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901por Rodríguez-Rodríguez, Ignacio, Rodríguez, José-Víctor, Shirvanizadeh, Niloofar, Ortiz, Andrés, Pardo-Quiles, Domingo-Javier“…For this purpose, we used VOSviewer software, which was developed by researchers at Leiden University in the Netherlands. This allowed us to examine the exponential growth in research on this issue and its distribution by country, and to highlight the clear hegemony of the United States (USA) and China in this respect. …”
Publicado 2021
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902por Bellingrath, Julia-Sophia, McClements, Michelle E., Kaukonen, Maria, Fischer, Manuel Dominik, MacLaren, Robert E.“…Pathogenic single nucleotide variants (SNVs) were extracted from the Leiden open-source variation database (LOVD) and ClinVar database and coded by mutational consequence. …”
Publicado 2021
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903por Smits, K., Quint, K.D., Vermeer, M.H., Daniëls, L.A., Willemze, R., Jansen, P.M., Jansen, W.P.A., Neelis, K.J.“…METHODS: In the LUMC, Leiden, we performed a retrospective analysis of 51 patients treated with TSEBT between January 2008 and December 2018, with follow-up untill December 2019. …”
Publicado 2022
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904“…This study is the first to use VOSviewer, a commonly used software tool for constructing and visualizing bibliometric networks and developed by Center for Science and Technology Studies, Leiden University, the Netherlands, to conduct bibliometric analyses on VR-aided therapy from the perspective of Web of Science core collection (WoSc), which objectively and visually shows research structures and topics, therefore offering instructive insights for health care stakeholders (particularly researchers and service providers) such as including integrating more innovative therapies, emphasizing psychological benefits, using game elements, and introducing design research. …”
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905“…HiCBin employs the HiCzin normalization method and the Leiden clustering algorithm and includes the spurious contact detection into binning pipelines for the first time. …”
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906por Yuan, Lushun, Cheng, Shuzhen, Sol, Wendy M.P.J., van der Velden, Anouk I.M., Vink, Hans, Rabelink, Ton J., van den Berg, Bernard M.“…We included blood samples of 32 COVID-19 hospitalised patients at the Leiden University Medical Center, of which 26 were hospitalised in an intensive care unit (ICU) and six on a non-ICU hospital floor; 18 of the samples were obtained from convalescent patients 6 weeks after hospital discharge, and 12 from age-matched healthy donors (control) during the first period of the outbreak. …”
Publicado 2022
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908por Bryen, Samantha J., Yuen, Michaela, Joshi, Himanshu, Dawes, Ruebena, Zhang, Katharine, Lu, Jessica K., Jones, Kristi J., Liang, Christina, Wong, Wui-Kwan, Peduto, Anthony J., Waddell, Leigh B., Evesson, Frances J., Cooper, Sandra T.“…Critical analysis of 24,445 intronic extended acceptor splice-site variants reported in ClinVar and the Leiden Open Variation Database (LOVD) demonstrates 41.9% of pathogenic variants create an AG dinucleotide between the predicted branchpoint and acceptor (AG-creating variants in the AG exclusion zone), 28.4% result in loss of a pyrimidine at the −3 position, and 15.1% result in loss of one or more pyrimidines in the polypyrimidine tract. …”
Publicado 2022
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909por Peeters, Manon H. C. A, Khan, Mubeen, Rooijakkers, Anoek A. M. B, Mulders, Timo, Haer‐Wigman, Lonneke, Boon, Camiel J. F., Klaver, Caroline C. W., van den Born, L. Ingeborgh, Hoyng, Carel B., Cremers, Frans P. M., den Hollander, Anneke I., Dhaenens, Claire‐Marie, Collin, Rob W. J.“…All variants were uploaded into the Leiden Open source Variation and ClinVar databases. …”
Publicado 2021
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910por Kellermair, Lukas, Zeller, Matthias W. G., Kulyk, Caterina, Tomasits, Josef, von Oertzen, Tim J., Vosko, Milan R.“…Up to 30% of all patients with cerebral sinus vein thrombosis (CSVT) are found to have thrombophilic defects such as prothrombin mutation (PTM) or factor V Leiden (FVL). Their repercussions on the plasma levels of dabigatran etexilate are unclear. …”
Publicado 2022
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911por Sherief, Laila M, Zakaria, Marwa, Soliman, Basma K, Kamal, Naglaa M, Alharthi, Sultan A, Abosabie, Sara AS, Abdelazeem, Mahmoud“…The genetic workup for thrombophilia risk identified several genetic thrombophilia mutations: the homozygous factor XIII V34L and MTHFR A1298C mutations and heterozygous factor V Leiden mutation. Three weeks later, the patient was diagnosed with acute lymphoblastic leukemia. …”
Publicado 2022
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912por Hazewinkel, Merel H.J., Berendsen, Remco R., van Klink, Rik C.J., Dik, Hans, Wink, Jeroen, Braun, Jerry, de Lind van Wijngaarden, Robert A.F.“…METHODS: All adult patients undergoing thoracic surgery at the Leiden University Medical Center between January 1, 2016, and December 31, 2017, were reviewed. …”
Publicado 2021
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913“…A case-control study was carried out between June 2019 and April 2020 to examine the correlation between RPL and inherited thrombophilia (IT), namely mutations in factor V Leiden (FVL G1691A), prothrombin (FII G20210A), and methylenetetrahydrofolate reductase (MTHFR C677T). …”
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914por Jokubaitis, Mantas, Mineikytė, Rūta, Kryžauskaitė, Lina, Gumbienė, Lina, Kaplerienė, Lina, Andruškevičius, Saulius, Ryliškienė, Kristina“…Two patients (1.2%) were diagnosed with factor V Leiden mutation, three patients (1.9%) with prothrombin G20210A mutation, one patient (0.6%) had a protein C mutation and one patient (0.6%) had a protein S mutation. …”
Publicado 2022
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916por Rojanaporn, Duangnate, Chitphuk, Sermsiri, Iemwimangsa, Nareenart, Chareonsirisuthigul, Takol, Saengwimol, Duangporn, Aroonroch, Rangsima, Anurathathapan, Usanarat, Hongeng, Suradej, Kaewkhaw, Rossukon“…METHODS: A stepwise method was created on the basis of “hotspot” exons analyzed using data on germline RB1 mutation in the RB1–Leiden Open Variation Database and then tested for mutation screening in the blood DNA of 42 patients with RB. …”
Publicado 2022
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917por Carracedo, Miguel, Pawelzik, Sven‐Christian, Artiach, Gonzalo, Pouwer, Marianne G., Plunde, Oscar, Saliba‐Gustafsson, Peter, Ehrenborg, Ewa, Eriksson, Per, Pieterman, Elsbet, Stenke, Leif, Princen, Hans M. G., Franco‐Cereceda, Anders, Bäck, Magnus“…EXPERIMENTAL APPROACH: Hyperlipidemic APOE*3Leiden.CETP transgenic mice were treated with nilotinib, imatinib or vehicle. …”
Publicado 2022
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918por In het Panhuis, Wietse, Schönke, Milena, Siebeler, Ricky, Afkir, Salwa, Baelde, Rianne, Pronk, Amanda C.M., Streefland, Trea C.M., Sips, Hetty C.M., Lalai, Reshma A., Rensen, Patrick C.N., Kooijman, Sander“…Therefore, we assessed whole-body and BAT energy metabolism in young and middle-aged male and female C57BL/6J mice and studied the consequences for lipid metabolism in humanized APOE*3-Leiden.CETP mice (also on a C57BL/6J background). …”
Publicado 2022
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919por Min, Seung-Kee, Kim, Ji-Sun, Kim, Jang Yong, Park, Ui Jun, Lee, Taehoon, Kang, Jin Mo, Park, Sun Cheol, Choi, Won-Il, Park, Ki-Hyuk, Gebel, Martin“…Interestingly, Koreans showed less accompanying thrombophilia than Caucasians, and factor V Leiden mutations were not detected. Korean analyses comparing the effects of rivaroxaban and standard anticoagulation with primary outcomes showed a lower incidence of major bleeding, recurrent VTE, and all-cause mortality with rivaroxaban. …”
Publicado 2022
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920por Tang, Zihan, Shi, Hui, Liu, Honglei, Cheng, Xiaobing, Su, Yutong, Ye, Junna, Sun, Yue, Hu, Qiongyi, Chi, Huihui, Zhou, Zhuochao, Jia, Jinchao, Meng, Jianfen, Wang, Mengyan, Wang, Fan, Teng, Jialin, Yang, Chengde, Liu, Tingting“…The inherited polymorphisms of the thrombophilic gene, including methylenetetrahydrofolate reductase (MTHFR) C677T, type 1 plasminogen activator inhibitor (PAI-1) 4G/5G, factor V Leiden (FVL) G1691A, prothrombin (PT) G20210A, antithrombin (AT), and fibrinogen (Fg) polymorphisms, were analyzed in 67 aPL(+) patients from the Chinese Han population, including 41 APS patients and 26 persistent aPL carriers. …”
Publicado 2022
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