Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Neurologie [D14] [Sciences de la santé humaine]"'
Autor:
Sugier, Pierre-Emmanuel, Lucotte, Elise A., Domenighetti, Cloé, Law, Matthew H., Iles, Mark M., Brown, Kevin, Amos, Christopher, McKay, James D., Hung, Rayjean J., Karimi, Mojgan, Bacq-Daian, Delphine, Boland-Augé, Anne, Olaso, Robert, Deleuze, Jean-François, Lesueur, Fabienne, Ostroumova, Evgenia, Kesminiene, Ausrele, de Vathaire, Florent, Guénel, Pascal, consortium, The Epithyr, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj Reddy, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Singleton, Andrew B., Hernandez, Dena G., Edsall, Connor, Mellick, George D., Zimprich, Alexander, Pirker, Walter, Rogaeva, Ekaterina, Lang, Anthony E., Koks, Sulev, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugénie, Brockmann, Kathrin, Deutschländer, Angela B., Hadjigeorgiou, Georges M., Dardiotis, Efthimios, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, van de Warrenburg, Bart P. C., Bloem, Bastiaan R., Aasly, Jan, Toft, Mathias, Pihlstrøm, Lasse, Guedes, Leonor Correia, Ferreira, Joaquim J., Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy, Ran, Caroline, Belin, Andrea C., Puschmann, Andreas, Rödström, Emil Ygland, Clarke, Carl E., Morrison, Karen E., Tan, Manuela, Krainc, Dimitri, Burbulla, Lena F., Farrer, Matt J., Krüger, Rejko, Gasser, Thomas, Sharma, Manu, Landoulsi, Zied, consortium, Courage-PD, Truong, Thérèse, Elbaz, Ales
Publikováno v:
Movement Disorders, 38, 4, pp. 604-615
the EPITHYR consortium, the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) consortium, Sugier, PE, Lucotte, E A, Domenighetti, C, Law, M H, Iles, M M, Brown, K, Amos, C, McKay, J D, Hung, R J, Karimi, M, Bacq-Daian, D, Boland-Augé, A, Olaso, R, Deleuze, J, Lesueur, F, Ostroumova, E, Kesminiene, A, de Vathaire, F, Guénel, P, Sreelatha, A A K, Schulte, C, Grover, S, May, P, Bobbili, D R, Radivojkov-Blagojevic, M, Lichtner, P, Singleton, A B, Hernandez, D G, Edsall, C, Mellick, G D, Zimprich, A, Pirker, W, Rogaeva, E, Lang, A E, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, JC, Chartier-Harlin, MC, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S & Morrison, K E 2023, ' Investigation of shared genetic risk factors between Parkinson's disease and cancers ', Movement Disorders . https://doi.org/10.1002/mds.29337
Movement disorders 38(4), 604-615 (2023). doi:10.1002/mds.29337
the EPITHYR consortium, the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) consortium, Sugier, PE, Lucotte, E A, Domenighetti, C, Law, M H, Iles, M M, Brown, K, Amos, C, McKay, J D, Hung, R J, Karimi, M, Bacq-Daian, D, Boland-Augé, A, Olaso, R, Deleuze, J, Lesueur, F, Ostroumova, E, Kesminiene, A, de Vathaire, F, Guénel, P, Sreelatha, A A K, Schulte, C, Grover, S, May, P, Bobbili, D R, Radivojkov-Blagojevic, M, Lichtner, P, Singleton, A B, Hernandez, D G, Edsall, C, Mellick, G D, Zimprich, A, Pirker, W, Rogaeva, E, Lang, A E, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, JC, Chartier-Harlin, MC, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S & Morrison, K E 2023, ' Investigation of shared genetic risk factors between Parkinson's disease and cancers ', Movement Disorders . https://doi.org/10.1002/mds.29337
Movement disorders 38(4), 604-615 (2023). doi:10.1002/mds.29337
BackgroundEpidemiological studies that examined the association between Parkinson's disease (PD) and cancers led to inconsistent results, but they face a number of methodological difficulties.ObjectiveWe used results from genome-wide association stud
Autor:
Anouk F. J. Geraets, Anja K. Leist, Kay Deckers, Frans R. J. Verhey, Miranda T. Schram, Sebastian Köhler
Publikováno v:
Psychological Medicine. Cambridge University Press
info:eu-repo/grantAgreement/EC/H2020/803239
info:eu-repo/grantAgreement/EC/H2020/803239
Background Individuals with depression have an increased dementia risk, which might be due to modifiable risk factors for dementia. This study investigated the extent to which the increased risk for dementia in depression is explained by modifiable d
Autor:
Agnes Langer, Lara Lucke-Paulig, Lucia Gassner, Rejko Krüger, Daniel Weiss, Alireza Gharabaghi, Heidemarie Zach, Walter Maetzler, Markus A. Hobert
Publikováno v:
Neuromodulation: Technology at the Neural Interface. 26:364-373
INTRODUCTION: Patients with advanced Parkinson disease (PD) often experience problems with mobility, including walking under single- (ST) and dual-tasking (DT) conditions. The effects of deep brain stimulation in the subthalamic nucleus (DBS) versus
Autor:
Sumaiya Iqbal, Tobias Brünger, Eduardo Pérez-Palma, Marie Macnee, Andreas Brunklaus, Mark J Daly, Arthur J Campbell, David Hoksza, Patrick May, Dennis Lal
Publikováno v:
Brain. 146:519-533
Neurodevelopmental disorders (NDDs), including severe paediatric epilepsy, autism and intellectual disabilities are heterogeneous conditions in which clinical genetic testing can often identify a pathogenic variant. For many of them, genetic therapie
Autor:
Anouk F. J. Geraets, Sebastian Köhler, Laura WM Vergoossen, Walter H. Backes, Coen D.A. Stehouwer, Frans RJ Verhey, Jacobus FA Jansen, Thomas T. van Sloten, Miranda T. Schram
Publikováno v:
Psychological Medicine, 1-11. Cambridge University Press
STARTPAGE=1;ENDPAGE=11;ISSN=0033-2917;TITLE=Psychological Medicine
STARTPAGE=1;ENDPAGE=11;ISSN=0033-2917;TITLE=Psychological Medicine
Background Altered white matter brain connectivity has been linked to depression. The aim of this study was to investigate the association of markers of white matter connectivity with prevalence, incidence and course of depressive symptoms. Methods M
Autor:
Anne-Marie Hanff, Christopher McCrum, Armin Rauschenberger, Gloria A. Aguayo, Maurice P. Zeegers, Anja K. Leist, Rejko Krüger
Publikováno v:
Parkinsonism & Related Disorders, 112:105442. ELSEVIER SCI LTD
Introduction: Functional mobility is an important outcome for people with Parkinson's disease (PwP). Despite this, there is no established patient-reported outcome measure that serves as a gold standard for assessing patient-reported functional mobil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c39af6cfd55c070f46f3dc7586b6604
https://cris.maastrichtuniversity.nl/en/publications/cd38c386-efe5-49dd-a479-d369b950664d
https://cris.maastrichtuniversity.nl/en/publications/cd38c386-efe5-49dd-a479-d369b950664d
Autor:
Arena, Giuseppe, Landoulsi, Zied, Grossmann, Dajana, Vitali, Armelle, Delcambre, Sylvie, Baron, Alexandre, Antony, Paul, Boussaad, Ibrahim, Bobbili, Dheeraj Reddy, Sreelatha, Ashwin Ashok Kumar, Pavelka, Lukas, Klein, Christine, Seibler, Philip, Glaab, Enrico, Sharma, Manu, Krüger, Rejko, May, Patrick, Grünewald, Anne
Publikováno v:
info:eu-repo/grantAgreement/EC/H2020/779282
Background Parkinson's disease (PD) is the fastest growing neurodegenerative disorder, with affected individuals expected to double during the next 20 years. This raises the urgent need to better understand the genetic architecture and downstream cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2658::307586821edb8bb81114f954b98ce48e
http://orbilu.uni.lu/handle/10993/55367
http://orbilu.uni.lu/handle/10993/55367
Autor:
Peiris, Sinthuja, Landoulsi, Zied, Pavelka, Lukas, Schulte, Claudia, Buena-Atienza, Elena, Gross, Caspar, Hauser, Ann-Kathrin, Bobbili, Dheeraj Reddy, Casadei, Nicolas, May, Patrick, Krüger, Rejko, Consortium, The NCER-PD
Heterozygous variants in the glucocerebrosidase GBA gene are an increasingly recognized risk factor for Parkinson's disease (PD). Due to the pseudogene GBAP1 that shares 96\% sequence homology with the GBA coding region, accurate variant calling by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2658::3a1326ce432d2c452bb3b8130f07762d
http://orbilu.uni.lu/handle/10993/55244
http://orbilu.uni.lu/handle/10993/55244
Autor:
Günter Höglinger, Claudia Schulte, Wolfgang H. Jost, Alexander Storch, Dirk Woitalla, Rejko Krüger, Björn Falkenburger, Kathrin Brockmann
Publikováno v:
Journal of neural transmission 129(9), 1219-1233 (2022). doi:10.1007/s00702-022-02511-7
Given the clear role of GBA in the pathogenesis of Parkinson’s disease (PD) and its impact on phenotypical characteristics, this review provides an overview of the current knowledge of GBA-associated PD with a special focus on clinical trajectories
Autor:
Vollstedt, Eva-Juliane, Schaake, Susen, Lohmann, Katja, Padmanabhan, Shalini, Brice, Alexis, Lesage, Suzanne, Tesson, Christelle, Vidailhet, Marie, Wurster, Isabel, Hentati, Faycel, Mirelman, Anat, Giladi, Nir, Karen, Marder, Waters, Cheryl, Fahn, Stanley, Kasten, Meike, Brüggemann, Norbert, Borsche, Max, Foroud, Tatiana, Tolosa, Eduardo, Garrido, Alicia, Annesi, Grazia, Gagliardi, Monica, Bozi, Maria, Stefanis, Leonidas, Ferreira, Joaquim J., Correia Guedes, Leonor, Avenali, Micol, Petrucci, Simona, Clark, Lorraine, Fedotova, Ekaterina Y., Abramycheva, Natalya Y., Alvarez, Victoria, Menéndez-González, Manuel, Jesús Maestre, Silvia, Gómez-Garre, Pilar, Mir, Pablo, Belin, Andrea Carmine, Ran, Caroline, Lin, Chin-Hsien, Kuo, Ming-Che, Crosiers, David, Wszolek, Zbigniew K., Ross, Owen A., Jankovic, Joseph, Nishioka, Kenya, Funayama, Manabu, Clarimon, Jordi, Williams-Gray, Caroline H., Camacho, Marta, Cornejo-Olivas, Mario, Torres-Ramirez, Luis, Wu, Yih-Ru, Lee-Chen, Guey-Jen, Morgadinho, Ana, Pulkes, Teeratorn, Termsarasab, Pichet, Berg, Daniela, Gregor, Kuhlenbäumer, Kühn, Andrea A., Borngräber, Friederike, de Michele, Giuseppe, De Rosa, Anna, Zimprich, Alexander, Puschmann, Andreas, Mellick, George D., Jolanta, Dorszewska, Carr, Jonathan, Ferese, Rosangela, Stefano, Gambardella, Chase, Bruce, Markopoulou, Katerina, Wataru, Satake, Toda, Tatsushi, Rossi, Malco, Merello, Marcelo, Lynch, Timothy, Olszewska, Diana A., Lim, Shen-Yang, Ahmad-Annuar, Azlina, Tan, Ai Huey, Al-Mubarak, Bashayer, Hanagasi, Hasmet, Koziorowski, Dariusz, Ertan, Sibel, Gen c, Gen Cer, de Carvalho Aguiar, Patricia, Barkhuizen, Melinda, Pimentel, Marcia M. G., Saunders-Pullman, Rachel, van de Warrenburg, Bart, Bressman, Susan, Toft, Mathias, Appel-Cresswell, Silke, Lang, Anthony E., Skorvanek, Matej, Boon, Agnita J. W., Krüger, Rejko, Sammler, Esther M., Tumas, Vitor, Zhang, Bao-Rong, Garraux, Gaetan, Chung, Sun Ju, Joong, Kim Yun, Winkelmann, Juliane, Sue, Carolyn M., Eng-King, Tan, Damásio, Joana, Klivényi, Péter, Kostic, Vladimir S., Arkadir, David, Martikainen, Mika, Borges, Vanderci, Hertz, Jens Michael, Brighina, Laura, Spitz, Mariana, Suchowersky, Oksana, Riess, Olaf, Parimal, Das, Mollenhauer, Brit, Gatto, Emilia M., Skaalum, Petersen Maria, Wu, Ruey-Meei, Illarioshkin, Sergey N., Valente, Enza Maria, Aasly, Jan O., Aasly, Anna, N, Alcalay Roy, Thaler, Avner, Farrer, Matthew J., Kathrin, Brockmann, Corvol, Jean-Christophe, Klein, Christine, Albanese, Alberto, Alcalay, Roy N., Aldakheel, Amaal, Alkhairallah, Thamer, Bashayer, Al-Mubarak, Al-Tassan, Nada, Paolo, Amami, Araujo, Leite Marco Antonio, Ferraz, Henrique Ballalai, Bardien, Soraya, Melinda, Barkhuizen, Barrett, Matthew J., Ba sak, A. Nazl I, Bilgic, Basar, Bloem, Bastiaan R., Bonifati, Vincenzo, Brockmann, Kathrin, Cesarini, Martin Emiliano, Ju, Chung Sun, Guedes, Leonor Correia, Lorraine, Clark, Dieguez, Elena, Dorszewska, Jolanta, Fung, Victor S. C., Pilar, Gómez-Garre, Hattori, Nobutaka, Faycel, Hentati, Januario, Cristina, Maestre, Silvia Jesús, Kaasinen, Valtteri, Hiroshi, Kataoka, Kievit, Anneke A., Kim, Yun Joong, Christine, Klein, Kuhlenbäumer, Gregor, Lim, Jia Lun, Timothy, Lynch, Marder, Karen, May, Patrick, McCarthy, Allan, Briceno, Hugo Morales, Morris, Huw, Mosejova, Alexandra, Cakmak, Özgür Öztop, Orr-Urtreger, Avi, Pachchek, Sinthuja, Periñ\'an, Maria Teresa, Procopio, Radha, Ruiz-Martinez, Javier, Pereira, João Santos, Satake, Wataru, Soto-Beasley, Alexandra I., Sousa, Mário, Tan, Eng-King, Tepge c, Fatih, Uyguner, Oya, Walton, Ronald L., H, Williams-Gray Caroline, Isabel, Wurster, Bao-Rong, Zhang
Publikováno v:
info:eu-repo/grantAgreement/EC/H2020/645360
BACKGROUND: As gene-targeted therapies are increasingly being developed for Parkinson's disease (PD), identifying and characterizing carriers of specific genetic pathogenic variants is imperative. Only a small fraction of the estimated number of subj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2658::0bf8d876dcc8574ecffaf40374e28a0d
http://orbilu.uni.lu/handle/10993/55245
http://orbilu.uni.lu/handle/10993/55245