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pro vyhledávání: '"Lenz, Bahrija"'
Autor:
Bošnjak, Bojana, Drenjančević, Domagoj, Samardžija, Marina, Lenz, Bahrija, Vidović, Sanja, Šljivac, Kristina, Petrak, Daniel, Marijanović, Maja, Perković, Dubravka, Kojić, Branislava
/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::d49b1f902e1b543a16cb663c5ee3d872
https://www.bib.irb.hr/783530
https://www.bib.irb.hr/783530
Akademický článek
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INTRODUCTION: Several lines of evidence indicate a strong causal association between chronic hepatitis C (CHC) and hepatocellular carcinoma (HCC). Hepatocytes are the primary site of HCV replication. The molecular events during hepatocytes proliferat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7d3deef383f6b0aaeed253b4fc57cdc6
https://www.bib.irb.hr/603597
https://www.bib.irb.hr/603597
Autor:
Glasnović, Marija, Bošnjak, Ivica, Včev, Aleksandar, Košuta, Maja, Lenz, Bahrija, Glasnović-Horvatić, Elizabeta
Antifosfolipidni sindrom predstavlja pojavu antifosfolipidnih antitijela, vaskularne tromboze i pojavu problema s reprodukcijom žene. Cilj rada bio je prikazati naša iskustva u dijagnostici i liječenju ovog sindroma. U studiju je uključeno 62 bol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::8477c1e238652ed9c22f65c3ec0c727b
https://www.bib.irb.hr/402099
https://www.bib.irb.hr/402099
At least one thrombophilic mutation was observed in 41.6% of women with pregnancy complications vs. to 20.6% of women with normal pregnancies (p=0.003), factor V Leiden was observed in 15.8% cases and 7.8% controls, prothrombin 20210A in 5.9% cases a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::62713264416b572f3d31a521cc80b239
https://www.bib.irb.hr/388243
https://www.bib.irb.hr/388243
Autor:
Marczi, Saška, Tokić, Stana, Mihaljević, Ivan, Karner, Ivan, Lenz, Bahrija, Glavaš-Obrovac, Ljubica
Introduction: The most significant genetic mutations in coagulation risk factors of thrombosis are factor V G1691A mutation (FV- Leiden), factor II (prothrombin) G20210A mutation, methylenetetrahydrofolate reductase (MTHFR) C677T mutation and plasmin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::2ee9180b48c55d1f752558f38fed309e
https://www.bib.irb.hr/348158
https://www.bib.irb.hr/348158
Autor:
Marczi, Saška, Tokić, Stana, Mihaljević, Ivan, Karner, Ivan, Lenz, Bahrija, Glavaš- Obrovac, Ljubica
Uvod: Najznačajnije genske mutacije koagulacijskih čimbenika rizika za trombozu su G1691A (Leiden mutacija) za faktor V (FV- Leiden), G20210A za faktor II (protrombin), C677T za metilen- tetrahidrofolat reduktazu (MTHFR), te polimorfizam 4G u genu
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https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::2f25d46860e970a3618738f96c211807
https://www.bib.irb.hr/325819
https://www.bib.irb.hr/325819
Autor:
Lenz, Bahrija
We determined the prevalence of factor V Leiden and of prothrombin G20210A mutations in two group of patients referred for suspected deep vein thrombosis (DVT) (n = 94) and arterial thrombosis (AT) (n=36). FVLeiden mutation was defined by the method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::43ac2907cb0521209a4fb0a2f057ef82
https://www.bib.irb.hr/217365
https://www.bib.irb.hr/217365
Akademický článek
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Autor:
Glasnović M; Klinicki odjel za reumatologiju, alergologiju i imunologiju, Klinika za internu medicinu, Josipa Huttlera 4, Osijek. glasnovic.marija@kbo.hr, Bosnjak I, Vcev A, Kosuta M, Lenz B, Glasnović-Horvatić E
Publikováno v:
Reumatizam [Reumatizam] 2008; Vol. 55 (1), pp. 10-5.
