Cargando…

P1688: VKORC1 -1639 G/A GENE POLYMORPHISM CAN MODULATE THE RISK OF VENOUS THROMBOEMBOLISM IN ELDERLY PATIENTS WITH FV LEIDEN MUTATION

Detalles Bibliográficos
Autores principales:	Kapustin, S., Chechulova, A., Drijun, J., Svitina, S., Burakov, V., Soroka, V., Soldatenkov, V., Papayan, L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Posters
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429324/ http://dx.doi.org/10.1097/01.HS9.0000849608.71108.89

Ejemplares similares

Genetic Polymorphism of VKORC1-1639 in Children With Intracranial Hemorrhage Due to Vitamin K Deficiency
por: Berber, Uğur, et al.
Publicado: (2018)

The impact of VKORC1-1639 G>A polymorphism on the maintenance dose of oral anticoagulants for thromboembolic prophylaxis in North India: A pilot study
por: Rathore, S. S., et al.
Publicado: (2011)

Frequencies of VKORC1-1639G>A and rs397509427 in Patients on Warfarin and Healthy Syrian Subjects
por: Altawil, Yara, et al.
Publicado: (2023)

G-1639A but Not C1173T VKORC1 Gene Polymorphism Is Related to Ischemic Stroke and Its Various Risk Factors in Ukrainian Population
por: Dubovyk, Yevhen I., et al.
Publicado: (2016)

The relationship between FV Leiden and pulmonary embolism
por: Hooper, W Craig, et al.
Publicado: (2002)

Warfarin Dosing in a Patient with CYP2C9(∗)3(∗)3 and VKORC1-1639 AA Genotypes
por: Johnson, Mark, et al.
Publicado: (2014)

Value of VKORC1 (−1639G>A) rs9923231 genotyping in predicting warfarin dose: A replication study in South Indian population
por: Harikrishnan, S., et al.
Publicado: (2018)

Hyper-responsiveness to warfarin in a young patient with the VKORC1 -1639GA/CYP2C9*1*46 genotype: a case report
por: Aldiban, Weam, et al.
Publicado: (2022)

Genome-Wide Investigation of DNA Methylation Marks Associated with FV Leiden Mutation
por: Aïssi, Dylan, et al.
Publicado: (2014)

La Revolución Inglesa, 1688-1689
por: Trevelyan, George Macaulay, 1876-1962
Publicado: (1951)

The History of the College Library 1688—1727
por: Payne, L. M., et al.
Publicado: (1971)

A PCR method for VKORC1 G-1639A and CYP2C9 A1075C genotyping useful to warfarin therapy among Japanese
por: Tamura, Takashi, et al.
Publicado: (2014)

Analysis of 363 Genetic Variants in F5 via an Interactive Web Database Reveals New Insights into FV Deficiency and FV Leiden
por: Efthymiou, Christos, et al.
Publicado: (2023)

Analysis of CYP2C9*2, CYP2C9*3 and VKORC1 -1639 G>A polymorphisms in a population from South-Eastern Europe
por: Buzoianu, Anca D, et al.
Publicado: (2012)

The effect of CYP2C9*2, CYP2C9*3, and VKORC1-1639 G>A polymorphism in patients under warfarin therapy in city of Kermanshah
por: Hosseinkhani, Zohreh, et al.
Publicado: (2018)

Risk of venous thromboembolism in association with factor V leiden in cancer patients – The EDITH case-control study
por: Heraudeau, Adeline, et al.
Publicado: (2018)

Factor V Leiden, estrogen, and multimorbidity association with venous thromboembolism in a British-South Asian cohort
por: Magavern, Emma F., et al.
Publicado: (2023)

A Successful Mother and Neonate Outcome for a Woman with Essential Thrombocytosis and FV Leiden Heterozygosity
por: Politou, Marianna, et al.
Publicado: (2016)

The role of CYP2C9*2, CYP2C9*3 and VKORC1-1639 variants on the susceptibility of upper gastrointestinal bleeding: A full case-control study
por: Forgerini, Marcela, et al.
Publicado: (2023)

1688. Invasive Ocular Candidiasis: Who Is Really at Risk?
por: Seidelman, Jessica, et al.
Publicado: (2019)

A case-control study on factor V Leiden: an independent, gender-dependent risk factor for venous thromboembolism
por: Takhviji, Vahideh, et al.
Publicado: (2021)

Systematic Review and Meta-Analysis of the Susceptibility of ABO Blood Groups to Venous Thromboembolism in Individuals with Factor V Leiden
por: Bawazir, Waleed M.
Publicado: (2022)

Association of venous thromboembolism and myocardial infarction with Factor V Leiden and Factor II gene mutations among Libyan patients
por: Msalati, Abdulghani, et al.
Publicado: (2021)

The Combined Heterozygosity of Factor V Leiden and G20210A Prothrombin Gene Mutation in a Patient With Venous Thromboembolism
por: Machado, Marcia, et al.
Publicado: (2023)

P1679: GENETIC POLYMORPHISM OF PLASMA HEMOSTATIC FACTORS AND THE RISK OF DEEP VEIN THROMBOSIS IN ELDERLY AND SENILE PATIENTS
por: Chechulova, A.
Publicado: (2022)

Current Knowledge on Factor V Leiden Mutation as a Risk Factor for Recurrent Venous Thromboembolism: A Systematic Review and Meta-Analysis
por: Eppenberger, Daria, et al.
Publicado: (2022)

Cytochrome P450 (CYP2C9*2,*3) & vitamin-K epoxide reductase complex (VKORC1 -1639G<A) gene polymorphisms & their effect on acenocoumarol dose in patients with mechanical heart valve replacement
por: Kaur, Anupriya, et al.
Publicado: (2013)

Prevention and treatment of venous thromboembolism in the elderly patient
por: Tincani, Enrico, et al.
Publicado: (2007)

Venous thromboembolism in laparoscopic surgery: experience in elderly
por: Compagna, Rita, et al.
Publicado: (2013)

Origins and Evolutionary Patterns of the 1.688 Satellite DNA Family in Drosophila Phylogeny
por: de Lima, Leonardo G., et al.
Publicado: (2020)

Response Regulator CD1688 Is a Negative Modulator of Sporulation in Clostridioides difficile
por: Kempher, Megan L., et al.
Publicado: (2022)

1639. Outbreak of Human Bartonellosis Due to Bartonella bacilliformis in the Ecuadorian Andes
por: Santiago Larreategui Romero, David, et al.
Publicado: (2019)

Primary prevention of venous thromboembolism in elderly medical patients
por: Lacut, Karine, et al.
Publicado: (2008)

P1688: LIVING WITH ACUTE LEUKEMIA: A GLOBAL SURVEY OF PATIENTS AND CARERS EXPERIENCE
por: Nier, Samantha, et al.
Publicado: (2023)

1639P Impact of COVID-19 on ongoing oncological and hematological treatment strategy
por: Bayle, A., et al.
Publicado: (2021)

High prevalence of protein C, protein S, antithrombin deficiency, and Factor V Leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident
por: Ali, Nadir, et al.
Publicado: (2014)

Variation in VKORC1 Is Associated with Vascular Dementia
por: Mur, Jure, et al.
Publicado: (2021)

First Complete Genome Sequence of Currently Circulating Infectious Bronchitis Virus Strain DMV/1639 of the GI-17 Lineage
por: Goraichuk, Iryna V., et al.
Publicado: (2019)

The Cumulative Incidence and Risk Factors of Recurrent Venous Thromboembolism in the Elderly
por: Aleidan, Fahad A S
Publicado: (2020)

Association between cardiovascular risk factors and venous thromboembolism in the elderly
por: Wang, Huijie, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_avprb5fv88b17qfu6uu326hce5