Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Peter Heutink"'
Publikováno v:
Movement disorders 36(4), 832-841 (2021). doi:10.1002/mds.28387
Parkinson's disease (PD) is primarily known as a movement disorder because of typical clinical manifestations associated with the loss of dopaminergic neurons in the substantia nigra. However, it is now widely recognized that PD is a much more comple
Autor:
Mafalda Raposo, Conceição Bettencourt, Ana Rosa Vieira Melo, Ana F. Ferreira, Isabel Alonso, Paulo Silva, João Vasconcelos, Teresa Kay, Maria Luiza Saraiva-Pereira, Marta D. Costa, Daniela Vilasboas-Campos, Bruno Filipe Bettencourt, Jácome Bruges-Armas, Henry Houlden, Peter Heutink, Laura Bannach Jardim, Jorge Sequeiros, Patrícia Maciel, Manuela Lima
Publikováno v:
Neurobiology of disease 162, 105578 (2022). doi:10.1016/j.nbd.2021.105578
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Neurobiology of Disease, Vol 162, Iss, Pp 105578-(2022)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Neurobiology of Disease, Vol 162, Iss, Pp 105578-(2022)
Funding Information: This work was funded by FEDER - Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020 - Operacional Programme for Competitiveness and Internationalisation (POCI), Portugal 2020 , and by Portuguese funds through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4201fe240bc3422a5890fb54ec2ae59c
https://hdl.handle.net/10362/129676
https://hdl.handle.net/10362/129676
Autor:
Lisa M. Shulman, Hirotaka Iwaki, David A. Hinds, Jacob Gratten, Huw R. Morris, Joseph Jankovic, Costanza L. Vallerga, J. Raphael Gibbs, John Hardy, Javier Simón-Sánchez, Johan Marinus, Thomas Gasser, Peter Heutink, Alexis Brice, Andrew B. Singleton, Dena G. Hernandez, Jean-Christophe Corvol, Karl Heilbron, Donald G. Grosset, Manu Sharma, Ari Siitonen, Peter M. Visscher, Sonja W. Scholz, Pentti J. Tienari, Lynne Krohn, Mathias Toft, Manuela Tan, Johanna Eerola-Rautio, Mike A. Nalls, Jacobus J. van Hilten, Lasse Pihlstrøm, Claudia Schulte, Ziv Gan-Or, Sara Bandres-Ciga, Cornelis Blauwendraat, Hampton L. Leonard, Alastair J. Noyce, Kari Majamaa, Rainer von Coelln, N Wood, Joshua M. Shulman, Suzanne Lesage
Publikováno v:
Movement disorders 34(6), 866-875 (2019). doi:10.1002/mds.27659
Mov Disord
Movement Disorders, 34(6), 866-875
Mov Disord
Movement Disorders, 34(6), 866-875
Background Increasing evidence supports an extensive and complex genetic contribution to PD. Previous genome-wide association studies (GWAS) have shed light on the genetic basis of risk for this disease. However, the genetic determinants of PD age at
Autor:
Stefania Fedele, Francesca Persichetti, Raffaella Calligaris, Claudio Santoro, Piero Carninci, Yoshihide Hayashizaki, Silvia Zucchelli, Peter Heutink, Stefano Gustincich, Hideya Kawaji, Alistair R. R. Forrest, Timo Lassmann, Masayoshi Itoh, Patrizia Rizzu, Paolo Vatta
Publikováno v:
Molecular Neurobiology
Molecular neurobiology 56(8), 5392-5415 (2019). doi:10.1007/s12035-018-1465-2
Molecular Neurobiology, 56(8), 5392-5415. Humana Press
Zucchelli, S, Fedele, S, Vatta, P, Calligaris, R, Heutink, P, Rizzu, P, Itoh, M, Persichetti, F, Santoro, C, Kawaji, H, Lassmann, T, Hayashizaki, Y, Carninci, P, Forrest, A R R, Gustincich, S & FANTOM Consortium 2019, ' Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases ', Molecular Neurobiology, vol. 56, no. 8, pp. 5392-5415 . https://doi.org/10.1007/s12035-018-1465-2
Molecular neurobiology 56(8), 5392-5415 (2019). doi:10.1007/s12035-018-1465-2
Molecular Neurobiology, 56(8), 5392-5415. Humana Press
Zucchelli, S, Fedele, S, Vatta, P, Calligaris, R, Heutink, P, Rizzu, P, Itoh, M, Persichetti, F, Santoro, C, Kawaji, H, Lassmann, T, Hayashizaki, Y, Carninci, P, Forrest, A R R, Gustincich, S & FANTOM Consortium 2019, ' Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases ', Molecular Neurobiology, vol. 56, no. 8, pp. 5392-5415 . https://doi.org/10.1007/s12035-018-1465-2
Natural antisense transcripts are common features of mammalian genes providing additional regulatory layers of gene expression. A comprehensive description of antisense transcription in loci associated to familial neurodegenerative diseases may ident
Autor:
Manuel Mayhaus, Sandro Sorbi, Peter R. Schofield, A. Rollin, A. Karydas, Alessandro Padovani, Gilles Gasparoni, Peter St George-Hyslop, Carol Dobson-Stone, Stefano F. Cappa, D. S. Knopman, John Hardy, John R. Hodges, Graziella Milan, Florence Pasquier, Christopher Morris, Edward D. Huey, Marc Cruts, Y.A.L. Pijnenburg, R. C. Petersen, Elisa Rubino, P. Scheltens, Vincent Deramecourt, Neil Graff-Radford, Elio Scarpini, Ting Wang, Panagiotis Alexopoulos, Peter Heutink, Lena E. Hjermind, AB Singleton, Jordan Grafman, Elizabeth Thompson, Adrian Danek, Pietro Pietrini, Raffaele Ferrari, Innocenzo Rainero, C. Van Broeckhoven, Rosa Capozzo, Adaikalavan Ramasamy, J. van der Zee, Eric M. Wassermann, Karin Nilsson, Ging-Yuek Robin Hsiung, J. C. van Swieten, Ping Zeng, Rosa Rademakers, Siro Bagnoli, Amalia C. Bruni, Anna Richardson, Dimitrios Kapogiannis, Ian R. A. Mackenzie, Martin N. Rossor, Bruce L. Miller, Roberta Ghidoni, Raffaele Maletta, Massimo Franceschi, Rafael Blesa, Vivianna M. Van Deerlin, Christer Nilsson, Glenda M. Halliday, Jordi Clarimón, John Q. Trojanowski, Michael Tierney, Valeria Novelli, Agustín Ruiz, Didier Hannequin, Giorgio Giaccone, Elise G.P. Dopper, Nicoletta Smirne, F Tagliavini, I. Leber, Julie S. Snowden, Sara Rollinson, Alexis Brice, Ian G. McKeith, John E. Nielsen, Paolo Sorrentino, Véronique Golfier, Maura Gallo, Lauren Bartley, B. F. Boeve, Giancarlo Logroscino, Elena Alonso, Lorenzo Pinessi, Matt Baker, Nigel J. Cairns, Matthias Riemenschneider, William S. Brooks, Alexander Gerhard, Mark Kristiansen, Eric Haan, Israel Hernandez, Ekaterina Rogaeva, Jason D. Warren, Thibaud Lebouvier, Nick C. Fox, Stuart Pickering-Brown, Giacomina Rossi, Carlos Cruchaga, G. Binetti, Maria Landqvist Waldö, William W. Seeley, Jonathan D. Rohrer, Keith A. Josephs, Diego Albani, Wei Gu, Huei-Hsin Chiang, Luigi Ferrucci, H. Zhao, Howie Rosen, Pau Pastor, Alfredo Postiglione, Evelyn Jaros, Livia Bernardi, Dena G. Hernandez, Alberto Lleó, James B. Rowe, Parastoo Momeni, Maria Serpente, Huw R. Morris, Timothy D. Griffiths, Maria Grazia Spillantini, Alan J. Thomas, Maria Elena Conidi, M. Anfossi, Sabrina Pichler, Martine Vercelletto, Murray Grossman, Johannes C. M. Schlachetzki, Gianluigi Forloni, Dennis W. Dickson, Chiara Fenoglio, Olivier Piguet, John B.J. Kwok, Benedetta Nacmias, Harro Seelaar, Robert Perneczky, A. Baborie, Patrizia Rizzu, Y. Gao, Simon Mead, Janine Diehl-Schmid, Sara Ortega-Cubero, Mike A. Nalls, Daniela Galimberti, Annibale Alessandro Puca, Cristina Razquin, Mercè Boada, Johannes Attems, Luisa Benussi, Chiara Cupidi, Irene Piaceri, Xinghao Yu, Joseph E. Parisi, Alexander Kurz, John Collinge, James Uphill, Barbara Borroni, Francesca Frangipane, Caroline Graff, Bernd Ibach, D. M. A. Mann
Publikováno v:
Scientific reports, vol 10, iss 1
Scientific Reports, 10(1):12184. Nature Publishing Group
Scientific reports 10(1), 12184 (2020). doi:10.1038/s41598-020-68848-9
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, George-Hyslop, P S, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Cruts, M, Van Broeckhoven, C, Cappa, S F, Leber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebouvier, T, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P, Zhao, H, Zeng, P & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, Rowe, J B, Nielsen, J E, Hjermind, L E & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9
Scientific reports
Scientific Reports, 10(1):12184. Nature Publishing Group
Scientific reports 10(1), 12184 (2020). doi:10.1038/s41598-020-68848-9
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, McKeith, I G, Thomas, A J, Pietrini, P, Huey, E D, Wassermann, E M, Baborie, A, Jaros, E, Tierney, M C, Pastor, P, Razquin, C, Ortega-Cubero, S, Alonso, E, Perneczky, R, Diehl-Schmid, J, Alexopoulos, P, Kurz, A, Rainero, I, Rubino, E, Pinessi, L, Rogaeva, E, George-Hyslop, P S, Rossi, G, Tagliavini, F, Giaccone, G, Rowe, J B, Schlachetzki, J C M, Uphill, J, Collinge, J, Mead, S, Danek, A, Van Deerlin, V M, Grossman, M, Trojanowski, J Q, van der Zee, J, Cruts, M, Van Broeckhoven, C, Cappa, S F, Leber, I, Hannequin, D, Golfier, V, Vercelletto, M, Brice, A, Nacmias, B, Sorbi, S, Bagnoli, S, Piaceri, I, Nielsen, J E, Hjermind, L E, Riemenschneider, M, Mayhaus, M, Ibach, B, Gasparoni, G, Pichler, S, Gu, W, Rossor, M N, Fox, N C, Warren, J D, Spillantini, M G, Morris, H R, Rizzu, P, Heutink, P, Snowden, J S, Rollinson, S, Richardson, A, Gerhard, A, Bruni, A C, Maletta, R, Frangipane, F, Cupidi, C, Bernardi, L, Anfossi, M, Gallo, M, Conidi, M E, Smirne, N, Rademakers, R, Baker, M, Dickson, D W, Graff-Radford, N R, Petersen, R C, Knopman, D, Josephs, K A, Boeve, B F, Parisi, J E, Seeley, W W, Miller, B L, Karydas, A M, Rosen, H, van Swieten, J C, Dopper, E G P, Seelaar, H, Pijnenburg, Y A L, Scheltens, P, Logroscino, G, Capozzo, R, Novelli, V, Puca, A A, Franceschi, M, Postiglione, A, Milan, G, Sorrentino, P, Kristiansen, M, Chiang, H H, Graff, C, Pasquier, F, Rollin, A, Deramecourt, V, Lebouvier, T, Kapogiannis, D, Ferrucci, L, Pickering-Brown, S, Singleton, A B, Hardy, J, Momeni, P, Zhao, H, Zeng, P & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Gao, Y, Wang, T, Yu, X, Ferrari, R, Hernandez, D G, Nalls, M A, Rohrer, J D, Ramasamy, A, Kwok, J B J, Dobson-Stone, C, Brooks, W S, Schofield, P R, Halliday, G M, Hodges, J R, Piguet, O, Bartley, L, Thompson, E, Haan, E, Hernández, I, Ruiz, A, Boada, M, Borroni, B, Padovani, A, Cruchaga, C, Cairns, N J, Benussi, L, Binetti, G, Ghidoni, R, Forloni, G, Albani, D, Galimberti, D, Fenoglio, C, Serpente, M, Scarpini, E, Clarimón, J, Lleó, A, Blesa, R, Waldö, M L, Nilsson, K, Nilsson, C, Mackenzie, I R A, Hsiung, G Y R, Mann, D M A, Grafman, J, Morris, C M, Attems, J, Griffiths, T D, Rowe, J B, Nielsen, J E, Hjermind, L E & International FTD-Genomics Consortium (IFGC) 2020, ' Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis ', Scientific Reports, vol. 10, no. 1, 12184 . https://doi.org/10.1038/s41598-020-68848-9
Scientific reports
Funder: QingLan Research Project of Jiangsu for Outstanding Young Teachers
Funder: Project funded by Postdoctoral Science Foundation of Xuzhou Medical University
Funder: Priority Academic Program Development of Jiangsu Higher Education Inst
Funder: Project funded by Postdoctoral Science Foundation of Xuzhou Medical University
Funder: Priority Academic Program Development of Jiangsu Higher Education Inst
Autor:
Ole A. Andreassen, Vivianna M. Van Deerlin, David Simon, Claire E. Wegel, Guido Alves, Ruwani Wijeyekoon, Jodi Maple-Grødem, Alastair J. Noyce, Roger A. Barker, Bart P.C. van de Warrenburg, Peter Heutink, Shirley Eberly, J. Raphael Gibbs, Alexis Brice, Kumaraswamy Naidu Chitrala, Lasse Pihlstrøm, Marlies van Nimwegen, Khanh-Dung H. Nguyen, Ganqiang Liu, Bernard Ravina, Clemens R. Scherzer, Jean-Christophe Corvol, Bastiaan R. Bloem, Jacobus J. van Hilten, Karol Estrada, Faraz Faghri, Jonathan R. Evans, Daniel Weintraub, Ole-Bjørn Tysnes, Aaron G. Day-Williams, Hampton L. Leonard, Jonggeol J. Kim, Fabrice Danjou, David P. Breen, Samantha J. Hutten, Andrew B. Singleton, Hirotaka Iwaki, Peggy Auinger, Mike A. Nalls, Kirsten M. Scott, Dena G. Hernandez, Mathias Toft, Jacqueline Rick, Caroline H. Williams-Gray, Cornelis Blauwendraat
Publikováno v:
2019, ' Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts ', Movement Disorders, vol. 34, no. 12 . https://doi.org/10.1002/mds.27845
Movement Disorders, 34, 1839-1850
Movement disorders 34(12), 1839-1850 (2019). doi:10.1002/mds.27845
Mov Disord
Movement Disorders
Movement Disorders, 34, 12, pp. 1839-1850
Movement Disorders, 34, 1839-1850
Movement disorders 34(12), 1839-1850 (2019). doi:10.1002/mds.27845
Mov Disord
Movement Disorders
Movement Disorders, 34, 12, pp. 1839-1850
Item does not contain fulltext BACKGROUND: Several reports have identified different patterns of Parkinson's disease progression in individuals carrying missense variants in GBA or LRRK2 genes. The overall contribution of genetic factors to the sever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d75d743e4735219496720da03a92501
https://www.pure.ed.ac.uk/ws/files/112990604/Breen_GWAS_MovtDisorders.pdf
https://www.pure.ed.ac.uk/ws/files/112990604/Breen_GWAS_MovtDisorders.pdf
Autor:
Christine Klein, Eva-Juliane Vollstedt, Peter Heutink, Enza Maria Valente, Ai Huey Tan, Katja Lohmann, Niccolo E. Mencacci, Shen-Yang Lim, Micol Avenali, Kishore R. Kumar, Harutyun Madoev, Lara Lange
Publikováno v:
Journal of the Neurological Sciences. 429:118257
Autor:
Enza Maria Valente, Eva-Juliane Vollstedt, Christine Klein, Shen-Yang Lim, Kishore R. Kumar, Ai Huey Tan, Harutyun Madoev, Niccolo E. Mencacci, Peter Heutink, Micol Avenali, Katja Lohmann, Lara Lange
Publikováno v:
Journal of the Neurological Sciences. 429:118256
Autor:
Christian Deuschle, Peter Heutink, Carlo Wilke, Thomas Gasser, Frank Gillardon, Cornelis Blauwendraat, Markus A. Hobert, Matthis Synofzik, Iris E. Jansen, Florian G. Metzger, Walter Maetzler
Publikováno v:
Neurodegenerative Diseases. 17:83-88
Background and Objective: Reduced progranulin levels are a hallmark of frontotemporal dementia (FTD) caused by loss-of-function (LoF) mutations in the progranulin gene (GRN). However, alterations of central nervous progranulin expression also occur i
Autor:
Cristina Tejera-Parrado, Jean-christophe Corvol, Huw Morris, Rauan Kaiyrzhanov, Sebastian Schreglmann, Mie Rizig, Sara Bandrés Ciga, Francisco Javier Barrero Hernández, Patrick Lewis, Nicholas Wood, Claudia Schulte, John Quinn, Astrid Daniela Adarmes Gómez, Juan Carlos Martinez Castrillo, Berta María Pascual Sedano, Victoria Alvarez, Niccolò Emanuele Mencacci, Thomas Gasser, Ziv Gan-Or, Luis Bonet-Ponce, Adolfo Mínguez-Castellanos, Jose Bras, J. Raphael Gibbs, Monica Diez-Fairen, Viorica Chelban, Ruth Lovering, Jon Infante, Oriol Dols Icardo, Hirotaka Iwaki, Rita Guerreiro, John Hardy, Mario Ezquerra, Kin Ying Mok, Kerri J Kinghorn, Beatriz De la Casa-Fages, Peter Heutink, Manuel Menéndez González, Francisco Escamilla Sevilla, Sara Saez-Atienzar, Alexis Brice, Ignacio Alvarez, Pille Taba
Publikováno v:
Movement
Movement disorders : official journal of the Movement Disorder Society, vol 34, iss 4
Movement disorders : official journal of the Movement Disorder Society, vol 34, iss 4
Background PD is a complex polygenic disorder. In recent years, several genes from the endocytic membrane-trafficking pathway have been suggested to contribute to disease etiology. However, a systematic analysis of pathway-specific genetic risk facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc57b205c12177e309814c86ba6bcec
http://livrepository.liverpool.ac.uk/3031818/1/Bandres-Ciga_et_al-2019-Movement_Disorders.pdf
http://livrepository.liverpool.ac.uk/3031818/1/Bandres-Ciga_et_al-2019-Movement_Disorders.pdf