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21por Teodoru, Cosmin Adrian, Munteanu, Mihnea, Mercea, Nadina, Moatar, Alina, Stanca, Horia, Popescu, Florina Georgeta, Dura, Horațiu, Hașegan, Adrian, Giurgiu, Doina Ileana, Cerghedean-Florea, Maria-Emilia“…An extensive hypercoagulable panel was completed and we found a positive result for Factor V Leiden (heterozygous mutation) and methyl-enetetrahydrofolate reductase (MTHFR-C677T homozygous mutations). …”
Publicado 2023
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23por Lodigiani, Corrado, Ferrazzi, Paola, Di Micco, Pierpaolo, Librè, Luca, Genovese, Stefano, Quaglia, Ilaria, Rota, Lidia Luciana“…All selected patients were divided in 2 groups: the first group (group A) included 64 patients with previous VTE and carriers of factor V Leiden, while the second group (group B) included 51 patients with previous VTE and evetually carriers of thrombophilic defects other than factor V Leiden. …”
Publicado 2009
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24“…Factor V Leiden mutation, being a hypercoagulable state, posed a higher risk for thromboembolism in this child. …”
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25por Collins, Kenneth“…However, the virtual Padua monopoly on Jewish medical education came to an end during the seventeenth century as the reputation of the Dutch medical school in Leiden grew. For aspiring medieval Jewish physicians Padua was, for around three hundred years, the first, simplest, and usually the only choice.…”
Publicado 2013
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28“…We report a case of multiple brain abscesses in a 51-year-old female with a past medical history significant only for factor V Leiden mutation, and deep vein thrombosis on chronic anticoagulation. …”
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29“…The anatomical collection of the Anatomical Museum of Leiden University Medical Center (historically referred to as Museum Anatomicum Academiae Lugduno‐Batavae) houses and maintains more than 13,000 unique anatomical, pathological and zoological specimens, and include the oldest teratological specimens of The Netherlands. …”
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30“…BACKGROUND AND OBJECTIVE: Thrombophilia is a term used to define the conditions creating a tendency toward thrombosis. Factor V Leiden (FVL) is the most frequently observed genetic risk factor, and its frequency varies among societies and ethnicities. …”
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31por Hasan, AlkomietEnlace del recurso
Publicado 2021
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32por Dusek, Jiri, Nedvedova, Lenka, Scheinost, Ondrej, Hanzl, Milan, Kantorova, Eva, Fendrstatova, Eva, Sram, Radim J., Kotouckova, Hana, Voracek, Jan“…In our research, the occurrence of the V Leiden mutation was found significantly higher in newborns under 1500 g. …”
Publicado 2022
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33por el marraki, Zakaria, bouzhir, Adam, eddhima, Zidane, el bouanani, Alaa-Eddine, mouine, Najat, benyass, Atif“…Genetic risk factors are also present and are dominated by the factor V Leiden mutation, which is present in 20% of VTE and in 2–5% of the general population with an annual incidence of 0.1% (Margaglione and Grandone, 2011; Ridker et al., 1995) [4,5]. …”
Publicado 2022
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34por Kamerlingh Onnes, H and al“….: Communications from the Kamerligh Onnes Laboratory of the University of Leiden…”
Publicado 2002
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35“…Patients were divided into three groups according to the Leiden score: low-risk group (Leiden score <5), medium-risk group (Leiden score 5–20), and high-risk group (Leiden score >20). …”
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36por Inia, José A., Stokman, Geurt, Morrison, Martine C., Worms, Nicole, Verschuren, Lars, Caspers, Martien P. M., Menke, Aswin L., Petitjean, Louis, Chen, Li, Petitjean, Mathieu, Jukema, J. Wouter, Princen, Hans M. G., van den Hoek, Anita M.“…In FFD-fed Ldlr-/-.Leiden control mice, this gene set was upregulated as well, while semaglutide predominantly reversed this gene expression. …”
Publicado 2023
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37“…Although hypercoagulable states are most often associated with venous thromboses, arterial thromboses are reported in protein C, protein S, antithrombin deficient patients and in those with factor V Leiden, components of hereditary thrombophilia. Because these arterial thromboses (peripheral artery disease, myocardial infarction, and cerebral infarction) mostly affect young persons, aged below 45 years, it is important to test and treat these thrombophilic defects. …”
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38por Mooijaart, Simon P., van Heemst, Diana, Noordam, Raymond, Rozing, Maarten P., Wijsman, Carolien A., de Craen, Anton J.M., Westendorp, Rudi G.J., Beekman, Marian, Slagboom, Eline P.“…In humans, type 2 diabetes is a frequent disease that results from loss of glucose homeostasis and for which new candidate polymorphisms now rapidly emerge from genome wide association studies. In the Leiden Longevity Study (n=2415), the offspring of long lived siblings (“offspring”) who are genetically enriched for longevity were shown to have a more beneficial metabolic profile compared to their environmentally matched partners (“controls”), including better glucose tolerance. …”
Publicado 2010
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39por Waaijer, Mariette E. C., Gunn, David A., Catt, Sharon D., van Ginkel, Michael, de Craen, Anton J. M., Hudson, Nicole M., van Heemst, Diana, Slagboom, P. Eline, Westendorp, Rudi G. J., Maier, Andrea B.Enlace del recurso
Publicado 2011
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40por Katzav, Aviva, Grigoriadis, Nikolaos C, Ebert, Tania, Touloumi, Olga, Blank, Miri, Pick, Chaim G, Shoenfeld, Yehuda, Chapman, Joab“…BACKGROUND: We investigated interactions between genetically and autoimmune-mediated coagulopathies by inducing experimental antiphospholipid syndrome (eAPS) in mice carrying the factor V Leiden (FVL) mutation. METHODS: eAPS was induced in heterozygous and homozygous FVL transgenic mice (C57BL/6 background) by immunization with β(2)-glycoprotein I (β(2)-GPI). …”
Publicado 2013
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