan Pankratz, Margaret Sutherland, Lars Bertram, Christina M. Lill, Anita L. DeStefano, Tatiana Faroud, Nicholas Eriksson, Joyce Y. Tung, Connor Edsall, Noah Nichols, Janet Brooks, Sampath Arepalli, Hannah A. Pliner, Christopher T. Letson, Peter Heutink, María Martínez, Thomas Gasser, Bryan J. Traynor, Nicholas Wood, John Hardy, Andrew Singleton

    Publicado em 2014
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  11. 11
    Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer’s disease

    Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer’s disease por Iris Broce, Chin Hong Tan, Chun Chieh Fan, Iris E. Jansen, Jeanne E. Savage, Aree Witoelar, Natalie Wen, Christopher P. Hess, William P. Dillon, Christine M. Glastonbury, M. Maria Glymour, Jennifer S. Yokoyama, Fanny M. Elahi, Gil D. Rabinovici, Bruce L. Miller, Elizabeth C. Mormino, Reisa A. Sperling, David A. Bennett, Linda K. McEvoy, James B. Brewer, Howard Feldman, Bradley T. Hyman, Margaret A. Pericak‐Vance, Jonathan L. Haines, Lindsay A. Farrer, Richard Mayeux, Gerard D. Schellenberg, Kristine Yaffe, Leo P. Sugrue, Anders M. Dale, Daniëlle Posthuma, Ole A. Andreassen, Celeste M. Karch, Rahul S. Desikan

    Publicado em 2018
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  12. 12
    Cerebrospinal fluid tau levels are associated with abnormal neuronal plasticity markers in Alzheimer’s disease

    Cerebrospinal fluid tau levels are associated with abnormal neuronal plasticity markers in Alzheimer’s disease por Pieter Jelle Visser, Lianne M. Reus, Johan Gobom, Iris E. Jansen, Ellen Dicks, Sven J. van der Lee, Magda Tsolaki, Frans R.J. Verhey, Julius Popp, Pablo Martínez‐Lage, Rik Vandenberghe, Alberto Lleó, José Luís Molinuevo, Sebastiaan Engelborghs, Yvonne Freund‐Levi, Lutz Froelich, Kristel Sleegers, Valerija Dobričić, Simon Lovestone, Johannes Streffer, Stephanie J. B. Vos, Isabelle Bos, August B. Smit, Kaj Blennow, Philip Scheltens, Charlotte E. Teunissen, Lars Bertram, Henrik Zetterberg, Betty M. Tijms, August B. Smit, Kaj Blennow, Philip Scheltens, Charlotte E. Teunissen, Lars Bertram, Henrik Zetterberg, Betty M. Tijms

    Publicado em 2022
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  13. 13
    Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk

    Genetic meta-analysis identifies 9 novel loci and functional pathways for Alzheimer’s disease risk por Iris E. Jansen, Jeanne E. Savage, Kyoko Watanabe, Julien Bryois, Dylan M. Williams, Stacy Steinberg, Julia Sealock, Ida Karlsson, Sara Hägg, Lavinia Athanasiu, Nicola Voyle, Petroula Proitsi, Aree Witoelar, Sven Stringer, Dag Aarsland, Ina S. Almdahl, Fred Andersen, Sverre Bergh, Francesco Bettella, Sigurbjörn Björnsson, Anne Brækhus, Geir Bråthen, Christiaan de Leeuw, Rahul S. Desikan, Srdjan Djurovic, Logan Dumitrescu, Tormod Fladby, Timothy Homan, Pálmi V. Jónsson, Steven J. Kiddle, K Arvid Rongve, Ingvild Saltvedt, Sigrid Botne Sando, Geir Selbæk, Nathan Skenne, Jón Snædal, Eystein Stordal, Ingun Ulstein, Yunpeng Wang, Linda R. White, Jens Hjerling‐Leffler, Patrick F. Sullivan, Wiesje M. van der Flier, Richard Dobson, Lea K. Davis, Hreinn Stefánsson, Kāri Stefánsson, Nancy L. Pedersen, Stephan Ripke, Ole A. Andreassen, Daniëlle Posthuma

    Publicado em 2018
    Obter o texto integral Obter o texto integral
    Pré-impressão
    Salvar na lista
    Na minha lista:
  14. 14
    Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk

    Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk por Iris E. Jansen, Jeanne E. Savage, Kyoko Watanabe, Julien Bryois, Dylan M. Williams, Stacy Steinberg, Julia Sealock, Ida Karlsson, Sara Hägg, Lavinia Athanasiu, Nicola Voyle, Petroula Proitsi, Aree Witoelar, Sven Stringer, Dag Aarsland, Ina S. Almdahl, Fred Andersen, Sverre Bergh, Francesco Bettella, Sigurbjörn Björnsson, Anne Brækhus, Geir Bråthen, Christiaan de Leeuw, Rahul S. Desikan, Srdjan Djurovic, Logan Dumitrescu, Tormod Fladby, Timothy J. Hohman, Pálmi V. Jónsson, Steven J. Kiddle, Arvid Rongve, Ingvild Saltvedt, Sigrid Botne Sando, Geir Selbæk, Maryam Shoai, Nathan Skene, Jón Snædal, Eystein Stordal, Ingun Ulstein, Yunpeng Wang, Linda R. White, John Hardy, Jens Hjerling‐Leffler, Patrick F. Sullivan, Wiesje M. van der Flier, Richard Dobson, Lea K. Davis, Hreinn Stefánsson, Kāri Stefánsson, Nancy L. Pedersen, Stephan Ripke, Ole A. Andreassen, Daniëlle Posthuma

    Publicado em 2019
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  15. 15
    PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment

    PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment por Luca Kleineidam, Vincent Chouraki, Tomasz Próchnicki, Sven J. van der Lee, Laura Madrid, Holger Wagner-Thelen, Ilker Karaca, Leonie Weinhold, Steffen Wolfsgruber, Anne Boland, Pamela V. Martino Adami, Piotr Lewczuk, Julius Popp, Frederic Brosseron, Iris E. Jansen, Marc Hulsman, Johannes Kornhuber, Oliver Peters, Claudine Berr, Reinhard Heun, Lutz Frölich, Christophe Tzourio, Jean‐François Dartigues, Michael Hüll, Ana Espinosa, Isabel Hernández, Itziar de Rojas, Adelina Orellana, Sergi Valero, Najada Stringa, Natasja M. van Schoor, Martijn Huisman, Philip Scheltens, for the Alzheimer’s Disease Neuroimaging Initiative, Eckart Rüther, Jean‐François Deleuze, Jens Wiltfang, Lluís Tárraga, Matthias Schmid, Martin Scherer, Steffi G. Riedel‐Heller, Michael T. Heneka, Philippe Amouyel, Frank Jessen, Merçé Boada, Wolfgang Maier, Anja Schneider, Antonio González-Pérez, Wiesje M. van der Flier, Michael Wagner, Jean‐Charles Lambert, Henne Holstege, María Eugenia Sáez, Eicke Latz, Agustı́n Ruiz, Alfredo Ramı́rez

    Publicado em 2020
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  16. 16
    Largest GWAS (N=1,126,563) of Alzheimer’s Disease Implicates Microglia and Immune Cells

    Largest GWAS (N=1,126,563) of Alzheimer’s Disease Implicates Microglia and Immune Cells por Douglas P. Wightman, Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Arvid Rongve, Sigrid Børte, Bendik S Winsvold, Ole Kristian Drange, Amy E. Martinsen, Anne Heidi Skogholt, Cristen J. Willer, Geir Bråthen, Ingunn Bosnes, Jonas B. Nielsen, Lars G. Fritsche, Laurent F. Thomas, Linda M. Pedersen, Maiken E. Gabrielsen, Marianne Bakke Johnsen, Tore Wergeland Meisingset, Wei Zhou, Petroula Proitsi, Angela Hodges, Richard Dobson, Latha Velayudhan, Julia Sealock, Lea K. Davis, Nancy L. Pedersen, Chandra A. Reynolds, Ida Karlsson, Sigurður H. Magnússon, Hreinn Stefánsson, Steinunn Þórðardóttir, Pálmi V. Jónsson, Jón Snædal, Anna Zettergren, Ingmar Skoog, Silke Kern, Margda Wærn, Henrik Zetterberg, Kaj Blennow, Eystein Stordal, Kristian Hveem, John‐Anker Zwart, Lavinia Athanasiu, Ingvild Saltvedt, Sigrid Botne Sando, Ingun Ulstein, Srdjan Djurovic, Tormod Fladby, Dag Aarsland, Geir Selbæk, Stephan Ripke, Kāri Stefánsson, Ole A. Andreassen, Daniëlle Posthuma

    Publicado em 2020
    Obter o texto integral
    Pré-impressão
    Salvar na lista
    Na minha lista:
  17. 17
    A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

    A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD por Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chió, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor

    Publicado em 2011
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  18. 18
    A meta-analysis of genome-wide association studies identifies multiple longevity genes

    A meta-analysis of genome-wide association studies identifies multiple longevity genes por Joris Deelen, Daniel S. Evans, Dan E. Arking, Niccoló Tesi, Marianne Nygaard, Xiaomin Liu, Mary K. Wojczynski, Mary L. Biggs, Ashley van der Spek, Gil Atzmon, Erin B. Ware, Chloé Sarnowski, Albert V. Smith, Ilkka Seppälä, Heather J. Cordell, Janina Dose, Najaf Amin, Alice M. Arnold, Kristin L. Ayers, Nir Barzilai, Elizabeth J. Becker, Marian Beekman, Hélène Blanché, Kaare Christensen, Lene Christiansen, Joanna Collerton, Sarah Cubaynes, Steven R. Cummings, Karen Davies, Birgit Debrabant, Jean‐François Deleuze, Rachel Duncan, Jessica D. Faul, Claudio Franceschi, Pilar Galán, Vilmundur Guðnason, Tamara B. Harris, Martijn Huisman, Mikko Hurme, Carol Jagger, Iris E. Jansen, Marja Jylhä, Mika Kähönen, David Karasik, Sharon L. R. Kardia, Andrew Kingston, Thomas B. L. Kirkwood, Lenore J. Launer, Terho Lehtimäki, Wolfgang Lieb, Leo‐Pekka Lyytikäinen, Carmen Martin‐Ruiz, Junxia Min, Almut Nebel, Anne B. Newman, Chao Nie, Ellen A. Nøhr, Eric Orwoll, Thomas T. Perls, Michael A. Province, Bruce M. Psaty, Olli Raitakari, Marcel J. T. Reinders, Jean‐Marie Robine, Jerome I. Rotter, Paola Sebastiani, Jennifer A. Smith, Thorkild I. A. Sørensen, Kent D. Taylor, André G. Uitterlinden, Wiesje M. van der Flier, Sven J. van der Lee, Cornelia M. van Duijn, Alan B. Zonderman, James W. Vaupel, David R. Weir, Kenny Ye, Yi Zeng, Wanlin Zheng, Henne Holstege, Douglas P. Kiel, Kathryn L. Lunetta, P. Eline Slagboom, Joanne M. Murabito

    Publicado em 2019
    Obter o texto integral
    Revisão
    Salvar na lista
    Na minha lista:
  19. 19
    Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

    Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease por Laurie Robak, Iris E. Jansen, Jeroen van Rooij, André G. Uitterlinden, Robert Kraaij, Joseph Jankovic, Peter Heutink, Joshua Shulman, Mike A. Nalls, Vincent Plagnol, Dena G Hernandez, Manu Sharma, Una‐Marie Sheerin, Mohamad Saad, Javier Simón‐Sánchez, Claudia Schulte, Suzanne Lesage, Sigurlaug Sveinbjörnsdóttir, Sampath Arepalli, Roger A. Barker, Yoav Ben-, Henk W. Berendse, Daniela Berg, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bas R. Bloem, Zoltán Bochdanovits, Michael Bonin, José Brás, Kathrin Brockmann, Janet Brooks, David J. Burn, Elisa Majounie, Gavin Charlesworth, Codrin Lungu, Honglei Chen, Patrick F. Chinnery, Sean Chong, Carl E Clarke, Mark Cookson, Jonathan M. Cooper, Jean‐Christophe Corvol, Carl Counsell, Philippe Damier, Jean‐François Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, F. Durif, Alexandra Dürr, Sarah Edkins, Jonathan Evans, Thomas Foltynie, Jing Dong, Michelle Gardner, J. Raphael Gibbs, Alison Goate, Emma Gray, Rita Guerreiro, Clare Harris, Jacobus J. van Hilten, Albert Hofman, Albert R. Hollenbeck, Janice L. Holton, Joshua Shulman, Joshua Shulman, Isabel Wurster, Walter Mätzler, Gavin Hudson, Sarah Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Jean‐Charles Lambert, Cordelia Langford, Andrew J. Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, Delia Lorenz, Codrin Lungu, Alisdair McNeill, Catriona Moorby, Matthew Moore, Huw R. Morris, Karen Morrison, Valentina Escott‐Price, Ese Mudanohwo, Sean S. O’Sullivan, Justin Pearson, Joel S. Perlmutter, Hjörvar Pétursson, Pierre Pollak, Bart Post, Simon Potter, Bernard Ravina, Tamás Révész

    Publicado em 2017
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  20. 20
    New insights on the genetic etiology of Alzheimer’s and related dementia

    New insights on the genetic etiology of Alzheimer’s and related dementia por Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Víctor Andrade, Sonia Moreno‐Grau, Najaf Amin, Adam C. Naj, Benjamin Grenier‐Boley, Rafael Campos‐Martin, Peter Holmans, Anne Boland, Luca Kleineidam, Vincent Damotte, Sven J. van der Lee, Teemu Kuulasmaa, Qiong Yang, Itziar de Rojas, Joshua C. Bis, Amber Yaqub, Ivana Nedeljković, Marcos R. Costa, Julien Chapuis, Shahzad Ahmad, Vilmantas Giedraitis, Merçé Boada, Dag Aarsland, Pablo García‐González, Carla Abdelnour, Emilio Alarcón‐Martín, Montserrat Alegret, Ignacio Álvarez, Victoria Álvarez, Nicola J. Armstrong, Anthoula Tsolaki, Carmen Antúnez, Ildebrando Appollonio, Marina Arcaro, Silvana Archetti, Alfonso Arias Pastor, Beatrice Arosio, Lavinia Athanasiu, Henri Bailly, Nerisa Banaj, Miquel Baquero, Ana Belén Pastor, Luisa Benussi, Claudine Berr, Céline Besse, Valentina Bessi, Giuliano Binetti, Alessandra Bizzarro, Daniel Alcolea, Rafael Blesa, Barbara Borroni, Silvia Boschi, Paola Bossù, Geir Bråthen, Catherine Bresner, Keeley J. Brookes, Luis Ignacio Brusco, Katharina Bürger, María J. Bullido, Vanessa Burholt, William S. Bush, Miguel Calero, Carole Dufouil, Ángel Carracedo, Roberta Cecchetti, Laura Cervera‐Carles, Camille Charbonnier, Caterina Chillotti, Henry Brodaty, Simona Ciccone, Jurgen A.H.R. Claassen, Christopher Clark, Elisa Conti, Anaïs Corma‐Gómez, Emanuele Maria Costantini, Carlo Custodero, Delphine Daian, Carolina Dalmasso, Antonio Daniele, Efthimios Dardiotis, Jean‐François Dartigues, Peter Paul De Deyn, Kátia de Paiva Lopes, Lot D. de Witte, Stéphanie Debette, Jürgen Deckert, Teodoro del Ser, Nicola Denning, Anita L. DeStefano, Martin Dichgans, Janine Diehl‐Schmid, Mónica Díez-Fairén, Paolo Rossi, Srdjan Djurovic, Emmanuelle Duron, Emrah Düzel, Sebastiaan Engelborghs

    Publicado em 2020
    Obter o texto integral Obter o texto integral
    Pré-impressão
    Salvar na lista
    Na minha lista:

Ferramentas de busca: