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  4. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
 
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Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

Journal
Movement disorders : official journal of the Movement Disorder Society
Journal Volume
38
Journal Issue
2
Pages
286
Date Issued
2023-02-01
Author(s)
Vollstedt, Eva-Juliane
Schaake, Susen
Lohmann, Katja
Padmanabhan, Shalini
Brice, Alexis
Lesage, Suzanne
Tesson, Christelle
Vidailhet, Marie
Wurster, Isabel
Hentati, Faycel
Mirelman, Anat
Alvarez, Victoria
Menéndez-González, Manuel
Jesús Maestre, Silvia
Gómez-Garre, Pilar
Mir, Pablo
Belin, Andrea Carmine
Ran, Caroline
CHIN-HSIEN LIN  
MING-CHE KUO  
Crosiers, David
Dorszewska, Jolanta
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
Carr, Jonathan
Wu, Yih-Ru
Lee-Chen, Guey-Jen
Morgadinho, Ana
Pulkes, Teeratorn
Termsarasab, Pichet
Berg, Daniela
Kuhlenbäumer, Gregor
Kühn, Andrea A
Borngräber, Friederike
de Michele, Giuseppe
Ferese, Rosangela
De Rosa, Anna
Zimprich, Alexander
Puschmann, Andreas
Mellick, George D
Gambardella, Stefano
Chase, Bruce
Markopoulou, Katerina
Satake, Wataru
Toda, Tatsushi
Rossi, Malco
Merello, Marcelo
Zhang, Bao-Rong
Lynch, Timothy
Olszewska, Diana A
Lim, Shen-Yang
Ahmad-Annuar, Azlina
Tan, Ai Huey
Al-Mubarak, Bashayer
Hanagasi, Hasmet
Koziorowski, Dariusz
Ertan, Sibel
Genç, Gençer
Garraux, Gaetan
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
Chung, Sun Ju
Boon, Agnita J W
Krüger, Rejko
Sammler, Esther M
Tumas, Vitor
Kim, Yun Joong
Winkelmann, Juliane
Sue, Carolyn M
Tan, Eng-King
Damásio, Joana
Klivényi, Péter
Kostic, Vladimir S
Giladi, Nir
Arkadir, David
Martikainen, Mika
Borges, Vanderci
Hertz, Jens Michael
Brighina, Laura
Spitz, Mariana
Suchowersky, Oksana
Riess, Olaf
Das, Parimal
Mollenhauer, Brit
Marder, Karen
Gatto, Emilia M
Petersen, Maria Skaalum
Hattori, Nobutaka
RUEY-MEEI WU  
Illarioshkin, Sergey N
Valente, Enza Maria
Aasly, Jan O
Aasly, Anna
Alcalay, Roy N
Thaler, Avner
Waters, Cheryl
Farrer, Matthew J
Brockmann, Kathrin
Corvol, Jean-Christophe
Klein, Christine
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
DOI
10.1002/mds.29288
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/632652
URL
https://api.elsevier.com/content/abstract/scopus_id/85147202939
Abstract
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 subjects with monogenic PD worldwide are currently represented in the literature and availability of clinical data and clinical trial-ready cohorts is limited.
Subjects
Parkinson's disease; monogenic PD
SDGs

[SDGs]SDG3

[SDGs]SDG17

Publisher
WILEY
Type
journal article

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