Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Factor V Leiden (FVL)"'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 24, Iss 2, Pp 49-54 (2022)
Venous thromboembolism (VTE) is one of the major causes of pregnancy-related mortality and morbidity. This study aimed to determine the frequency of factor V Leiden (FVL) and prothrombin G20210A polymorphisms and measure the plasma levels of protein
Externí odkaz:
https://doaj.org/article/a2062860b3db439783eafe0c5727ac66
Publikováno v:
Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 43-50 (2016)
The 1691 (G>A) factor V Leiden (FVL) and 20210 (G>A) prothrombin (PT) mutations are the two most common genetic risk factors in venous thromboembolism. The 677 (C>T) methylene tetrahydrofolate reductase (MTHFR) mutation is the most frequently mention
Externí odkaz:
https://doaj.org/article/73308dd7dcc34979b1dc510e526c9eee
Autor:
Hatip Aydin, Resul Arisoy, Ali Karaman, Arda Çetinkaya, Emre Erdoğdu, Oya Demirci, Mehmet Burak Mutlu
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 3, Iss 3, Pp 112-116 (2015)
AimExact etiology of multifactorial anencephaly is still unclear. For a better understanding of the etiology, we sought to determine serum levels of folate and vitamin B12 as well as genetic variations including Factor V Leiden, Factor II g.20210G>A,
Externí odkaz:
https://doaj.org/article/286e2da0725d457ab1b306417b92f7d2
Autor:
Al-Otaiby, Maram, Althnayan, Rahaf, Binmethem, Alanoud, AlEnezy, Reema Bader, Alhadlg, Munira Abdulrahman, Alaqeel, Arjuwana, AlQahtani, Sara H, Ghufran, Noman, Alotaibi, Abdulaziz A., Alayed, Nada, Ali Khan, Imran
Publikováno v:
Nagoya Journal of Medical Science. 83(3):407-417
Arg506Gln mutation is responsible for one of the procoagulant factors and most common inherited thrombophilia in the Factor V Leiden (FVL) family. The replacement of the missense mutation for Arg506Gln / R506Q is at 1691st position from Guanine to Ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::3a3db8580a3ec55a915a4d6c7f871876
https://nagoya.repo.nii.ac.jp/records/2001435
https://nagoya.repo.nii.ac.jp/records/2001435
Autor:
Maram, Al-Otaiby, Rahaf, Althnayan, Alanoud, Binmethem, Reema Bader, AlEnezy, Munira Abdulrahman, Alhadlg, Arjuwana, Alaqeel, Sara H, AlQahtani, Noman, Ghufran, Abdulaziz A, Alotaibi, Nada, Alayed, Imran, Ali Khan
Publikováno v:
Nagoya Journal of Medical Science
Arg506Gln mutation is responsible for one of the procoagulant factors and most common inherited thrombophilia in the Factor V Leiden (FVL) family. The replacement of the missense mutation for Arg506Gln / R506Q is at 1691st position from Guanine to Ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6a72aac9c358fb73a2e3bcc56302efd9
http://europepmc.org/articles/PMC8438009
http://europepmc.org/articles/PMC8438009
Akademický článek
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Akademický článek
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Publikováno v:
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 43-50 (2016)
Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 43-50 (2016)
The 1691 (G>A) factor V Leiden (FVL) and 20210 (G>A) prothrombin (PT) mutations are the two most common genetic risk factors in venous thromboembolism. The 677 (C>T) methylene tetrahydrofolate reductase (MTHFR) mutation is the most frequently mention
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca8e7fffc1a42f0a34bcf041ddde7798
https://doi.org/10.1515/bjmg-2016-0006
https://doi.org/10.1515/bjmg-2016-0006
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
SVEINSDOTTIR, SIGNY
Venous thromboembolism (VTE) is a relatively common cause of morbidity and mortality. It has an annual incidence of around 0.1- 0.3%. It is a multifactorial disease with many known risk factors, both transient and persistent. Among these, several gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1110::40e25d77ec673fee4b774d953d6493e9
https://lup.lub.lu.se/record/a3408b4d-47e8-4820-8b1b-fc8556348e52
https://lup.lub.lu.se/record/a3408b4d-47e8-4820-8b1b-fc8556348e52
