Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Movement Disorders and SNCA[original query] |
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Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. Neurogenetics 2008 Oct 9 (4): 263-9. Choi Jung Mi, Woo Myoung Soo, Ma Hyeo-Il, Kang Suk Yun, Sung Young-Hee, Yong Seok Woo, Chung Sun Ju, Kim Joong-Seok, Shin Hae-won, Lyoo Chul Hyoung, Lee Phil Hyu, Baik Jong Sam, Kim Sang-Jin, Park Mee Young, Sohn Young Ho, Kim Jin-Ho, Kim Jae Woo, Lee Myung Sik, Lee Myoung Chong, Kim Dong-Hyun, Kim Yun Joo |
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations. Movement disorders : official journal of the Movement Disorder Society 2009 Apr 24 (5): 662-6. Camargos Sarah Teixeira, Dornas Leonardo Oliveira, Momeni Parastoo, Lees Andrew, Hardy John, Singleton Andrew, Cardoso Francis |
Parafoveal thinning of inner retina is associated with visual dysfunction in Lewy body diseases. Movement disorders : official journal of the Movement Disorder Society 2019 5 34 (9): 1315-1324. Murueta-Goyena Ane, Del Pino Rocío, Reyero Paula, Galdós Marta, Arana Begoña, Lucas-Jiménez Olaia, Acera Marian, Tijero Beatriz, Ibarretxe-Bilbao Naroa, Ojeda Natalia, Peña Javier, Cortés Jesús, Gómez-Esteban Juan Carlos, Gabilondo Iñi |
Metal Exposure and SNCA rs356219 Polymorphism Associated With Parkinson Disease and Parkinsonism. Frontiers in neurology 2020 12 11 556337. Lucchini Roberto G, Guazzetti Stefano, Renzetti Stefano, Broberg Karin, Caci Margherita, Covolo Loredana, Crippa Patrizia, Gelatti Umberto, Hashim Dana, Oppini Manuela, Pepe Fulvio, Pilotto Andrea, Passeri Chiara, Placidi Donatella, Rizzetti Maira Cristina, Turla Marinella, Wahlberg Karin, Padovani Alessand |
A Novel SNCA A30G Mutation Causes Familial Parkinson's Disease. Movement disorders : official journal of the Movement Disorder Society 2021 2 36 (7): 1624-1633. Liu Hui, Koros Christos, Strohäker Timo, Schulte Claudia, Bozi Maria, Varvaresos Stefanos, Ibáñez de Opakua Alain, Simitsi Athina Maria, Bougea Anastasia, Voumvourakis Konstantinos, Maniati Matina, Papageorgiou Sokratis G, Hauser Ann-Kathrin, Becker Stefan, Zweckstetter Markus, Stefanis Leonidas, Gasser Thom |
GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based Study. Movement disorders : official journal of the Movement Disorder Society 2022 2 37 (5): 1016-1027. Szwedo Aleksandra A, Dalen Ingvild, Pedersen Kenn Freddy, Camacho Marta, Bäckström David, Forsgren Lars, Tzoulis Charalampos, Winder-Rhodes Sophie, Hudson Gavin, Liu Ganqiang, Scherzer Clemens R, Lawson Rachael A, Yarnall Alison J, Williams-Gray Caroline H, Macleod Angus D, Counsell Carl E, Tysnes Ole-Bjørn, Alves Guido, Maple-Grødem Jodi, |
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China. NPJ Parkinson's disease 2023 5 9 (1): 76. Yi-Min Sun, Xin-Yue Zhou, Xiao-Niu Liang, Jin-Ran Lin, Yi-Dan Xu, Chen Chen, Si-Di Wei, Qi-Si Chen, Feng-Tao Liu, Jue Zhao, Yi-Lin Tang, Bo Shen, Lin-Hua Gan, Boxun Lu, Zheng-Tong Ding, Yu An, Jian-Jun Wu, Jian Wa |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Jun 11, 2024
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