Human Genome Epidemiology Literature Finder
|
Records 1 - 16 (of 16 Records) |
| Query Trace: Neurodegenerative Diseases and LRRK2[original query] |
|---|
| Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations. Neurology 2008 Feb 70 (7): 521-7. Chen-Plotkin A S, Yuan W, Anderson C, McCarty Wood E, Hurtig H I, Clark C M, Miller B L, Lee V M-Y, Trojanowski J Q, Grossman M, Van Deerlin V |
| Analysis of the LRRK2 Gly2385Arg variant in primary dystonia and multiple system atrophy in Taiwan. Parkinsonism & related disorders 2008 14 (5): 393-6. Lu Chin-Song, Chang Hsiu-Chen, Weng Yi-Hsin, Chen Rou-Shayn, Bonifati Vincenzo, Wu-Chou Yah-Hu |
| 123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations. Journal of neurology 2011 1 258 (6): 1126-32. Valldeoriola Francesc, Gaig Carles, Muxí Africa, Navales Ignacio, Paredes Pilar, Lomeña Francisco, De la Cerda Andres, Buongiorno Mariateresa, Ezquerra Mario, Santacruz Pilar, Martí Maria Jose, Tolosa Eduar |
| Investigation of c9orf72 in 4 neurodegenerative disorders. Archives of neurology 2012 Dec 69 (12): 1583-90. Xi Zhengrui, Zinman Lorne, Grinberg Yakov, Moreno Danielle, Sato Christine, Bilbao Juan M, Ghani Mahdi, Hernández Isabel, Ruiz Agustín, Boada Mercè, Morón Francisco J, Lang Anthony E, Marras Connie, Bruni Amalia, Colao Rosanna, Maletta Raffaele G, Puccio Gianfranco, Rainero Innocenzo, Pinessi Lorenzo, Galimberti Daniela, Morrison Karen E, Moorby Catriona, Stockton Joanne D, Masellis Mario, Black Sandra E, Hazrati Lili-Naz, Liang Yan, van Haersma de With Jan, Fornazzari Luis, Villagra Roque, Rojas-Garcia Ricardo, Clarimón Jordi, Mayeux Richard, Robertson Janice, St George-Hyslop Peter, Rogaeva Ekateri |
| Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: a replication study in a Taiwanese cohort. Parkinsonism & related disorders 2012 Nov . Wu-Chou YH, Chen YT, Yeh TH, Chang HC, Weng YH, Lai SC, Huang CL, Chen RS, Huang YZ, Chen CC, Hung J, Chuang WL, Lin WY, Chen CH, Lu CS |
| Leucine-rich repeat kinase 2 modulates cyclooxygenase 2 and the inflammatory response in idiopathic and genetic Parkinson's disease. Neurobiology of aging 2014 May 35 (5): 1116-24. Lopez de Maturana Rakel, Aguila Julio C, Sousa Amaya, Vazquez Nerea, Del Rio Patricia, Aiastui Ana, Gorostidi Ana, Lopez de Munain Adolfo, Sanchez-Pernaute Rosar |
| Heterogeneity among patients with Parkinson's disease: cluster analysis and genetic association. Journal of the neurological sciences 2015 Apr 351 (1-2): 41-5. Ma Ling-Yan, Chan Piu, Gu Zhu-Qin, Li Fang-Fei, Feng T |
| MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
| A human microglia-like cellular model for assessing the effects of neurodegenerative disease gene variants. Science translational medicine 2017 12 9 (421): . Ryan Katie J, White Charles C, Patel Kruti, Xu Jishu, Olah Marta, Replogle Joseph M, Frangieh Michael, Cimpean Maria, Winn Phoebe, McHenry Allison, Kaskow Belinda J, Chan Gail, Cuerdon Nicole, Bennett David A, Boyd Justin D, Imitola Jaime, Elyaman Wassim, De Jager Philip L, Bradshaw Elizabeth |
| Analysis of 50 Neurodegenerative Genes in Clinically Diagnosed Early-Onset Alzheimer's Disease. International journal of molecular sciences 2019 Mar 20 (6): . Giau Vo Van, Senanarong Vorapun, Bagyinszky Eva, An Seong Soo A, Kim SangY |
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Movement disorders : official journal of the Movement Disorder Society 2019 12 34 (12): 1851-1863. Bandres-Ciga Sara, Ahmed Sarah, Sabir Marya S, Blauwendraat Cornelis, Adarmes-Gómez Astrid D, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Buiza-Rueda Dolores, Carrillo Fátima, Carrión-Claro Mario, Gómez-Garre Pilar, Jesús Silvia, Labrador-Espinosa Miguel A, Macias Daniel, Méndez-Del-Barrio Carlota, Periñán-Tocino Teresa, Tejera-Parrado Cristina, Vargas-González Laura, Diez-Fairen Monica, Alvarez Ignacio, Tartari Juan Pablo, Buongiorno Mariateresa, Aguilar Miquel, Gorostidi Ana, Bergareche Jesús Alberto, Mondragon Elisabet, Vinagre-Aragon Ana, Croitoru Ioana, Ruiz-Martínez Javier, Dols-Icardo Oriol, Kulisevsky Jaime, Marín-Lahoz Juan, Pagonabarraga Javier, Pascual-Sedano Berta, Ezquerra Mario, Cámara Ana, Compta Yaroslau, Fernández Manel, Fernández-Santiago Rubén, Muñoz Esteban, Tolosa Eduard, Valldeoriola Francesc, Gonzalez-Aramburu Isabel, Sanchez Rodriguez Antonio, Sierra María, Menéndez-González Manuel, Blazquez Marta, Garcia Ciara, Suarez-San Martin Esther, García-Ruiz Pedro, Martínez-Castrillo Juan Carlos, Vela-Desojo Lydia, Ruz Clara, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Mínguez-Castellanos Adolfo, Cerdan Debora, Tabernero Cesar, Gomez Heredia Maria Jose, Perez Errazquin Francisco, Romero-Acebal Manolo, Feliz Cici, Lopez-Sendon Jose Luis, Mata Marina, Martínez Torres Irene, Kim Jonggeol Jeffrey, Dalgard Clifton L, , Brooks Janet, Saez-Atienzar Sara, Gibbs J Raphael, Jorda Rafael, Botia Juan A, Bonet-Ponce Luis, Morrison Karen E, Clarke Carl, Tan Manuela, Morris Huw, Edsall Connor, Hernandez Dena, Simon-Sanchez Javier, Nalls Mike A, Scholz Sonja W, Jimenez-Escrig Adriano, Duarte Jacinto, Vives Francisco, Duran Raquel, Hoenicka Janet, Alvarez Victoria, Infante Jon, Marti Maria José, Clarimón Jordi, López de Munain Adolfo, Pastor Pau, Mir Pablo, Singleton Andrew, |
| Identification of susceptibility loci for cognitive impairment in a cohort of Han Chinese patients with Parkinson's disease. Neuroscience letters 2020 May 135034. Liu Hong-Jun, Li Xiao-Yan, Chen Hui, Yu Hui-Li, Tao Qing-Qing, Wu Zhi-Yi |
| A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia. Case reports in genetics 2020 2020 8813344. Smaili Imane, Hajjaj Imane, Razine Rachid, Tibar Houyam, Salmi Ayyoub, Bouslam Naima, Moussa Ahmed, Regragui Wafa, Bouhouche Ahm |
| Interactive Association Between Intronic Polymorphism (rs10506151) of the LRRK2 Gene and Type 2 Diabetes on Neurodegenerative Diseases. Pharmacogenomics and personalized medicine 2021 14 839-847. Huang Mei-Hsuen, Liu Yu-Fan, Nfor Oswald Ndi, Hsu Shu-Yi, Lin Wei-Yong, Chang Yuan-Shiun, Liaw Yung- |
| Early-Onset Parkinson Disease Screening in Patients From Nigeria. Frontiers in neurology 2021 2 11 594927. Milanowski Lukasz M, Oshinaike Olajumoke, Broadway Benjamin J, Lindemann Jennifer A, Soto-Beasley Alexandra I, Walton Ronald L, Hanna Al-Shaikh Rana, Strongosky Audrey J, Fiesel Fabienne C, Ross Owen A, Springer Wolfdieter, Ogun Shamsideen Abayomi, Wszolek Zbigniew |
| Genetic Screening of Patients with Sporadic Alzheimer's Disease and Frontotemporal Lobar Degeneration in the Chinese Population. Journal of Alzheimer's disease : JAD 2024 5 . Yaoru Li, Ziying Yang, Yanxin Zhang, Fang Liu, Jing Xu, Yaping Meng, Gebeili Xing, Xuqin Ruan, Jun Sun, Nan Zha |
- Page last reviewed:Feb 1, 2024
- Content source: