Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Melén B"'
Autor:
Cristina Emilia Ursu, Margit Șerban, Jenel Marian Pătrașcu, Daniel Coriu, Ioana Ioniță, Adina Trăilă, Ciprian Tomuleasa, Delia Săvescu, Melen Brânză, Codruţ Ivan, Teodora Smaranda Arghirescu
Publikováno v:
Life, Vol 14, Iss 9, p 1172 (2024)
Despite the controversies regarding the appropriateness and justification of simultaneous bi- and multi-concomitant surgical procedures, this operative technique is increasingly undertaken for economic reasons. This paper discusses three cases of sim
Externí odkaz:
https://doaj.org/article/2bae3c07c6b143688e76d2083831958c
Autor:
Atanas Banchev, Angelika Bátorová, Ana Boban, Melen Brinza, Barbara Faganel Kotnik, Letitia Pintilie-Ancuta, Ester Zapotocka
Publikováno v:
HemaSphere, Vol 7, p e183378c (2023)
Externí odkaz:
https://doaj.org/article/2cef7fe0d9014c308f941a8ff07b6f4c
Autor:
Ana Boban, Atanas Banchev, Angelika Bátorová, Melen Brinza, Barbara Faganel Kotnik, Letitia Pintilie-Ancuta, Ester Zapotocka
Publikováno v:
HemaSphere, Vol 7, p e10095d7 (2023)
Externí odkaz:
https://doaj.org/article/63a7821df6b6449b8b0bac37845e727f
Publikováno v:
Clinical & Experimental Immunology. Nov1975, Vol. 22 Issue 2, p230-239. 10p.
Autor:
Melen Brinza, Andra Grigore, Mihaela Dragomir, Dumitru Jardan, Cerasela Jardan, Paul Balanescu, Claudia Cristina Tarniceriu, Oana Viola Badulescu, Cristina Blag, Ciprian Tomuleasa, Adina Traila, Margit Serban, Daniel Coriu
Publikováno v:
Medicina, Vol 59, Iss 10, p 1821 (2023)
Background and Objectives: Despite the vast heterogeneity in the genetic defects causing hemophilia A (HA), large intron inversions represent a major cause of disease, accounting for almost half of the cases of severe HA worldwide. We investigated th
Externí odkaz:
https://doaj.org/article/e54957c7546c486cba33e66922c6dd97
Autor:
Melen Brinza, Uscatescu Valentina, Gheorghe Georgiana, Chiriac Elisabeta, Ciobanu Claudia, Orban Horia, Coriu Daniel
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 28, Iss 2, Pp 217-224 (2020)
The development of factor VIII inhibitors (allo-antibodies) continues to be a major complication in the management of severe forms of hemophilia A, especially as far as treatment and treatment response monitoring is concerned. The need to implement a
Externí odkaz:
https://doaj.org/article/e9463b5925e345f680f2f55143c8f598
Autor:
Noemi Dirzu, Ionut Hotea, Ciprian Jitaru, Melen Brinza, Laura Urian, Mareike-Catrina Peters, Krisztina Gal, Louis Popescu, Cristina Blag, Mirela Marian, Eva Pal, Marilena Stanescu, Diana Cenariu, Cristina Tarniceriu, Margit Serban, Delia Dima, Daniel Coriu, Ciprian Tomuleasa
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
The management of patients with hemophilia has evolved significantly since the first treatment attempts were made in the late 1930s. Since then, each new step in the treatment of patients with hemophilia has brought important advancements, as well as
Externí odkaz:
https://doaj.org/article/bf974c7a2f3143509810b4f6bd9bfed2
Autor:
Alina-Andreea Zimta, Ionut Hotea, Melen Brinza, Cristina Blag, Sabina Iluta, Catalin Constantinescu, Atamyrat Bashimov, Elisabeth-Antonia Marchis-Hund, Alexandra Coudsy, Laetitia Muller-Mohnssen, Noemi Dirzu, Diana Gulei, Delia Dima, Margit Serban, Daniel Coriu, Ciprian Tomuleasa
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Hemophilia type A (HA) is the most common type of blood coagulation disorder. While the vast majority of cases are inherited and caused by mutations in the F8 gene, recent data raises new questions regarding the non-heritability of this disease, as w
Externí odkaz:
https://doaj.org/article/1a4b35e6691f46f8a324ba68a98c1d67
Publikováno v:
Acta Paediatrica; Sep1982, Vol. 71 Issue 5, p779-783, 5p
Publikováno v:
Acta Radiologica: Therapy, Physics, Biology; 1974, Vol. 13 Issue 3, p185-200, 16p