PREŠOVSKÁ UNIVERZITA V PREŠOVE
UNIVERZITNÁ KNIŽNICA
UNIVERZITNÁ KNIŽNICA
| ID záznamu: | PU.Prešov.2013020610515187 |
|---|---|
| Kategória: | ADC |
| Autor: | Bôžiková Alexandra (50%) |
| Autor: | Dojčáková Dana (10%) |
| Autor: | Sovičová Adriana (5%) |
| Autor: | Behulová Regína (5%) |
| Autor: | Mačeková Soňa (5%) |
| Autor: | Boroňová Iveta (5%) |
| Autor: | Petrejčíková Eva (5%) |
| Autor: | Soták Miroslav (5%) |
| Autor: | Bernasovská Jarmila (5%) |
| Autor: | Bernasovský Ivan (5%) |
| Názov: | The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia [print, elektronický dokument] |
| Zdroj: | Journal of Thrombosis and Thrombolysis [print, elektronický dokument] : a Journal for Translation, Application and Therapeutics in Thrombosis and Vascular Science |
| Lokácia: | Roč. 34, č. 3. - Amsterdam : Kluwer Academic Publishers, (2012), s. 406-409 |
| ISSN: | 0929-5305. - ISSN 1573-742X |
| Ohlas: | [1] 2015. MASINDOVA, I., SOLTYSOVA, A., VARGA, L. et al. MARVELD2 (DFNB49) Mutations in the hearing impaired Central European Roma population - prevalence, clinical impact and the common origin. In PLoS one, ISSN 1932-6203. 2015, vol. 10, no. 4. |
| Ohlas: | [1] 2017. HAMILTON, E.M.C., BERTINI, E., KALAYDJIEVA, L. et al. UFM1 founder mutation in the Roma population causes recessive variant of H-ABC. In Neurology, ISSN 0028-3878. 2017, vol. 89, no. 17, s. 1821-1828. |
| Ohlas: | [1] 2017. DJUROVIC, J., STOJKOVIC, O., BRAJIC, A. et al. Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations. In Human fertility, ISSN 1464-7273. 2017, vol. 20, no. 2, s. 132-139. |
| Ohlas: | [1] 2018. QI, X., HAN, G., GUO, X. et al. Review article: the aetiology of primary Budd–Chiari syndrome – differences between the West and China. In Alimentary pharmacology and therapeutics, ISSN 0269-2813. 2018, vol. 44, no. 11-12, s. 1152-1167. |
| Ohlas: | [1] 2016. DZIADOSZ, M., BAXI, L.V. Global prevalence of prothrombin gene mutation G20210A and implications in women's health: A systematic review. In Blood coagulation and fibrinolysis, ISSN 0957-5235. 2016, vol. 27, no. 5, s. 481-489. |
| Ohlas: | [1] 2019. FIATAL, S., PIKÓ, P., KÓSA, Z. et al. Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. In Thrombosis research, ISSN 0049-3848. 2019, vol. 179, s. 44. |
