Výsledky vyhledávání - "factor v (g1691a)"

Akademický článek

The effects of genetic polymorphisms and diabetes mellitus on the development of peripheral artery disease

Autor: Zafer Yalım, Serap Tutgun Onrat, Sümeyra Alan, Mustafa Aldemir, Alaettin Avşar, İsmet Doğan, Ersel Onrat

Publikováno v: Türk Kardiyoloji Derneği Arşivi, Vol 48, Iss 5, Pp 484-493 (2020)

Objective: Peripheral artery disease (PAD) is a condition caused by the narrowing of limb arteries due to atherosclerosis. In recent years, polymorphisms in a number of genes have been shown to contribute to the risk of PAD development. However, whet

Externí odkaz: https://doaj.org/article/1f3663205ddf46dbb7c9947f6278e9ed

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Akademický článek

Risk factors for deep vein thrombosis of lower extremities in Sudanese women

Autor: Ibrahim NA, Hassan FM, Elgari MM, Abdalla SE

Publikováno v: Vascular Health and Risk Management, Vol Volume 14, Pp 157-164 (2018)

Nadir Ahmed Ibrahim,1,2 Fathelrahman M Hassan,3 Mahmoud Mohamed Elgari,2 Sana Eltahir Abdalla4 1Department of Hematology and Immunohematology, College of Medical Laboratory Science, Sudan University of Science and Technology, Khartoum, Sudan; 2Depart

Externí odkaz: https://doaj.org/article/d86a24dfaaf8476a805c3d9c62df30e4

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Akademický článek

Frequency of Thrombophilic Gene Mutations in Patients with Deep Vein Thrombosis and in Women with Recurrent Pregnancy Loss

Autor: Elgari Mahmoud Mohamed, Ibrahim Nadir Ahmed, Muddathir Abdel Rahim Mahmoud, Eltoom Faris Mergheni, Ibrahim Ibrahim M

Publikováno v: Open Life Sciences, Vol 12, Iss 1, Pp 162-166 (2017)

Thrombophilia may be anticipated by single or combined hereditary defects in encoding genes factor V, Prothrombin, and MTHFR. The aim of this study was to determine the prevalence and associated risks of V Leiden (G1691A), Prothrombin (G20210A), and

Externí odkaz: https://doaj.org/article/3c352395c7cc4c43afbcebf8ea29eec3

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Akademický článek

Evaluation of Genetic and Environmental Risk Factors for Deep Vein Thrombosis in Sudanese

Autor: Nadir Ahmed Ibrahim, Fathelrahman M Hassan Gameel, Mahmoud Mohamed Elgari, Sana Eltahir Abdalla

Publikováno v: Journal of Clinical and Diagnostic Research, Vol 12, Iss 9, Pp GC07-GC10 (2018)

Introduction: Thrombophilia is a multi-factorial hypercoagulability disorder. The predisposing factors may be inherited, acquired or both. Factor V Leiden prothrombin 20210G>A mutations are the most common inherited factors. Aim: This study was aimed

Externí odkaz: https://doaj.org/article/855f9d79067f4e0f8861b5870b60a8f2

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Association of Factor II G20210A, Factor V G1691A and methylenetetrahydrofolate reductase C677T gene polymorphism with different forms of myocardial infarction: ST segment elevation and non-ST segment elevation

Autor: Bojana Cikota-Aleksic, Milica Cucuz-Jokic, Vesna Ilic, Zvonko Magic, Slobodan Obradovic

Publikováno v: Vojnosanitetski Pregled, Vol 77, Iss 10, Pp 1041-1047 (2020)

Background/Aim. Coagulation Factor II G20210A and Factor V G1691A variants are moderately associated with coronary artery disease. Polymorphism of methylenetetrahydrofolate reductase (MTHFR) gene C677T is associated with myocardial infarction (MI) in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02c736424d0a4389a2a46935a895c13
https://doi.org/10.2298/vsp180621170c

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Akademický článek

The importance of studying inherited hematological disorders in ancient Anatolian populations

Autor: Yeşim Doğan Alakoç, Nejat Akar

Publikováno v: Turkish Journal of Hematology, Vol 28, Iss 04, Pp 257-263 (2011)

Before analysis of DNA from ancient remains was possible, anthropologists studied evolution and migration patterns using data obtained from population genetic studies on modern populations combined with data obtained from morphological evaluations of

Externí odkaz: https://doaj.org/article/24f767a9b7194daaa12b3a3869943022

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