Kết quả tìm kiếm - Oswaldo Lorenzo‐Betancor
- Đang hiển thị 1 - 17 kết quả của 17
-
1
Epigenetic regulation in Parkinson’s disease Bằng Catherine Labbé, Oswaldo Lorenzo‐Betancor, Owen A. Ross
Được phát hành 2016Revisão -
2
PINK1-linked parkinsonism is associated with Lewy body pathology Bằng Lluı́s Samaranch, Oswaldo Lorenzo‐Betancor, José Matías Arbelo, Isidró Ferrer, Elena Lorenzo, Jaione Irigoyen, María A. Pastor, Carmen Marrero, Concepción Isla, Joanna Herrera-Henriquez, Pau Pástor
Được phát hành 2010Artigo -
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 Bằng 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
Được phát hành 2015Artigo -
4
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru Bằng Carlos Velez‐Pardo, Oswaldo Lorenzo‐Betancor, Marlene Jiménez-Del-Río, Sonia Moreno, Francisco Lopera, Mario Cornejo‐Olivas, Luis Torres, Miguel Inca‐Martinez, Pilar Mazzetti, Carlos Cosentino, Dora Yearout, Sarah M. Waldherr, Cyrus P. Zabetian, Ignácio F. Mata
Được phát hành 2019Artigo -
5
An association study between Heme oxygenase-1 genetic variants and Parkinson's disease Bằng Pedro Ayuso, Carmen MartÃnez, Pau Pástor, Oswaldo Lorenzo‐Betancor, Antonio Luengo, Félix J. Jiménez-Jiménez, Hortensia Alonso‐Navarro, José A. G. AgÃondez, Elena GarcÃa-MartÃn
Được phát hành 2014Artigo -
6
Replication of <i>MAPT</i> and <i>SNCA</i>, but not <i>PARK16‐18</i>, as susceptibility genes for Parkinson's disease Bằng Ignácio F. Mata, Dora Yearout, Victoria Álvarez, Eliécer Coto, Lorena de Mena, Renée Ribacoba, Oswaldo Lorenzo‐Betancor, Lluı́s Samaranch, Pau Pástor, Sebastián Cervantes, Jon Infante, Inés García‐Gorostiaga, María Sierra, Onofre Combarros, Katherine W. Snapinn, Karen L. Edwards, Cyrus P. Zabetian
Được phát hành 2011Artigo -
7
Analysis of COQ2gene in multiple system atrophy Bằng Kotaro Ogaki, Shinsuke Fujioka, Michael G. Heckman, Sruti Rayaprolu, Alexandra I. Soto‐Ortolaza, Catherine Labbé, Ronald L. Walton, Oswaldo Lorenzo‐Betancor, Xue Wang, Yan W. Asmann, Rosa Rademakers, Neill R. Graff‐Radford, Ryan J. Uitti, William P. Cheshire, Zbigniew K. Wszołek, Dennis W. Dickson, Owen A. Ross
Được phát hành 2014Artigo -
8
(Patho‐)physiological relevance of <scp>PINK</scp> 1‐dependent ubiquitin phosphorylation Bằng Fabienne C. Fiesel, Maya Ando, Roman Hudec, Anneliese R. Hill, Monica Castanedes‐Casey, Thomas R. Caulfield, Elisabeth L. Moussaud-Lamodière, Jeannette N. Stankowski, Peter Bauer, Oswaldo Lorenzo‐Betancor, Isidró Ferrer, José Matías Arbelo, Joanna Siuda, Li Chen, Valina L. Dawson, Ted M. Dawson, Zbigniew K. Wszołek, Owen A. Ross, Dennis W. Dickson, Wolfdieter Springer
Được phát hành 2015Artigo -
9
Rare variants in β-Amyloid precursor protein (APP) and Parkinson’s disease Bằng Eva C. Schulte, Akio Fukumori, Brit Mollenhauer, Hyun Hor, Thomas Arzberger, Robert Perneczky, Alexander Kurz, Janine Diehl‐Schmid, Michael Hüll, Peter Lichtner, Gertrud Eckstein, Alexander Zimprich, Dietrich Haubenberger, Walter Pirker, Thomas Brücke, Benjámin Bereznai, Mária Judit Molnár, Oswaldo Lorenzo‐Betancor, Pau Pástor, Annette Peters, Christian Gieger, Xavier Estivill, Thomas Meitinger, Hans A. Kretzschmar, Claudia Trenkwalder, Christian Haass, Juliane Winkelmann
Được phát hành 2015Artigo -
10
Missense mutations in<i>TENM4</i>, a regulator of axon guidance and central myelination, cause essential tremor Bằng 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
Được phát hành 2015Artigo -
11
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease Bằng Xu Hou, Fabienne C. Fiesel, Dominika Truban, Monica Castanedes Casey, Wen-Lang Lin, Alexandra I. Soto, Paweł Tacik, Linda Rousseau, Nancy N. Diehl, Michael G. Heckman, Oswaldo Lorenzo‐Betancor, Isidró Ferrer, José Matías Arbelo, John C. Steele, Matthew J. Farrer, Mario Cornejo‐Olivas, Luis Torres, Ignácio F. Mata, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Owen A. Ross, Melissa E. Murray, Dennis W. Dickson, Wolfdieter Springer
Được phát hành 2018Artigo -
12
Dopaminergic Neuronal Imaging in Genetic Parkinson's Disease: Insights into Pathogenesis Bằng Alisdair McNeill, Ruey‐Meei Wu, Kai‐Yuan Tzen, Patrícia de Carvalho Aguiar, José Matías Arbelo, Paolo Barone, Kailash P. Bhatia, Orlando Graziani Póvoas Barsottini, Vincenzo Bonifati, Sevasti Bostantjopoulou, Rodrigo A. Bressan, Giovanni Cossu, Pietro Cortelli, André C. Felício, Henrique Ballalai Ferraz, Joanna Herrera, Henry Houlden, Marcelo Q. Hoexter, Concepción Isla, Andrew J. Lees, Oswaldo Lorenzo‐Betancor, Niccolò E. Mencacci, Pau Pástor, Sabina Pappatà, Maria Teresa Pellecchia, Laura Silveira‐Moriyama, Andrea Varrone, Thomas Foltynie, Anthony H.V. Schapira
Được phát hành 2013Artigo -
13
Mitochondrial targeting sequence variants of the <i>CHCHD2</i> gene are a risk for Lewy body disorders Bằng Kotaro Ogaki, Shunsuke Koga, Michael G. Heckman, Fabienne C. Fiesel, Maya Ando, Catherine Labbé, Oswaldo Lorenzo‐Betancor, Elisabeth L. Moussaud-Lamodière, Alexandra I. Soto‐Ortolaza, Ronald L. Walton, Audrey Strongosky, Ryan J. Uitti, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzińska, Anna Krygowska‐Wajs, Maria Barcikowska, K Czyźewski, Andreas Puschmann, Kenya Nishioka, Manabu Funayama, Nobutaka Hattori, Joseph E. Parisi, Ronald C. Petersen, Caroline Graff, Bradley F. Boeve, Wolfdieter Springer, Zbigniew K. Wszołek, Dennis W. Dickson, Owen A. Ross
Được phát hành 2015Artigo -
14
LRRK2 variation and dementia with Lewy bodies Bằng Michael G. Heckman, Alexandra I. Soto‐Ortolaza, Mónica Sánchez-Contreras, Melissa E. Murray, Otto Pedraza, Nancy N. Diehl, Ronald L. Walton, Catherine Labbé, Oswaldo Lorenzo‐Betancor, Ryan J. Uitti, Jay Van Gerpen, Nilüfer Ertekin‐Taner, Glenn E. Smith, Kejal Kantarci, Rodolfo Savica, David T. Jones, Jonathan Graff‐Radford, David S. Knopman, Val J. Lowe, Clifford R. Jack, Ronald C. Petersen, Joseph E. Parisi, Rosa Rademakers, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Tanis J. Ferman, Dennis W. Dickson, Bradley F. Boeve, Owen A. Ross
Được phát hành 2016Artigo -
15
Genome-wide association study in essential tremor identifies three new loci Bằng 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
Được phát hành 2016Artigo -
16
Association of Essential Tremor With Novel Risk Loci Bằng 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
Được phát hành 2022Revisão -
17
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease Bằng Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin, Bruno A. Benítez, Yefei Cai, Rita Guerreiro, Oscar Harari, Joanne Norton, John Budde, Sarah Bertelsen, Amanda T. Jeng, Breanna Cooper, Tara Skorupa, David Carrell, Denise Levitch, Simon Hsu, Jiyoon Choi, Mina Ryten, John Hardy, Mina Ryten, Daniah Trabzuni, Michael E. Weale, Adaikalavan Ramasamy, Colin Smith, Celeste Sassi, José Brás, J. Raphael Gibbs, Dena G. Hernandez, Michelle K. Lupton, John Powell, Paola Forabosco, Perry G. Ridge, Christopher Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ronald G. Munger, Cameron Schmutz, Maegan Leary, F. Yesim Demirci, Mikhil Bamne, Xingbin Wang, Oscar L. López, Mary Ganguli, Christopher Medway, James Turton, Jenny Lord, Anne Braae, Imelda Barber, Kristelle Brown, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, David Mann, Stuart Pickering‐Brown, Kristelle Brown, Noor Kalsheker, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes, Pau Pástor, Oswaldo Lorenzo‐Betancor, Zoran Brkanac, Erick R. Scott, Eric J. Topol, Kevin Morgan, Ekaterina Rogaeva, Andrew B. Singleton, John Hardy, M. Ilyas Kamboh, Peter St George‐Hyslop, Nigel J. Cairns, John C. Morris, John Kauwe, Alison Goate
Được phát hành 2013Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Medicine
Genetics
Disease
Internal medicine
Parkinson's disease
Pathology
Neuroscience
Lewy body
Environmental health
Genotype
LRRK2
Population
Single-nucleotide polymorphism
Genetic association
Genome-wide association study
Allele
Alpha-synuclein
Alzheimer's disease
Apoptosis
Atrophy
Biochemistry
Bioinformatics
Dementia
Demography
Essential tremor
Exon
Mutation
Parkin