Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Thromboembolism and APOE[original query] |
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Prevalence of prothrombotic polymorphisms in Greece. Genetic testing 2008 Dec 12 (4): 541-7. Gialeraki Argyri, Politou Marianna, Rallidis Loukianos, Merkouri Efrosyni, Markatos Christos, Kremastinos Dimitrios, Travlou Ant |
Genetic determinants of warfarin dosing in the Han-Chinese population. Pharmacogenomics 2009 Dec 10 (12): 1905-13. Lee M T Michael, Chen Chien-Hsiun, Chou Ching-Heng, Lu Liang-Suei, Chuang Hui-Ping, Chen Ying-Ting, Saleem Amir N, Wen Ming-Shien, Chen Jin-Jer, Wu Jer-Yuarn, Chen Yuan-Tso |
Efficiency and effectiveness of the use of an acenocoumarol pharmacogenetic dosing algorithm versus usual care in patients with venous thromboembolic disease initiating oral anticoagulation: study protocol for a randomized controlled trial. Trials 2012 Dec 13 (1): 1. Carcas AJ, Borobia AM, Velasco M, Abad-Santos F, Díaz MQ, Fernández-Capitán C, Ruiz-Giménez N, Madridano O, Sillero PL |
Prediction of stable acenocoumarol dose by a pharmacogenetic algorithm. Pharmacogenetics and genomics 2014 Oct 24 (10): 501-13. Jiménez-Varo Enrique, Cañadas-Garre Marisa, Gutiérrez-Pimentel María J, Calleja-Hernández Miguel |
Pharmacogenetics role in the safety of acenocoumarol therapy. Thrombosis and haemostasis 2014 Sep 112 (3): 522-36. Jiménez-Varo E, Cañadas-Garre M, Henriques C I, Pinheiro A M, Gutiérrez-Pimentel M J, Calleja-Hernández M |
Polymorphisms of CYP2C9, VKORC1, MDR1, APOE and UGT1A1 genes and the therapeutic warfarin dose in Brazilian patients with thrombosis: a prospective cohort study. Molecular diagnosis & therapy 2014 Dec 18 (6): 675-83. de Oliveira Almeida Vanessa Cristina, Ribeiro Daniel Dias, Gomes Karina Braga, Godard Ana Lúcia Brunial |
Bleeding predictors in patients following venous thromboembolism treated with vitamin K antagonists: Association with increased number of single nucleotide polymorphisms. Vascular pharmacology 2018 Feb . Bryk Agata Hanna, Wypasek Ewa, Plens Krzysztof, Awsiuk Magdalena, Undas Anet |
Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women. Alzheimer's & dementia : the journal of the Alzheimer's Association 2020 9 17 (2): 215-225. Blue Elizabeth E, Thornton Timothy A, Kooperberg Charles, Liu Simin, Wactawski-Wende Jean, Manson JoAnn, Kuller Lew, Hayden Kathleen, Reiner Alexander |
Apolipoprotein E (APOE) genotype-associated disease risks: a phenome-wide, registry-based, case-control study utilising the UK Biobank. EBioMedicine 2020 Aug 59 102954. Lumsden Amanda L, Mulugeta Anwar, Zhou Ang, Hyppönen Eli |
Acenocoumarol Pharmacogenetic Dosing Algorithm versus Usual Care in Patients with Venous Thromboembolism: A Randomised Clinical Trial. Journal of clinical medicine 2021 7 10 (13): . Tong Hoi Yan, Borobia Alberto M, Quintana-Díaz Manuel, Fabra Sara, González-Viñolis Manuel, Fernández-Capitán Carmen, Rodriguez-Dávila María A, Lorenzo Alicia, López-Parra Ana María, Ruiz-Giménez Nuria, Abad-Santos Francisco, Suarez Carmen, Madridano Olga, Gómez-Cerezo Jorge Francisco, Llamas Pilar, Baeza-Richer Carlos, Arroyo-Pardo Eduardo, Carcas Antonio J, The Pgx-Ace Spanish Investigators Grou |
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