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Junker, Johanna and Lange, Lara M. and Vollstedt, Eva-Juliane and Roopnarain, Karisha and Doquenia, Maria Leila M. and Annuar, Azlina Ahmad and Avenali, Micol and Bardien, Soraya and Bahr, Natascha and Ellis, Melina and Galandra, Caterina and Gasser, Thomas and Heutink, Peter and Illarionova, Anastasia and Kanana, Yuliia and Sarmiento, Ignacio J. Keller and Kumar, Kishore R. and Lim, Shen-Yang and Madoev, Harutyun and Mata, Ignacio F. and Mencacci, Niccolo E. and Nalls, Mike A. and Padmanabhan, Shalini and Shambetova, Cholpon and Solle, J. C. and Tan, Ai-Huey and Trinh, Joanne and Valente, Enza Maria and Singleton, Andrew and Blauwendraat, Cornelis and Lohmann, Katja and Fang, Zih-Hua and Klein, Christine (2024) Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale. Movement Disorders, 39 (10). pp. 1868-1873. ISSN 0885-3185, DOI https://doi.org/10.1002/mds.29925.
Jagota, Priya and Ugawa, Yoshikazu and Aldaajani, Zakiyah and Ibrahim, Norlinah Mohamed and Ishiura, Hiroyuki and Nomura, Yoshiko and Tsuji, Shoji and Diesta, Cid and Hattori, Nobutaka and Onodera, Osamu and Bohlega, Saeed and Al-Din, Amir and Lim, Shen-Yang and Lee, Jee-Young and Jeon, Beomseok and Pal, Pramod Kumar and Shang, Huifang and Fujioka, Shinsuke and Kukkle, Prashanth Lingappa and Phokaewvarangkul, Onanong and Lin, Chin-Hsien and Shambetova, Cholpon and Bhidayasiri, Roongroj (2023) Nine hereditary movement disorders first described in Asia: their history and evolution. Journal of Movement Disorders, 16 (3). pp. 231-247. ISSN 2005-940X, DOI https://doi.org/10.14802/jmd.23065.
