Zobrazeno 1 - 10
of 222
pro vyhledávání: '"Prothrombin G20210A mutation"'
Autor:
Vlădăreanu Ana-Maria, Onisâi Minodora, Iordan Iuliana, Radu Eugen, Roşca Adrian, Munteanu Octavian, Soare Dan Sebastian, Mambet Cristina, Voiculescu Suzana Elena, Bumbea Horia, Voican Irina, Nicolescu Anca, Mititelu Alina, Nistor Raluca, Secară Diana, Băicuș Anda, Cîrstoiu Monica
Publikováno v:
Türk Biyokimya Dergisi, Vol 49, Iss 1, Pp 138-147 (2023)
To assess the frequency of multiple thrombophilia-associated mutations and polymorphisms in a selected population of high-risk pregnancies.
Externí odkaz:
https://doaj.org/article/ec63a3a8c63146c0a2cb3677a16f4532
Publikováno v:
Thrombosis Journal, Vol 19, Iss 1, Pp 1-8 (2021)
Abstract Objective To study the association between high activity of Factor II (prothrombin) in blood plasma with G20210A mutation and the development of great obstetrical syndromes. Material and methods A prospective clinical cohort study was conduc
Externí odkaz:
https://doaj.org/article/105a204ad8a847e5a7ac6f57e84f0df8
Autor:
M. O. Arslanbekova, J. Kh. Khizroeva
Publikováno v:
Акушерство, гинекология и репродукция, Vol 14, Iss 1, Pp 89-93 (2020)
Here we describe a clinical case of successfully managed pregnancy and labor in female with multigenic thrombophilia (combination of homozygous Leiden and heterozygous prothrombin G20210A mutations) associated with high risk of thrombosis by using pr
Externí odkaz:
https://doaj.org/article/217ffda1a30940ecb585db6b6b79746b
Autor:
Hafize Nalan Güneş
Publikováno v:
Van Tıp Dergisi, Vol 25, Iss 2, Pp 132-137 (2018)
INTRODUCTION: Ischemic stroke remains an important public health problem in all over world. It is wellknown that, some type of genetic mutations such as factor V Leiden and prothrombin G20210A contribute to the risk of ischemic venous stroke. However
Externí odkaz:
https://doaj.org/article/286dd3494f3b4088b7d262faa4633436
Autor:
Madina Arslanbekova, J. Kh. Khizroeva
Publikováno v:
Акушерство, гинекология и репродукция, Vol 14, Iss 1, Pp 89-93 (2020)
Here we describe a clinical case of successfully managed pregnancy and labor in female with multigenic thrombophilia (combination of homozygous Leiden and heterozygous prothrombin G20210A mutations) associated with high risk of thrombosis by using pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c08590eca2a4511a80657fb87268d81
https://doi.org/10.17749/2313-7347.2020.14.1.89-93
https://doi.org/10.17749/2313-7347.2020.14.1.89-93
Autor:
Stoeva Natalia Y., Koleva Vessela S.
Publikováno v:
Folia Medica, Vol 58, Iss 1, Pp 64-66 (2016)
Prothrombin 20210 G>A mutation is the second most frequent inherited factor increasing the risk for developing venous thromboembolism (VTE). The risk for VTE in homozygous carriers of this mutation is not well studied because of their rarity are rare
Externí odkaz:
https://doaj.org/article/7e1f15b462254f848ee8158c56b3ec2e
Akademický článek
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Publikováno v:
Case Reports in Ophthalmology, Vol 3, Iss 1, Pp 61-64 (2012)
We report the first case of nonarteritic anterior ischemic neuropathy (NAION) associated with double thrombophilia: protein S deficiency and prothrombin G20210A mutation. A 58-year-old man is presented including the clinical and laboratory findings,
Externí odkaz:
https://doaj.org/article/4459f7e9e573411c9bed63a9548b476e
Autor:
Luis Klaus A. da Rocha, Nelson Zocoler Galante, Vivian Angélica Castilho Alvarez, Kelsy C. N. Areco, Maria Aparecida E. Noguti, Rogério Q. Amaral, Luis Eduardo C. Andrade, Clóvis Araujo Peres, José O. Medina Pestana, Dayse M. Lourenço
Publikováno v:
Brazilian Journal of Nephrology, Vol 31, Iss 4, Pp 277-285 (2009)
INTRODUÇÃO: Complicações tromboembólicas são importantes fatores de risco para perda do enxerto e pior evolução após o transplante renal. Pacientes com defeito trombofílico apresentam maior risco de complicações tromboembólicas. Foram an
Externí odkaz:
https://doaj.org/article/6351a047b91a41c880b588a95020cb05
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 31, Iss 3, Pp 143-146 (2009)
Thrombosis is a result of the interaction between predisposing genetic polymorphisms and acquired risk factors. The two prothrombotic polymorphisms which are most frequently associated with thrombosis are factor V (FV) Leiden and the prothrombin (PT)
Externí odkaz:
https://doaj.org/article/169c3b1d2cf74e8299958a80e1eaf670