Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sarka Blahutova"'
Autor:
Miloš Bohoněk, Jan Máca, Jiří Sagan, David Řezáč, Viktor Fridrich, Anna Burantová, Dominik Kutáč, Pavel Vabroušek, Jan Kubů, Aleš Chrdle, Kateřina Volfová, Šárka Blahutová, Ivan Rychlík, Kateřina Vonášková, Radek Majerčin, Radka Králová, Petr Štěpánek, Michal Holub
Publikováno v:
Virology Journal, Vol 21, Iss 1, Pp 1-8 (2024)
Abstract Purpose Convalescent plasma (CP) collected from people who recovered from COVID-19 became a rapidly available treatment modality in numerous countries, including the Czech Republic. The aims of our study were to evaluate the effectiveness an
Externí odkaz:
https://doaj.org/article/385516b4689049e5b72fbe22c002f689
Autor:
Tomas Papajik, Edgar Faber, Tomáš Szotkowski, Milan Kolář, Lucia Vráblová, Karel Indrak, Sarka Blahutova, Luděk Raida, Zuzana Cermakova, Hubácek J, Peter Rohoň, Renata Urbanova
Publikováno v:
Transfusion Clinique et Biologique. 26:299-303
BACKGROUND There is no universally accepted opinion on the use of granulocyte transfusions collected using apheresis (GTA) in neutropenic patients and severe infection. PATIENTS AND METHODS The efficacy and safety of GTAs transfused at a single cente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc5b62a750a5ba9ac421bf7cfd49641c
https://doi.org/10.1016/j.tracli.2018.09.001
https://doi.org/10.1016/j.tracli.2018.09.001
Autor:
Pavel Polák, Sarka Blahutova, Gabriela Romanová, R. Hrdličková, Marta Zvarová, Jiřina Zavřelová, Miroslav Penka, Petr Smejkal, Libuše Husová
Publikováno v:
Vnitrni lekarstvi. 66(5)
The authors present clinical case of orthotopic liver transplantation for cirhosis due to chronic viral hepatitis C in a subject with severe hemophilia A. Preoperatively performed pharmacokinetic study with recombinant F VIII confirmed satisfactory i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca0f32e5c060f0609ce3390d3d26f84d
https://pubmed.ncbi.nlm.nih.gov/32942877
https://pubmed.ncbi.nlm.nih.gov/32942877
Publikováno v:
Journal of clinical apheresis. 34(1)
BACKGROUND Hereditary thrombotic thrombocytopenic purpura, also called Upshaw-Schulman syndrome (USS), is a rare disease caused by genetic mutations in the ADAMTS13 gene, which severely decrease the activity of ADAMTS13, a metalloprotease that cleave
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dda3119802974af4e6d0b4b11554b173
https://pubmed.ncbi.nlm.nih.gov/31318474
https://pubmed.ncbi.nlm.nih.gov/31318474
Autor:
Dana Galuszkova, Sarka Blahutova, Zuzana Cermakova, Tomas Papajik, Hubácek J, Martina Sommerova
Publikováno v:
Biomedical Papers. 158:309-312
Background. Granulocyte apheresis is a safe and effective method for granulocyte collection. We present a five year experience (2006-2010) of the Blood Center, Faculty Hospital Ostrava, Czech Republic. Donor granulocyte transfusion is one treatment o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867c97da63ec84d11df8082c9e9d1759
https://doi.org/10.5507/bp.2012.071
https://doi.org/10.5507/bp.2012.071
Autor:
R. Hrdličková, Radim Brát, Sarka Blahutova, Jana Dvořáčková, Zuzana Cermakova, Martin Kořístka, I. Valkovský
Publikováno v:
Prague Medical Report, Vol 113, Iss 4, Pp 294-298 (2012)
Transfusion-related acute lung injury (TRALI) is a severe life-threatening complication of blood transfusion, characterized by acute lung injury developing within 2-6 h of transfusion. However, TRALI is difficult to diagnose, and the initial report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::565a1fdf4fbdeee4792fd83edfa70c62
https://doi.org/10.14712/23362936.2015.13
https://doi.org/10.14712/23362936.2015.13
Publikováno v:
Journal of Blood Disorders & Transfusion.
Inherited factor VII (FVII) deficiency is the most frequently observed rare bleeding disorder. The clinical symptoms are extremely variable, and patients may be asymptomatic or may present with life-threatening bleeding disorders. FVII activity (FVII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c94b84debaa02a7c3a23051ff72e0313
https://doi.org/10.4172/2155-9864.1000239
https://doi.org/10.4172/2155-9864.1000239