HuGE Literature Finder
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| Glucocerebrosidase Activity is not Associated with Parkinson's Disease Risk or Severity. Movement disorders : official journal of the Movement Disorder Society 2021 Sep . Omer Nurit, Giladi Nir, Gurevich Tanya, Bar-Shira Anat, Gana-Weisz Mali, Glinka Tal, Goldstein Orly, Kestenbaum Meir, Cedarbaum Jesse M, Mabrouk Omar S, Fraser Kyle B, Shirvan Julia C, Orr-Urtreger Avi, Mirelman Anat, Thaler Avn |
| Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression. JAMA network open 2021 Apr 4 (4): e215845. Ortega Roberto A, Wang Cuiling, Raymond Deborah, Bryant Nicole, Scherzer Clemens R, Thaler Avner, Alcalay Roy N, West Andrew B, Mirelman Anat, Kuras Yuliya, Marder Karen S, Giladi Nir, Ozelius Laurie J, Bressman Susan B, Saunders-Pullman Rach |
| Sex effects on clinical features in LRRK2 G2385R carriers and non-carriers in Parkinson's disease. BMC neuroscience 2021 Mar 22 (1): 22. Cui Shi-Shuang, Fu Rao, Du Juan-Juan, Lin Yi-Qi, Huang Pei, Gao Chao, Zhou Hai-Yan, Chen Sheng- |
| Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients. Genetic testing and molecular biomarkers 2018 May . Chen Han, Yuan Lamei, Song Zhi, Deng Xiong, Yang Zhijian, Gong Lina, Zi Xiaohong, Deng H |
| PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2017 Jan . Noyce Alastair J, R'Bibo Lea, Peress Luisa, Bestwick Jonathan P, Adams-Carr Kerala L, Mencacci Niccolo E, Hawkes Christopher H, Masters Joseph M, Wood Nicholas, Hardy John, Giovannoni Gavin, Lees Andrew J, Schrag Anet |
| Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis. JAMA neurology 2015 Jan 72 (1): 58-65. Agalliu Ilir, San Luciano Marta, Mirelman Anat, Giladi Nir, Waro Bjorg, Aasly Jan, Inzelberg Rivka, Hassin-Baer Sharon, Friedman Eitan, Ruiz-Martinez Javier, Marti-Masso Jose Felix, Orr-Urtreger Avi, Bressman Susan, Saunders-Pullman Rach |
| Lrrk2 R1628P variant is a risk factor for essential tremor. Scientific reports 2015 5 9029. Chao Yin Xia, Ng Ebonne Yulin, Tan Louis, Prakash Kumar M, Au Wing-Lok, Zhao Yi, Tan Eng-Ki |
| Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers. Neurology 2011 Jul 77 (4): 325-33. Marras C, Schüle B, Schuele B, Munhoz R P, Rogaeva E, Langston J W, Kasten M, Meaney C, Klein C, Wadia P M, Lim S-Y, Chuang R S-I, Zadikof C, Steeves T, Prakash K M, de Bie R M A, Adeli G, Thomsen T, Johansen K K, Teive H A, Asante A, Reginold W, Lang A |
| Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease. Journal of the neurological sciences 2011 Jun . Giladi N, Mirelman A, Thaler A, Bar-Shira A, Gurevich T, Orr-Urtreger A |
| Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease. Archives of neurology 2009 Dec 66 (12): 1517-22. Alcalay Roy N, Mejia-Santana Helen, Tang Ming Xin, Rosado Llency, Verbitsky Miguel, Kisselev Sergey, Ross Barbara M, Louis Elan D, Comella Cynthia L, Colcher Amy, Jennings Danna, Nance Martha A, Bressman Susan, Scott William K, Tanner Caroline, Mickel Susan F, Andrews Howard F, Waters Cheryl H, Fahn Stanley, Cote Lucien J, Frucht Steven J, Ford Blair, Rezak Michael, Novak Kevin, Friedman Joseph H, Pfeiffer Ronald, Marsh Laura, Hiner Bradley, Siderowf Andrew, Caccappolo Elise, Ottman Ruth, Clark Lorraine N, Marder Karen |
| 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 |
| Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia. Parkinsonism & related disorders 2009 Feb 15 (2): 105-9. Mellick George D, Siebert Gerhard A, Funayama Manabu, Buchanan Daniel D, Li Yuanzhe, Imamichi Yoko, Yoshino Hiroyo, Silburn Peter A, Hattori Nobuta |
| 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 |
| 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 |
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- Page last updated:Jun 28, 2022
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