The 3’ End Prothrombin Gene Variants in Serbian Patients with Idiopathic Thrombophilia

Autor: Aradjanski M., Djordjevic V., Pruner I., Tomic B., Gvozdenov M., Kovac M., Radojkovic D.

Publikováno v: Balkan Journal of Medical Genetics, Vol 17, Iss 2, Pp 43-48 (2014)

Thrombophilia is a multifactorial disorder that arises from the interaction of acquired and genetic risk factors. Despite the significant efforts made to understand the etiology of this disease, there are still a certain number of patients suffering

Externí odkaz: https://doaj.org/article/e1c63f7347324e0290c861ed131e9585

Association of the methionine sulfoxide reductase A rs10903323 gene polymorphism with functional activity and oxidative modification of alpha-1-antitrypsin in COPD patients

Autor: Milovanovic, V., Topic, A., Milinkovic, N., Lazic, Z., Ivosevic, A., Radojkovic, D., Rankov, A. Divac

Publikováno v: In Pulmonology March-April 2024 30(2):122-129

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Clinical and biochemical characterization of the prothrombin Belgrade mutation in a large Serbian pedigree: new insights into the antithrombin resistance mechanism

Autor: Miljic, P., Gvozdenov, M., Takagi, Y., Takagi, A., Pruner, I., Dragojevic, M., Tomic, B., Bodrozic, J., Kojima, T., Radojkovic, D., Djordjevic, V. ^*

Publikováno v: In Journal of Thrombosis and Haemostasis April 2017 15(4):670-677

Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (European Journal of Human Genetics, (2022), 30, 5, (493-495), 10.1038/s41431-021-01000-x)

Autor: Forzano, F., Antonova, O., Clarke, A., de Wert, G., Hentze, S., Jamshidi, Y., Moreau, Y., Perola, M., Prokopenko, I., Read, A., Reymond, A., Stefansdottir, V., van El, C., Genuardi, M., Maurizio, G., Peterlin, B., Oliveira, C., Writzl, K., Houge, G.D., Cordier, C., Howard, H., Macek, M., Melegh, B., Mendes, A., Radojkovic, D., Rial-Sebbag, E., Stefánsdottir, V., Ulph, F.

Publikováno v: Forzano, F, Antonova, O, Clarke, A, de Wert, G, Hentze, S, Jamshidi, Y, Moreau, Y, Perola, M, Prokopenko, I, Read, A, Reymond, A, Stefansdottir, V, van El, C, Genuardi, M, Maurizio, G, Peterlin, B, Oliveira, C, Writzl, K, Houge, G D, Cordier, C, de Wert, G, Howard, H, Macek, M, Melegh, B, Mendes, A, Radojkovic, D, Rial-Sebbag, E, Stefánsdottir, V, Ulph, F & van El, C 2022, ' Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (European Journal of Human Genetics, (2022), 30, 5, (493-495), 10.1038/s41431-021-01000-x) ', European Journal of Human Genetics . https://doi.org/10.1038/s41431-022-01067-0

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3818::e2e114c673b14919c8594654eb325917
https://doi.org/10.1038/s41431-022-01067-0