HuGE Literature Finder
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| 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 |
| Brain and Cerebrospinal Fluid ?-Synuclein Real-Time Quaking-Induced Conversion Identifies Lewy Body Pathology in LRRK2-PD. Movement disorders : official journal of the Movement Disorder Society 2022 12 . Garrido Alicia, Fairfoul Graham, Tolosa Eduardo, Marti Maria J, Ezquerra Mario, Green Alison J |
| Elevated Urinary Rab10 Phosphorylation in Idiopathic Parkinson Disease. Movement disorders : official journal of the Movement Disorder Society 2022 5 37 (7): 1454-1464. Wang Shijie, Unnithan Shakthi, Bryant Nicole, Chang Allison, Rosenthal Liana S, Pantelyat Alexander, Dawson Ted M, Al-Khalidi Hussein R, West Andrew |
| Serum MicroRNAs Predict Isolated Rapid Eye Movement Sleep Behavior Disorder and Lewy Body Diseases. Movement disorders : official journal of the Movement Disorder Society 2022 8 37 (10): 2086-2098. Soto Marta, Iranzo Alex, Lahoz Sara, Fernández Manel, Serradell Mónica, Gaig Carles, Melón Paula, Martí Maria-Jose, Santamaría Joan, Camps Jordi, Fernández-Santiago Rubén, Ezquerra Mar |
| Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk. Movement disorders : official journal of the Movement Disorder Society 2021 Sep . Lake Julie, Reed Xylena, Langston Rebekah G, Nalls Mike A, Gan-Or Ziv, Cookson Mark R, Singleton Andrew B, Blauwendraat Cornelis, Leonard Hampton L, |
| 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- |
| Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Movement disorders : official journal of the Movement Disorder Society 2021 5 36 (8): 1795-1804. Iwaki Hirotaka, Leonard Hampton L, Makarious Mary B, Bookman Matt, Landin Barry, Vismer David, Casey Bradford, Gibbs J Raphael, Hernandez Dena G, Blauwendraat Cornelis, Vitale Daniel, Song Yeajin, Kumar Dinesh, Dalgard Clifton L, Sadeghi Mahdiar, Dong Xianjun, Misquitta Leonie, Scholz Sonja W, Scherzer Clemens R, Nalls Mike A, Biswas Shameek, Singleton Andrew B, , , |
| Age at Onset of LRRK2 p.Gly2019Ser Is Related to Environmental and Lifestyle Factors. Movement disorders : official journal of the Movement Disorder Society 2020 9 35 (10): 1854-1858. Lüth Theresa, König Inke R, Grünewald Anne, Kasten Meike, Klein Christine, Hentati Faycel, Farrer Matthew, Trinh Joan |
| Clinical and Dopamine Transporter Imaging Characteristics of Leucine Rich Repeat Kinase 2 (LRRK2) and Glucosylceramidase Beta (GBA) Parkinson's Disease Participants in the Parkinson's Progression Markers Initiative: A Cross-Sectional Study. Movement disorders : official journal of the Movement Disorder Society 2020 2 35 (5): 833-844. Simuni Tanya, Brumm Michael C, Uribe Liz, Caspell-Garcia Chelsea, Coffey Christopher S, Siderowf Andrew, Alcalay Roy N, Trojanowski John Q, Shaw Leslie M, Seibyl John, Singleton Andrew, Toga Arthur W, Galasko Doug, Foroud Tatiana, Nudelman Kelly, Tosun-Turgut Duygu, Poston Kathleen, Weintraub Daniel, Mollenhauer Brit, Tanner Caroline M, Kieburtz Karl, Chahine Lana M, Reimer Alyssa, Hutten Samantha, Bressman Susan, Marek Kenneth, |
| Screening Gene Mutations in Chinese Patients With Benign Essential Blepharospasm. Frontiers in neurology 2020 2 10 1387. Dong Hongjuan, Luo Ying, Fan Shanghua, Yin Bo, Weng Chao, Peng B |
| A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement disorders : official journal of the Movement Disorder Society 2019 2 34 (4): 506-515. Lin Chin-Hsien, Chen Pei-Lung, Tai Chun-Hwei, Lin Hang-I, Chen Chih-Shan, Chen Meng-Ling, Wu Ruey-Me |
| Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study. The Lancet. Neurology 2019 11 19 (1): 71-80. Simuni Tanya, Uribe Liz, Cho Hyunkeun Ryan, Caspell-Garcia Chelsea, Coffey Christopher S, Siderowf Andrew, Trojanowski John Q, Shaw Leslie M, Seibyl John, Singleton Andrew, Toga Arthur W, Galasko Doug, Foroud Tatiana, Tosun Duygu, Poston Kathleen, Weintraub Daniel, Mollenhauer Brit, Tanner Caroline M, Kieburtz Karl, Chahine Lana M, Reimer Alyssa, Hutten Samantha J, Bressman Susan, Marek Kenneth, |
| Higher Urine bis(Monoacylglycerol)Phosphate Levels in LRRK2 G2019S Mutation Carriers: Implications for Therapeutic Development. Movement disorders : official journal of the Movement Disorder Society 2019 9 35 (1): 134-141. Alcalay Roy N, Hsieh Frank, Tengstrand Elizabeth, Padmanabhan Shalini, Baptista Marco, Kehoe Caitlin, Narayan Sushma, Boehme Amelia K, Merchant Kalpa |
| 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:Mar 22, 2023
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