Zobrazeno 1 - 10
of 21
pro vyhledávání: '"blood clotting factor 5 Leiden"'
Autor:
Hakan Ekmekçi, Gülnur Tekgöl Uzuner, Burcu Zeydan, Bijen Nazliel, Cemile Handan Misirli, Arda Yilmaz, Ipek Midi, Mehmet Güney Şenol, Nevzat Uzuner, Serkan Demir, Taskin Duman, Mehmet Yaman, Şerefnur Öztürk, Hakan Tekeli, Uygar Utku, Ahmet Tufekci, Nazire Afsar, Necdet Mengulluoglu, Nilufer Yesilot, Mustafa Acikgoz, Baki Göksan, Ozgur Osman Yalin, Firdevs Ezgi Ucan Tokuc, Seden Demirci, Aysel Milanlioglu, Fusun Mayda Domac, Hamit Genc, Mustafa Bakar, Nilgun Cinar, Emrah Aytaç, Nida Tascilar, Sevim Baybaş, Hale Zeynep Batur Caglayan, Sena Colakoglu, Dilek Necioglu Orken, Derya Uluduz, Serdar Oruc, Eylem Ozaydin Goksu, Fatih Ozdag, Vedat Ali Yürekli, Birsen Ince, Hesna Bektas, Yüksel Kablan, Hasan Hüseyin Kozak, Ali Yavuz Karahan, Vildan Yayla, Özge Yilmaz Kuspeci, Hayriye Kucukoglu, Murat Çabalar, Mustafa Gokce, Ufuk Aluclu, Başak Karakurum Göksel
WOS: 000407019200036
PubMed ID: 28583818
Background: Based on a number of small observational studies, cerebral venous sinus thrombosis has diverse clinical and imaging features, risk factors, and variable outcome. In a large, multicenter c
PubMed ID: 28583818
Background: Based on a number of small observational studies, cerebral venous sinus thrombosis has diverse clinical and imaging features, risk factors, and variable outcome. In a large, multicenter c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ebaf578ff170bf919cec8003168e69d
https://avesis.gazi.edu.tr/publication/details/db3708a2-04bc-48af-9f90-2e19e6bfb1d3/oai
https://avesis.gazi.edu.tr/publication/details/db3708a2-04bc-48af-9f90-2e19e6bfb1d3/oai
Autor:
Kucuktasci, K., Semiz, Serap, Balcı, Yasemin Işık, Özsari, T., Gürses, Dolunay, Önem, Gökhan, Saçar, Mustafa, Düzcan, Füsun, Yüksel, Doğangün, Semiz, Ender
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::95ebf7febbc875e0c074fbc38f2d4243
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/9422
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/9422
Autor:
Yasemin Isik Balci, Dolunay Gürses, Serap Semiz, Tamer Özsari, Kazım Küçüktaşçı, Mustafa Saçar, Ender Semiz, Gökhan Önem, Füsun Düzcan, Doğangün Yüksel
Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab2cccfd03e5214223a17b678f87f590
https://hdl.handle.net/11499/9422
https://hdl.handle.net/11499/9422
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 19:574-577
The information about the thromboembolic events, the optimal treatment choice, the dose, and duration of antithrombotic therapy in children are limited. More clinical data are required. Recombinant tissue plasminogen activator (r-tPA) is increasingly
Autor:
Henk-Jan Guchelaar, Tom Schalekamp, A. de Boer, V.H.M. Deneer, Bob Wilffert, L. Grandia, J. van der Weide, Jesse J. Swen, A.H. Maitland-van der Zee, Marga Nijenhuis, Hans Mulder, Gerard A. Rongen, R.H.N. van Schaik, Daan J Touw
Publikováno v:
Clinical Pharmacology & Therapeutics, 89(5), 662-673. Nature Publishing Group
Clinical Pharmacology & Therapeutics, 89(5), 662-673. Wiley-Blackwell
Clinical Pharmacology and Therapeutics, 89, 662-73
Clinical Pharmacology and Therapeutics, 89, 5, pp. 662-73
Clinical Pharmacology & Therapeutics, 89(5), 662-673. Wiley-Blackwell
Clinical Pharmacology and Therapeutics, 89, 662-73
Clinical Pharmacology and Therapeutics, 89, 5, pp. 662-73
Item does not contain fulltext Currently, there are very few guidelines linking the results of pharmacogenetic tests to specific therapeutic recommendations. Therefore, the Royal Dutch Association for the Advancement of Pharmacy established the Pharm
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 13:166-171
Factor V Leiden causing activated protein C resistance is the most common inherited form of thrombophilia leading to thrombosis. Its frequency shows great ethnic and geographic variations. The aim of this study was to determine the frequency of FV Le
Autor:
Soria J.M., Morange P.-E., Vila J., Souto J.C., Moyano M., Trégouët D.-A., Mateo J., Saut N., Salas E., Elosua R.
Publikováno v:
Journal of the American Heart Association
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Background-Genetics plays an important role in venous thromboembolism (VTE). Factor V Leiden (FVL or rs6025) and prothrombin gene G20210A (PT or rs1799963) are the genetic variants currently tested for VTE risk assessment. We hypothesized that primar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::23308ecbd81e53e4f8fe740e0fae4027
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10464
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10464
Publikováno v:
Drug Safety. 36(9)
Introduction: After media attention on thromboembolic adverse drug reactions (ADRs) and the use of cyproterone/ethinylestradiol [1], the Netherlands Pharmacovigilance Centre Lareb received a high number of reports about this association, which called
Acute coronary syndromes (ACS) are one of the leading causes of death and morbidity in industrialized countries. Typical presentation includes acute chest pain, cardiac troponin elevation and possibly associated electrocardiogram abnormalities. In gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::cbbc381ddc79fb7d63104f840b26d974
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/7988
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/7988
Autor:
Mustafa Zungur, Yusuf Izzettin Alihanoglu, Doğu İsmail Kılıç, Halil Tanriverdi, Harun Evrengul
Neurofibromatosis is an autosomal dominant multi-system genetic disorder. Extra-cardiac vascular manifestations of neurofibromatosis have been previously described in many reports. However, coronary arterial involvements have been rarely described. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e66733d97fb36afb56010fc78f61fca
https://doi.org/10.1017/s1047951112000984
https://doi.org/10.1017/s1047951112000984