Výsledky vyhledávání - Sara Ortega‐Cubero

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  1. 1
    Frontobasal gray matter loss is associated with the TREM2 p.R47H variant

    Frontobasal gray matter loss is associated with the TREM2 p.R47H variant Autor Elkin O. Luís, Sara Ortega‐Cubero, Isabel Lamet, Cristina Razquín, Carlos Cruchaga, Bruno A. Benítez, Elena Lorenzo, Jaione Irigoyen, María A. Pastor, Pau Pástor

    Vydáno 2014
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  2. 2
    Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson’s Disease

    Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson’s Disease Autor Bruno A. Benítez, Albert A. Davis, Sheng Chih Jin, Laura Ibáñez, Sara Ortega‐Cubero, Pau Pástor, Jiyoon Choi, Breanna Cooper, Joel S. Perlmutter, Carlos Cruchaga

    Vydáno 2016
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  3. 3
    Automated <scp>N</scp>euromelanin <scp>I</scp>maging as a <scp>D</scp>iagnostic <scp>B</scp>iomarker for <scp>P</scp>arkinson's <scp>D</scp>isease

    Automated <scp>N</scp>euromelanin <scp>I</scp>maging as a <scp>D</scp>iagnostic <scp>B</scp>iomarker for <scp>P</scp>arkinson's <scp>D</scp>isease Autor Gabriel Castellanos, María A. Fernández‐Seara, Oswaldo Lorenzo‐Betancor, Sara Ortega‐Cubero, Marc Puigvert, Javier Uranga, Marta Vidorreta, Jaione Irigoyen, Elena Lorenzo, Arrate Muñoz‐Barrutia, Carlos Ortíz-de-Solórzano, Pau Pástor, María A. Pastor

    Vydáno 2015
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  4. 4
    Missense mutations in<i>TENM4</i>, a regulator of axon guidance and central myelination, cause essential tremor

    Missense mutations in<i>TENM4</i>, a regulator of axon guidance and central myelination, cause essential tremor Autor Hyun Hor, Ludmila Francescatto, Luca Bartesaghi, Sara Ortega‐Cubero, Maria Kousi, Oswaldo Lorenzo‐Betancor, Félix Javier Jiménez‐Jiménez, Alexandre Gironell, Jordi Clarimón, Oliver Drechsel, José A. G. Agúndez, Daniela Kenzelmann Brož, Ruth Chiquet‐Ehrismann, Alberto Lleó, F. Coria, Elena García‐Martín, Hortensia Alonso‐Navarro, M. J. Martí, Jaime Kulisevsky, Charlotte N. Hor, Stephan Ossowski, Roman Chrast, Nicholas Katsanis, Pau Pástor, Xavier Estivill

    Vydáno 2015
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  5. 5
    Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia

    Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia Autor Oriol Dols‐Icardo, Alberto García‐Redondo, Ricard Rojas‐García, Raquel Sánchez‐Valle, Antoni Noguera‐Julián, Estrella Gómez‐Tortosa, Pau Pástor, Isabel de la Torre Díez, Jesús Esteban‐Pérez, Marc Suárez‐Calvet, Sofía Antón‐Aguirre, G. Amer, Sara Ortega‐Cubero, Rafael Blesa, Juan Fortea, Daniel Alcolea, Antoni Capdevila, Anna Antonell, Albert Lladó, José Luís Muñoz-Blanco, Jesús S. Mora, Lucia Galán-Dávila, Francisco Javier Rodríguez de Rivera Garrido, Alberto Lleó, Jordi Clarimón

    Vydáno 2013
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  6. 6
    A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease

    A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease Autor Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, Sebastiaan Engelborghs, Raquel Sánchez‐Valle, Albert Lladó, Caroline Graff, Håkan Thonberg, Pau Pástor, Sara Ortega‐Cubero, María A. Pastor, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Jordi Clarimón, Alberto Lleó, Juan Fortea, Alexandre de Mendonça, Madalena Martins, Oriol Grau‐Rivera, Ellen Gelpí, Karolien Bettens, Ligia Mateiu, Lubina Dillen, Patrick Cras, Peter Paul De Deyn, Christine Van Broeckhoven, Kristel Sleegers

    Vydáno 2016
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  7. 7
    Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

    Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia Autor Agustı́n Ruiz, Oriol Dols‐Icardo, María J. Bullido, Pau Pástor, Eloy Rodríguez‐Rodríguez, Adolfo López de Munain, Marian M. de Pancorbo, Jordi Pérez‐Tur, Victoria Álvarez, Anna Antonell, Jesús López‐Arrieta, Isabel de la Torre Díez, Lluís Tárraga, Merçé Boada, Alberto Lleó, Rafael Blesa, Ana Frank, Isabel Sastre, Cristina Razquín, Sara Ortega‐Cubero, Elena Lorenzo, Pascual Sánchez‐Juan, Onofre Combarros, Fermín Moreno, Ana Gorostidi, Xabier Elcoroaristizabal, Miquel Baquero, Eliécer Coto, Raquel Sánchez‐Valle, Jordi Clarimón

    Vydáno 2013
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  8. 8
    Analysis of the<i>CHCHD10</i>gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

    Analysis of the<i>CHCHD10</i>gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain Autor Oriol Dols‐Icardo, Irene Nebot, Ana Gorostidi, Sara Ortega‐Cubero, Isabel de la Torre Díez, Ricard Rojas‐García, Alberto García‐Redondo, Mònica Povedano, Albert Lladó, Victoria Álvarez, Pascual Sánchez‐Juan, Julio Pardo, Ivonne Jericó, Juan F. Vázquez‐Costa, Teresa Sevilla, Fernando Cardona, Begoña Indakoechea, Fermín Moreno, Roberto Fernández‐Torrón, Laia Muñoz, Sonia Moreno‐Grau, Maiteé Rosende‐Roca, Álvaro Vela, José Luís Muñoz-Blanco, Onofre Combarros, Eliécer Coto, Daniel Alcolea, Juan Fortea, Alberto Lleó, Raquel Sánchez‐Valle, Jesús Esteban‐Pérez, Agustı́n Ruiz, Pau Pástor, Adolfo López de Munaín, Jordi Pérez‐Tur, Jordi Clarimón

    Vydáno 2015
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  9. 9
    Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

    Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies Autor José Brás, Rita Guerreiro, Lee Darwent, Laura Parkkinen, Olaf Ansorge, Valentina Escott‐Price, Dena G. Hernandez, Michael A. Nalls, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Wiesje M. van der Flier, Afina W. Lemstra, Philip Scheltens, Ekaterina Rogaeva, Peter St George–Hyslop, Elisabet Londos, Henrik Zetterberg, Sara Ortega‐Cubero, Pau Pástor, Tanis J. Ferman, Caroline Graff, Owen A. Ross, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Walter Maetzler, Daniela Berg, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Yaroslau Compta, Tamás Révész, Andrew J. Lees, Nigel J. Cairns, Glenda M. Halliday, David Mann, Stuart Pickering‐Brown, Dennis W. Dickson, Andrew Singleton, John Hardy

    Vydáno 2014
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  10. 10
    Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

    Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease Autor Arne De Roeck, Tobi Van den Bossche, Julie van der Zee, Jan Verheijen, Wouter De Coster, Jasper Van Dongen, Lubina Dillen, Yalda Baradaran‐Heravi, Bavo Heeman, Raquel Sánchez‐Valle, Albert Lladó, Benedetta Nacmias, Sandro Sorbi, Ellen Gelpí, Oriol Grau‐Rivera, Estrella Gómez‐Tortosa, Pau Pástor, Sara Ortega‐Cubero, María A. Pastor, Caroline Graff, Håkan Thonberg, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Alexandre de Mendonça, Madalena Martins, Barbara Borroni, Alessandro Padovani, Maria Rosário Almeida, Isabel Santana, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Jordi Clarimón, Alberto Lleó, Juan Fortea, Magda Tsolaki, Maria Koutroumani, Radoslav Matěj, Zdeněk Rohan, Peter Paul De Deyn, Sebastiaan Engelborghs, Patrick Cras, Christine Van Broeckhoven, Kristel Sleegers

    Vydáno 2017
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  11. 11
    Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

    Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases Autor Rita Guerreiro, Valentina Escott‐Price, Lee Darwent, Laura Parkkinen, Olaf Ansorge, Dena G. Hernandez, Michael A. Nalls, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Wiesje M. van der Flier, Henne Holstege, Eva Louwersheimer, Afina W. Lemstra, Philip Scheltens, Ekaterina Rogaeva, Peter St George–Hyslop, Elisabet Londos, Henrik Zetterberg, Sara Ortega‐Cubero, Pau Pástor, Tanis J. Ferman, Caroline Graff, Owen A. Ross, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Walter Maetzler, Daniela Berg, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Yaroslau Compta, Tamás Révész, Andrew J. Lees, Nigel J. Cairns, Glenda M. Halliday, David Mann, Stuart Pickering‐Brown, John Powell, Katie Lunnon, Michelle K. Lupton, Dennis W. Dickson, John Hardy, Andrew Singleton, José Brás

    Vydáno 2015
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  12. 12
    Genome-wide association study in essential tremor identifies three new loci

    Genome-wide association study in essential tremor identifies three new loci Autor 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

    Vydáno 2016
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  13. 13
    Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

    Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration Autor Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, Philip Van Damme, Céline Merlin, Annelies Laureys, Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Frederico Simões do Couto, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Caroline Graff, Huei-Hsin Chiang, Håkan Thonberg, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Giovanni B. Frisoni, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Tobias B. Haack, Tim M. Strom, Holger Prokisch, Oriol Dols‐Icardo, Jordi Clarimón, Alberto Lleó, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Michael T. Heneka, Frank Jessen, Alfredo Ramı́rez, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobková, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Thomas Ströbel, Patrick Santens, Wim Robberecht, Peter De Jonghe, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Kristel Sleegers, Christine Van Broeckhoven

    Vydáno 2014
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  14. 14
    <i>TBK1</i> Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

    <i>TBK1</i> Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis Autor Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker, Jonathan Baets, Ellen Gelpí, Ricardo Rojas-García, Jordi Clarimón, Alberto Lleó, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Robert Perneczky, Matthis Synofzik, Jennifer Just, Lüdger Schöls, Caroline Graff, Håkan Thonberg, Barbara Borroni, Alessandro Padovani, Albena Jordanova, Stayko Sarafov, Ivailo Tournev, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Frederico Simões do Couto, Alfredo Ramı́rez, Frank Jessen, Michael T. Heneka, Estrella Gómez‐Tortosa, Adrian Danek, Patrick Cras, Rik Vandenberghe, Peter De Jonghe, Peter Paul De Deyn, Kristel Sleegers, Marc Cruts, Christine Van Broeckhoven, Johan Goeman, Dirk Nuytten, Katrien Smets, Wim Robberecht, Philip Van Damme, Jan De Bleecker, Patrick Santens, Bart Dermaut, Jan Versijpt, Alex Michotte, Adrian Ivanoiu, Olivier Deryck, Bruno Bergmans, Jean Delbeck, M. Bruyland, Christiana Willems, Éric Salmon, Pau Pástor, Sara Ortega‐Cubero, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Raquel Sánchez‐Valle, Albert Lladó, Isabel Santana, Maria Rosário Almeida, Giovanni B. Frisoni, Walter Maetzler, Radoslav Matěj, Matthew J. Fraidakis, Gábor G. Kovács, Gian Maria Fabrizi, Silvia Testi

    Vydáno 2016
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  15. 15
    Frontotemporal dementia and its subtypes: a genome-wide association study

    Frontotemporal dementia and its subtypes: a genome-wide association study Autor Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, William S. Brooks, Peter R. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, María Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George‐Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim Van Langenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri, Jørgen E. Nielsen, Lena E. Hjermind, Markus J. Riemenschneider, Manuel Mayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N. Rossor

    Vydáno 2014
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  16. 16
    Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

    Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS Autor Erdogan Taskesen, Aniket Mishra, Sophie van der Sluis, Raffaele Ferrari, D. G. Hernandez, M. A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, Peter R. Schofield, Glenda M. Halliday, J. R. Hodges, Olivier Piguet, Lauren Bartley, Emma E. Thompson, Eric Haan, Israel Alejandro Quijano-Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Diego Albani, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, María Landqvist Waldö, Kristina Nilsson, Christer Nilsson, I. R. A. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Andrea Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George‐Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, J. Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Julie van der Zee, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Leber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri, Jens Høiriis Nielsen, L. E. Hjermind, Markus J. Riemenschneider, Manuel Mayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N. Rossor

    Vydáno 2017
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  17. 17
    CXCR4 involvement in neurodegenerative diseases

    CXCR4 involvement in neurodegenerative diseases Autor Luke W. Bonham, Celeste M. Karch, Chun Chieh Fan, Chin Hong Tan, Ethan G. Geier, Yunpeng Wang, Natalie Wen, Iris Broce, Yi Li, Matthew J. Barkovich, Raffaele Ferrari, John Hardy, Parastoo Momeni, Günter U. Höglinger, Ulrich Müller, Christopher P. Hess, Leo P. Sugrue, William P. Dillon, Gerard D. Schellenberg, Bruce L. Miller, Ole A. Andreassen, Anders M. Dale, A. James Barkovich, Jennifer S. Yokoyama, Rahul S. Desikan, Raffaele Ferrari, D. G. Hernandez, Mike A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, Peter R. Schofield, Glenda M. Halliday, J. R. Hodges, Olivier Piguet, Lauren Bartley, E. Aubrey Thompson, Eric Haan, Ivó H. Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, N.J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Diego Albani, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, María Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George–Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, V.M. Van Deerlin, Murray Grossman

    Vydáno 2018
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  18. 18
    Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia Autor Vivek Swarup, Flora I. Hinz, Jessica E. Rexach, K Noguchi, Hiroyoshi Toyoshiba, Akira Oda, Keisuke Hirai, Arjun Sarkar, Nicholas T. Seyfried, Chialin Cheng, Stephen J. Haggarty, Raffaele Ferrari, Jonathan D. Rohrer, Adaikalavan Ramasamy, John Hardy, Dena Hernandez, Mike A. Nalls, Andrew B. Singleton, John B. Kwok, Carol Dobson‐Stone, William S. Brooks, Peter R. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Nigel J. Cairns, Carlos Cruchaga, Giuliano Binetti, Roberta Ghidoni, Luisa Benussi, Gianluigi Forloni, Diego Albani, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, María Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David M. A. Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Evelyn Jaros, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Michael Tierney, Atik Baborie, Pau Pástor, Sara Ortega‐Cubero, Cristina Razquín, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George–Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Stuart Pickering‐Brown, Parastoo Momeni, Julie van der Zee, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Leber, Alexis Brice, Didier Hannequin, Véronique Golfier

    Vydáno 2018
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  19. 19
    Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

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    Vydáno 2022
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