HuGE Literature Finder
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Records 1-40
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The influence of SLC6A3 and DRD2 polymorphisms on levodopa-therapy in patients with sporadic Parkinson's disease.
The Journal of pharmacy and pharmacology 2019 Feb 71 (2): 206-212. Dos Santos Erinaldo Ubirajara Damasceno, Sampaio Tiago F, Tenório Dos Santos Aléxia D, Bezerra Leite Fernanda C, da Silva Ronaldo C, Crovella Sergio, Asano Amdore Guescel C, Asano Nadja Maria Jorge, de Souza Paulo Roberto |
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DAT gene polymorphisms (rs28363170, rs393795) and levodopa-induced dyskinesias in Parkinson's disease.
Neuroscience letters 2019 01 690 83-88. Purcaro Carlo, Vanacore Nicola, Moret Federica, Di Battista Maria Elena, Rubino Alfonso, Pierandrei Silvia, Lucarelli Marco, Meco Giuseppe, Fattapposta Francesco, Pascale Esteri |
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Suggestive association between OPRM1 and impulse control disorders in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2018 Nov . Cormier-Dequaire Florence, Bekadar Samir, Anheim Mathieu, Lebbah Said, Pelissolo Antoine, Krack Paul, Lacomblez Lucette, Lhommée Eugénie, Castrioto Anna, Azulay Jean-Philippe, Defebvre Luc, Kreisler Alexandre, Durif Franck, Marques-Raquel Ana, Brefel-Courbon Christine, Grabli David, Roze Emmanuel, Llorca Pierre-Michel, Ory-Magne Fabienne, Benatru Isabelle, Ansquer Solene, Maltête David, Tir Melissa, Krystkowiak Pierre, Tranchant Christine, Lagha-Boukbiza Ouhaid, Lebrun-Vignes Bénédicte, Mangone Graziella, Vidailhet Marie, Charbonnier-Beaupel Fanny, Rascol Olivier, Lesage Suzanne, Brice Alexis, Tezenas du Montcel Sophie, Corvol Jean-Christophe, |
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PET imaging of [
European journal of nuclear medicine and molecular imaging 2018 Oct . Varnäs Katarina, Cselényi Zsolt, Jucaite Aurelija, Halldin Christer, Svenningsson Per, Farde Lars, Varrone Andr |
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Functional monoamine oxidase B gene intron 13 polymorphism predicts putaminal dopamine turnover in de novo Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2018 Sep . Löhle Matthias, Mangone Graziella, Wolz Martin, Beuthien-Baumann Bettina, Oehme Liane, van den Hoff Jörg, Kotzerke Jörg, Reichmann Heinz, Corvol Jean-Christophe, Storch Alexand |
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PITX3 genotype and risk of dementia in Parkinson's disease: A population-based study.
Journal of the neurological sciences 2017 Oct 381 278-284. Bäckström David, Domellöf Magdalena Eriksson, Granåsen Gabriel, Linder Jan, Mayans Sofia, Elgh Eva, Mo Susanna Jakobson, Forsgren La |
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No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs.
Attention deficit and hyperactivity disorders 2017 Feb . Geissler Julia M, , Romanos Marcel, Gerlach Manfred, Berg Daniela, Schulte Claud |
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The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review.
Journal of the neurological sciences 2017 Feb 373 23-26. Peng Fang, Sun Yi-Min, Chen Chen, Luo Su-Shan, Li Da-Ke, Wang Yi-Xuan, Yang Ke, Liu Feng-Tao, Zuo Chuan-Tao, Ding Zheng-Tong, An Yu, Wu Jian-Jun, Wang Ji |
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Multiple modality biomarker prediction of cognitive impairment in prospectively followed de novo Parkinson disease.
PloS one 2017 12 (5): e0175674. Caspell-Garcia Chelsea, Simuni Tanya, Tosun-Turgut Duygu, Wu I-Wei, Zhang Yu, Nalls Mike, Singleton Andrew, Shaw Leslie A, Kang Ju-Hee, Trojanowski John Q, Siderowf Andrew, Coffey Christopher, Lasch Shirley, Aarsland Dag, Burn David, Chahine Lana M, Espay Alberto J, Foster Eric D, Hawkins Keith A, Litvan Irene, Richard Irene, Weintraub Daniel, |
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Aging modifies the effect of GCH1 RS11158026 on DAT uptake and Parkinson's disease clinical severity.
Neurobiology of aging 2016 Oct 50 39-46. Webb Joseph, Willette Auriel |
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SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.
Neuroscience letters 2016 Jun . Lu Qian, Song Zhi, Deng Xiong, Xiong Wei, Xu Hongbo, Zhang Zhenmei, Lu Hongwei, Deng H |
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Tryptophan hydroxylase type 2 variants modulate severity and outcome of addictive behaviors in Parkinson's disease.
Parkinsonism & related disorders 2016 May . Cilia Roberto, Benfante Roberta, Asselta Rosanna, Marabini Laura, Cereda Emanuele, Siri Chiara, Pezzoli Gianni, Goldwurm Stefano, Fornasari Die |
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Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2016 Apr . Kraemmer Julia, Smith Kara, Weintraub Daniel, Guillemot Vincent, Nalls Mike A, Cormier-Dequaire Florence, Moszer Ivan, Brice Alexis, Singleton Andrew B, Corvol Jean-Christop |
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Influence of genetic, biological and pharmacological factors on levodopa dose in Parkinson's disease.
Pharmacogenomics 2016 Mar . Altmann Vivian, Schumacher-Schuh Artur F, Rieck Mariana, Callegari-Jacques Sidia M, Rieder Carlos Rm, Hutz Mara |
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DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2?R1441G Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2015 Dec . Bergareche Alberto, Rodríguez-Oroz Maria Cruz, Estanga Ainara, Gorostidi Ana, López de Munain Adolfo, Castillo-Triviño Tamara, Ruiz-Martínez Javier, Mondragón Elisabet, Gaig Carles, Lomeña Francisco, Sarasqueta Cristina, Tolosa Eduardo, Martí-Massó José Fél |
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Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers.
Parkinsonism & related disorders 2015 Aug . Vilas Dolores, Ispierto Lourdes, Álvarez Ramiro, Pont-Sunyer Claustre, Martí María José, Valldeoriola Francesc, Compta Yaroslau, de Fabregues Oriol, Hernández-Vara Jorge, Puente Víctor, Calopa Matilde, Jaumà Serge, Campdelacreu Jaume, Aguilar Miquel, Quílez Pilar, Casquero Pilar, Lomeña Francisco, Ríos José, Tolosa Eduar |
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Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease.
Brain : a journal of neurology 2015 May 138 (Pt 5): 1271-83. Moreau Caroline, Meguig Sayah, Corvol Jean-Christophe, Labreuche Julien, Vasseur Francis, Duhamel Alain, Delval Arnaud, Bardyn Thomas, Devedjian Jean-Christophe, Rouaix Nathalie, Petyt Gregory, Brefel-Courbon Christine, Ory-Magne Fabienne, Guehl Dominique, Eusebio Alexandre, Fraix Valérie, Saulnier Pierre-Jean, Lagha-Boukbiza Ouhaid, Durif Frank, Faighel Mirela, Giordana Caroline, Drapier Sophie, Maltête David, Tranchant Christine, Houeto Jean-Luc, Debû Bettina, Azulay Jean-Philippe, Tison François, Destée Alain, Vidailhet Marie, Rascol Olivier, Dujardin Kathy, Defebvre Luc, Bordet Régis, Sablonnière Bernard, Devos David, |
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Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson's disease.
Brain : a journal of neurology 2014 Nov 137 (Pt 11): 3025-35. Habak Claudine, Noreau Anne, Nagano-Saito Atsuko, Mejía-Constaín Beatriz, Degroot Clotilde, Strafella Antonio P, Chouinard Sylvain, Lafontaine Anne-Louise, Rouleau Guy A, Monchi Ou |
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Sequence variants in SLC6A3, DRD2, and BDNF genes and time to levodopa-induced dyskinesias in Parkinson's disease.
Journal of molecular neuroscience : MN 2014 Jun 53 (2): 183-8. Kaplan Natalie, Vituri Aya, Korczyn Amos D, Cohen Oren S, Inzelberg Rivka, Yahalom Gilad, Kozlova Evgenia, Milgrom Roni, Laitman Yael, Friedman Eitan, Rosset Saharon, Hassin-Baer Shar |
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SLC6A3 is a risk factor for Parkinson's disease: a meta-analysis of sixteen years' studies.
Neuroscience letters 2014 Apr 564 99-104. Zhai Desheng, Li Songji, Zhao Ying, Lin Zhiche |
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Pesticide-induced gene mutations and Parkinson disease risk: a meta-analysis.
Genetic testing and molecular biomarkers 2013 Nov 17 (11): 826-32. Liu Xiaowei, Ma Tao, Qu Bo, Ji Yan, Liu Z |
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Impact of COMT H108L, MAOB int 13 A>G and DRD2 haplotype on the susceptibility to Parkinson's disease in South Indian subjects.
Indian journal of biochemistry & biophysics 2013 Oct 50 (5): 436-41. Kumudini Nadella, Umai Addepally, Devi Yalavarthy Prameela, Naushad Shaik Mohammad, Mridula Rukmini, Borgohain Rupam, Kutala Vijay Kum |
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Radioligand binding to brain dopamine and serotonin receptors and transporters in Parkinson's disease: relation to gene polymorphisms.
The International journal of neuroscience 2012 Mar 122 (3): 124-32. Güzey Cüneyt, Allard Per, Brännström Thomas, Spigset Ol |
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Relationship between SLC6A3 genotype and striatal dopamine transporter availability: a meta-analysis of human single photon emission computed tomography studies.
Synapse (New York, N.Y.) 2011 Oct 65 (10): 998-1005. Costa Anna, Riedel Michael, Müller Ulrich, Möller Hans-Jürge, Ettinger Ulri |
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Smoking, genes encoding dopamine pathway and risk for Parkinson's disease.
Neuroscience letters 2010 Sep 482 (1): 31-4. Gu Zhuqin, Feng Xiuli, Dong Xiumin, Chan P |
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A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.
Movement disorders : official journal of the Movement Disorder Society 2010 May 25 (7): 912-9. De Palma Giuseppe, Dick Finlay D, Calzetti Stefano, Scott Neil W, Prescott Gordon J, Osborne Aileen, Haites Neva, Mozzoni Paola, Negrotti Anna, Scaglioni Augusto, Mutti Antonio, |
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Dopamine transporter genetic variants and pesticides in Parkinson's disease.
Environmental health perspectives 2009 Jun 117 (6): 6. Ritz BR, Manthripragada AD, Costello S, Lincoln SJ, Farrer MJ, Cockburn M, Bronstein J |
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Serotonin and dopamine transporter genes do not influence depression in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009 Jan 24 (1): 111-5. Dissanayaka Nadeeka N W, Silburn Peter A, O'Sullivan John D, Mellick George |
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Polymorphism in environment responsive genes and association with Parkinson disease.
Molecular and cellular biochemistry 2008 May 312 (1-2): 131-8. Singh Madhu, Khan Anwar J, Shah Parag P, Shukla Rakesh, Khanna V K, Parmar Devend |
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Gene-environment interactions in parkinsonism and Parkinson's disease: the Geoparkinson study.
Occupational and environmental medicine 2007 Oct 64 (10): 673-80. Dick F D, De Palma G, Ahmadi A, Osborne A, Scott N W, Prescott G J, Bennett J, Semple S, Dick S, Mozzoni P, Haites N, Wettinger S Bezzina, Mutti A, Otelea M, Seaton A, Soderkvist P, Felice A, |
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Dopamine transporter (SLC6A3) 5' region haplotypes significantly affect transcriptional activity in vitro but are not associated with Parkinson's disease.
Pharmacogenetics and genomics 2005 Sep 15 (9): 659-68. Kelada Samir N, Costa-Mallen Paola, Checkoway Harvey, Carlson Christopher S, Weller Terri-Smith, Swanson Phillip D, Franklin Gary M, Longstreth W T, Afsharinejad Zahra, Costa Lucio |
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Lack of effect of polymorphisms in dopamine metabolism related genes on imaging of TRODAT-1 in striatum of asymptomatic volunteers and patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2003 Jul 18 (7): 804-12. Lynch David R, Mozley P David, Sokol Set, Maas Nicole M C, Balcer Laura J, Siderowf Andrew |
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The homozygote 10-copy genotype of variable number tandem repeat dopamine transporter gene may confer protection against Parkinson's disease for male, but not to female patients.
Journal of the neurological sciences 2003 May 209 (1-2): 87-92. Lin Juei-Jueng, Yueh Kuo-Chu, Chang Dar-Cheng, Chang Chung-Yao, Yeh Yung-Hsiang, Lin Shinn-Zo |
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Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2002 Nov 17 (6): 1305-11. Goudreau John L, Maraganore Demetrius M, Farrer Matthew J, Lesnick Timothy G, Singleton Andrew B, Bower James H, Hardy John A, Rocca Walter |
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Association between dopamine transporter gene polymorphism and susceptibility to Parkinson's disease in Japan.
Movement disorders : official journal of the Movement Disorder Society 2002 Jul 17 (4): 831-2. Nishimura Masataka, Kaji Ryuji, Ohta Mitsuhiro, Mizuta Ikuko, Kuno Sada |
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Association study for Parkinson's disease and a dopamine transporter gene polymorphism (1215A/G).
European neurology 2002 48 (4): 207-9. Lin Chien-Nan, Liu Hsiu-Chih, Tsai Shih-Jen, Liu Tsung-Yun, Hong Chen-J |
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[Association between dopamine transporter gene polymorphism and Parkinson's disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2001 Dec 18 (6): 431-4. Zhang L, Shao M, Xu Q, Dong X, Yang J, Li Y, Chen |
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No evidence of association between a dopamine transporter gene polymorphism (1215A/G) and Parkinson's disease.
Annals of neurology 2001 Feb 49 (2): 276-7. Kimura M, Matsushita S, Arai H, Takeda A, Higuchi |
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[Association between genetic polymorphism of dopamine transporter gene and susceptibility to Parkinson's disease].
Zhonghua yi xue za zhi 2000 May 80 (5): 346-8. Wang J, Liu Z, Chen |
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Dopamine transporter gene polymorphism, spect imaging, and levodopa response in patients with Parkinson disease.
Clinical neuropharmacology 0 27 (3): 111-5. Contin Manuela, Martinelli Paolo, Mochi Mirella, Albani Fiorenzo, Riva Roberto, Scaglione Cesa, Dondi Maurizio, Fanti Stefano, Pettinato Cinzia, Baruzzi Agosti |
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- Page last updated:Nov 14, 2019
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