Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Tremor and LRRK2[original query] |
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| The LRRK2 I2012T, G2019S and I2020T mutations are not common in patients with essential tremor. Neuroscience letters 2006 Oct 407 (2): 97-100. Deng Hao, Le WeiDong, Davidson Anthony L, Xie WenJie, Jankovic Jose |
| LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance. Archives of neurology 2006 Mar 63 (3): 377-82. Gaig Carles, Ezquerra Mario, Marti Maria Jose, Muñoz Esteban, Valldeoriola Francesc, Tolosa Eduar |
| A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC neurology 2006 6 (): 47. Fung HC, Chen CM, Hardy J, Singleton AB, Wu YR |
| Genetic analysis of LRRK2 P755L variant in Caucasian patients with Parkinson's disease. Neuroscience letters 2007 May 419 (2): 104-7. Deng Hao, Le Weidong, Huang Maosheng, Xie Wenjie, Pan Tianghong, Jankovic Jose |
| Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2007 May 22 (7): 982-9. Huang Yue, Halliday Glenda M, Vandebona Himesha, Mellick George D, Mastaglia Frank, Stevens Julia, Kwok John, Garlepp Michael, Silburn Peter A, Horne Malcolm K, Kotschet Katya, Venn Alison, Rowe Dominic B, Rubio Justin P, Sue Carolyn |
| LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. The Lancet. Neurology 2008 Jul 7 (7): 591-4. Hulihan Mary M, Ishihara-Paul Lianna, Kachergus Jennifer, Warren Liling, Amouri Rim, Elango Ramu, Prinjha Rab K, Upmanyu Ruchi, Kefi Mounir, Zouari Mourad, Sassi Samia Ben, Yahmed Samia Ben, El Euch-Fayeche Ghada, Matthews Paul M, Middleton Lefkos T, Gibson Rachel A, Hentati Fayçal, Farrer Matthew |
| Screening for LRRK2 mutations in patients with Parkinson's disease in Russia: identification of a novel LRRK2 variant. European journal of neurology : the official journal of the European Federation of Neurological Societies 2008 Jul 15 (7): 692-6. Pchelina S N, Yakimovskii A F, Emelyanov A K, Ivanova O N, Schwarzman A L, Singleton A |
| Essential tremor and the common LRRK2 G2385R variant. Parkinsonism & related disorders 2008 Nov 14 (7): 569-71. Tan Eng-King, Lee Jasinda, Lim Hui-Qin, Yuen Yih, Zhao |
| A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease. Journal of neurology, neurosurgery, and psychiatry 2010 Apr 81 (4): 391-5. Nishioka Kenya, Kefi Mounir, Jasinska-Myga Barbara, Wider Christian, Vilariño-Güell Carles, Ross Owen A, Heckman Michael G, Middleton Lefkos T, Ishihara-Paul Lianna, Gibson Rachel A, Amouri Rim, Ben Yahmed Samia, Ben Sassi Samia, Zouari Mourad, El Euch Ghada, Farrer Matthew J, Hentati Fayc |
| Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor. Parkinsonism & related disorders 2010 Feb 16 (2): 132-5. Clark Lorraine N, Kisselev Sergey, Park Naeun, Ross Barbara, Verbitsky Miguel, Rios Eileen, Alcalay Roy N, Lee Joseph H, Louis Elan |
| 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 |
| 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 |
| G2019S mutation of the leucine-rich repeat kinase 2 gene in a cohort of Egyptian patients with Parkinson's disease. Genetic testing and molecular biomarkers 2011 Dec 15 (12): 861-6. Hashad Doaa I, Abou-Zeid Abla A, Achmawy Ghada A, Allah Horeya M O Saad, Saad Marwa |
| Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neuroscience letters 2012 May 516 (2): 207-11. Tian Jin-yong, Guo Ji-feng, Wang Lei, Sun Qi-ying, Yao Ling-yan, Luo Lin-zi, Shi Chang-he, Hu Ya-cen, Yan Xin-xiang, Tang Bei-s |
| Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population. Journal of Alzheimer's disease : JAD 2014 38 (2): 351-7. Anfossi Maria, Colao Rosanna, Gallo Maura, Bernardi Livia, Conidi M Elena, Frangipane Francesca, Vasso Franca, Puccio Gianfranco, Clodomiro Alessandra, Mirabelli Maria, Curcio Sabrina A M, Torchia Giusi, Smirne Nicoletta, Di Lorenzo Raffaele, Maletta Raffaele, Bruni Amalia |
| Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients. General physiology and biophysics 2013 Mar 32 (1): 55-66. Bognar Csaba, Baldovic Marian, Benetin Jan, Kadasi Ludovit, Zatkova Andr |
| The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: clinical and demographic characteristics. Neuroscience letters 2013 Jan . Mabel GE, Virginia P, Paola CD, José PJ, Cecilia CM, Felix MM, Coro PR |
| Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy. Neurobiology of aging 2014 Oct 35 (10): 2422.e1-2. Gagliardi Monica, Annesi Grazia, Tarantino Patrizia, Nicoletti Giuseppe, Quattrone Al |
| Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from Campania. Journal of Parkinson's disease 2014 4 (1): 123-8. De Rosa Anna, De Michele Giuseppe, Guacci Anna, Carbone Rosa, Lieto Maria, Peluso Silvio, Picillo Marina, Barone Paolo, Salemi Fabrizio, Laiso Antonio, Saccà Francesco, Tessitore Alessandro, Pellecchia Maria Teresa, Bonifati Vincenzo, Criscuolo Chia |
| 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 |
| 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 |
| Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease. Journal of the neurological sciences 2017 Oct 381 160-164. da Silva Camilla P, de M Abreu Gabriella, Cabello Acero Pedro H, Campos Mário, Pereira João S, de A Ramos Sarah R, Nascimento Caroline M, Voigt Danielle D, Rosso Ana Lucia, Araujo Leite Marco A, Vasconcellos Luiz Felipe R, Nicaretta Denise H, Della Coletta Marcus V, da Silva Delson José, Gonçalves Andressa P, Dos Santos Jussara M, Calassara Veluma, Valença Débora Cristina T, de M Martins Cyro J, Santos-Rebouças Cíntia B, Pimentel Márcia M |
| 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 |
| Case-control analysis of LRRK2 protective variants in Essential Tremor. Scientific reports 2018 Mar 8 (1): 5346. Ng Adeline S L, Ng Ebonne Y L, Tan Yi Jayne, Prakash Kumar M, Au Wing Lok, Tan Louis C S, Tan Eng-Ki |
| Dynamic interaction of genetic risk factors and cocaine abuse in the background of Parkinsonism - a case report. BMC neurology 2019 10 19 (1): 260. Illés Anett, Balicza Péter, Molnár Viktor, Bencsik Renáta, Szilvási István, Molnar Maria Jud |
| Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
| Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson's Disease Progression. Neuromolecular medicine 2020 10 23 (2): 292-304. Y?lmazer Selma, Canda? Esin, Genç Gençer, Alayl?o?lu Merve, ?engül Bü?ra, Gündüz Ay?egül, Apayd?n Hülya, K?z?ltan Güne?, Ertan Sibel, Dursun Erdinç, Gezen-Ak Duy |
| Heart rate variability and sympathetic skin response for the assessment of autonomic dysfunction in leucine-rich repeat kinase 2 associated Parkinson's disease. Neurophysiologie clinique = Clinical neurophysiology 2022 1 52 (1): 81-93. Nasri Amina, Kacem Imen, Farhat Nouha, Gharbi Alya, Sakka Selma, Souissi Amira, Zidi Sabrina, Damak Mariem, Bendjebara Mouna, Gargouri Amina, Mhiri Chokri, Gouider Ria |
| Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients. Journal of molecular neuroscience : MN 2023 5 . Imane Smaili, Houyam Tibar, Mounia Rahmani, Najlaa Machkour, Rachid Razine, Hajar Naciri Darai, Naima Bouslam, Ali Benomar, Wafa Regragui, Ahmed Bouhouc |
| 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 |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 01, 2023
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