Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Danijela Mikovic"'
Autor:
Raffaella Rossio, Luca Andrea Lotta, Silvia Pontiggia, Nicolò Ghiringhelli Borsa, Isabella Garagiola, Gianluigi Ardissino, Danijela Mikovic, Massimo Cugno, Flora Peyvandi
Publikováno v:
Haematologica, Vol 100, Iss 3 (2015)
Externí odkaz:
https://doaj.org/article/3054a35e73ef4caeacdd991747d65645
Autor:
Flora Peyvandi, Silvia Lavoretano, Roberta Palla, Hendrik B. Feys, Karen Vanhoorelbeke, Tullia Battaglioli, Carla Valsecchi, Maria Teresa Canciani, Fabrizio Fabris, Samo Zver, Marienn Réti, Danijela Mikovic, Mehran Karimi, Gaetano Giuffrida, Luca Laurenti, Pier Mannuccio Mannucci
Publikováno v:
Haematologica, Vol 93, Iss 2 (2008)
Background From 20 to 50% of patients who survive an acute episode of the acquired form of thrombotic thrombocytopenic purpura relapse but clinical and laboratory markers of recurrence are not well established.Design and Methods In 109 patients enrol
Externí odkaz:
https://doaj.org/article/9966c9a66b2142b9a073b81997e42638
Autor:
Roza Chaireti, Danijela Mikovic, David E. Schmidt, Maria Bruzelius, Nida Mahmoud Hourani Soutari, Liselotte Onelöv, Annelie Strålfors, Margareta Holmström, Maria Berndtson, Jovan P. Antovic
Publikováno v:
Thrombosis and Haemostasis. 121:027-035
Background Factor VIII (FVIII) activity (FVIII:C) can be measured by different methods including one-stage clotting assays (OSAs) and chromogenic assays (CSAs). Discrepancy between FVIII:C assays is known and associated with genetic variations causin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ebf102feec131e4101e5eb3cd73157
https://doi.org/10.1055/s-0040-1715443
https://doi.org/10.1055/s-0040-1715443
Publikováno v:
Thrombosis Research. 173:1-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ff226dce339d4a9f7678fef900c27cd
https://doi.org/10.1016/j.thromres.2018.11.008
https://doi.org/10.1016/j.thromres.2018.11.008
Autor:
Barbara Ferrari, Roberta Palla, Andrea Artoni, Flora Peyvandi, Carla Valsecchi, Silvia Pontiggia, Danijela Mikovic, Ilaria Mancini
Publikováno v:
Thrombosis and haemostasis. 119(5)
Acquired thrombotic thrombocytopenic purpura (TTP) is a rare thrombotic microangiopathy caused by the immune-mediated severe deficiency of ADAMTS13. We hereby report the demographic and disease-related data of acquired TTP patients recorded in the Mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f21aa44d63624e8381d36b16ff98469c
https://pubmed.ncbi.nlm.nih.gov/30861548
https://pubmed.ncbi.nlm.nih.gov/30861548
Publikováno v:
Inherited Bleeding Disorders in Women 2e ISBN: 9781119426080
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10d165b7cd1df36db1a8d9996ada5f20
https://doi.org/10.1002/9781119426080.ch8
https://doi.org/10.1002/9781119426080.ch8
Publikováno v:
Seminars in Thrombosis and Hemostasis. 41:903-906
Maintaining the tradition of past events, the 18th International Meeting of the Danubian League against Thrombosis and Haemorrhagic Disorders (DLTH) was held in the multicultural and fascinating city of Sarajevo, Bosnia and Herzegovina, from May 14 t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e00b83fe9d856762e48ab43e3b1af5b
https://doi.org/10.1055/s-0035-1564803
https://doi.org/10.1055/s-0035-1564803
Publikováno v:
Haemophilia. 20:71-75
Rare bleeding disorders (RBDs) are inherited deficiencies of coagulation factors such as fibrinogen, factor (F) II, FV, FVII, combined FV+FVIII, FX, FXI and FXIII. These disorders usually have a low prevalence in the general population and constitute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e2b7b72680a1eedaa87d51a04b2e1b
https://doi.org/10.1111/hae.12402
https://doi.org/10.1111/hae.12402
Autor:
Carla Valsecchio, Flora Peyvandi, Dragica Vucelic, Slobodan Obradovic, Dragana Jevtić, Nebojsa Antonijevic, Zoran Rajić, Nebojsa Savic, Danijela Mikovic, R. Palla, Zivko Budisin
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 141, Iss 7-8, Pp 466-474 (2013)
Introduction. The significance of ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin motif-13) activity for diagnosis and therapy of thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS) is still a controversial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43b75a854d7f325a3aff189b03988623
https://doi.org/10.2298/sarh1308466v
https://doi.org/10.2298/sarh1308466v
Autor:
Maria Berndtsson, Ivo Elezovic, Margareta Holmström, Jovan P. Antovic, Danijela Mikovic, Nida Mahmoud Hourani Soutari, Eva Zetterberg
Publikováno v:
Thrombosis research. 144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3dc388ce0b9b20888172dc34a0489d3
https://pubmed.ncbi.nlm.nih.gov/27331346
https://pubmed.ncbi.nlm.nih.gov/27331346