Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ivana Hadacova"'
Autor:
Dagmar Pospisilova, Dusan Holub, Zuzana Zidova, Lucie Sulovska, Jiri Houda, Vladimir Mihal, Ivana Hadacova, Lenka Radova, Petr Dzubak, Marian Hajduch, Vladimir Divoky, Monika Horvathova
Publikováno v:
Haematologica, Vol 99, Iss 7 (2014)
Externí odkaz:
https://doaj.org/article/0bf8e8df7bb646a68d8e1e4437687aa2
Autor:
Agata Kubickova, Zuzana Maceckova, Petr Vojta, Martin Ondra, Jana Volejnikova, Pavla Koralkova, Alexandra Jungova, Ondřej Jahoda, Renata Mojzikova, Ivana Hadacova, Jaroslav Cermak, Monika Horvathova, Dagmar Pospisilova, Marian Hajduch
Publikováno v:
Blood cells, moleculesdiseases. 97
Diamond-Blackfan anemia (DBA) is predominantly underlined by mutations in genes encoding ribosomal proteins (RP); however, its etiology remains unexplained in approximately 25 % of patients. We previously reported a novel heterozygous RPS7 mutation h
Autor:
Jacqueline Halton, Leonardo R Brandão, Matteo Luciani, Lisa Bomgaars, Elizabeth Chalmers, Lesley G Mitchell, Ildar Nurmeev, Anjali Sharathkumar, Pavel Svirin, Kirill Gorbatikov, Igor Tartakovsky, Monika Simetzberger, Fenglei Huang, Zhichao Sun, Jörg Kreuzer, Savion Gropper, Paul Reilly, Martina Brueckmann, Manuela Albisetti, Asiya Safina, Ondrej Zapletal, Tomas Kuhn, Tomas Votava, Judy Felgenhauer, Ali Amid, Paola Saracco, Csongor Kiss, Susan Halimeh, Madlen Reschke, Beate Wulff, Michele David, Zbynek Novak, Inna Trunina, Tony Frisk, Heidi Glosli, Andreas Groll, Olga Lvova, Ilgen Sasmaz, Darintr Sosothikul, Virginija Zilinskaite, Erin Cockrell, Valeriy Digtyar, Ivana Hadacova, Sauli Palmu, Anjali Pawar, Joyce Maria Annichino Bizzacchi, Umran Caliskan, Tiraje Celkan, Dmytro Dmytriiev, Colleen Harkins Druzgal, Graciela Onelda Elena, Antonis Kattamis, Ramazan Kaan Kavakli, Christoph Male, Nihal Ozdemir, An Van Damme, Tatiana Zvereva, Aanen Aarli, Rogelio Alejandro Paredes Aguilera, Selin Aytac, Jorge Carneiro, Antonio Chistolini, Maria Gabriela Mazzucconi, Fernando Corrales-Medina, Francis Couturaud, Stacey E Croteau, Cameron Trenor III, Michael Damgaard, Natalia Dixon, Anna Galustyan, Jiri Hak, Marianne Hoffmann, Alphan Kupesiz, Veerle Labarque, Christel van Geet, Ming-Chih Lin, Yun-Ching Fu, Sandra Loggetto, Veerle Mondelaers, Irena Odri-Komazec, Shoshana Revel-Vilk, Julian Sevilla, Luciano Fuzzato Silva, José Kerr Saraiva, Fernando Felix Montes Tapia, Wendy Woods-Swafford
Publikováno v:
The Lancet. Haematology, Vol. 8, no.1, p. e22-e33 (2021)
BACKGROUND: Dabigatran etexilate is a direct oral anticoagulant with potential to overcome the limitations of standard of care in children with venous thromboembolism. The aims of this clinical trial were to study the appropriateness of a paediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6576a5afe58bf10852f806c3c8eb49
https://hdl.handle.net/2078.1/260410
https://hdl.handle.net/2078.1/260410
Autor:
Ivana Šarbochová, Zuzana Lacinova, Tereza Růžičková, Luděk Táborský, Vojtěch Kaplan, Václav Matʼoška, Martin Šrámek, Ivana Hadacova, Victor L. Serebruany, Aleš Tomek, Petr Janský, Hana Magerova, Alena Frýdmanová, Jaroslava Paulasova-Schwabová
Publikováno v:
American Journal of Therapeutics. 25:e202-e212
BACKGROUND Variable response after clopidogrel is well documented and may affect major adverse clinical events after stroke. Impact of CYP2C19 genetic polymorphisms is an established marker linked to variable response after clopidogrel. However, the
Autor:
Ingrid Hrachovinova, Martin Hruda, Ivana Hadacova, Tomas Binder, Peter Salaj, Blanka Vavrinkova
Publikováno v:
Biomedical Papers. 158:238-241
Objective. To evaluate the course of pregnancy and puerperium in asymptomatic carriers of FV Leiden and FII prothrombin mutation in heterozygous configuration in terms of risk of thrombembolic disease (TED) and late pregnancy complications. To evalua
Publikováno v:
Medicine
Mucormycosis is an aggressive fungal infection, which invades endothelial cells of blood vessels. This condition might lead to destruction of endothelium and release of heparin-like substances to the bloodstream and cause life-threatening bleeding, w
Autor:
Ivana Hadacova, Zuzana Zidova, Monika Horvathova, Petr Dzubak, Dusan Holub, Jiri Houda, Dagmar Pospisilova, Vladimir Divoky, Lucie Sulovska, Vladimír Mihál, Lenka Radová, Marian Hajduch
Publikováno v:
Haematologica
Diamond-Blackfan anemia (DBA) is a rare congenital red cell aplasia associated with mutations in ribosomal proteins (RP) in 49–71% of cases.[1][1] DBA is a clinically heterogeneous disorder with one-third of patients developing transfusion-acquired
Autor:
Ivana Hadacova, Jana Volejnikova, Zuzana Saxova, Pavla Koralkova, Renata Mojzikova, Marian Hajduch, Monika Horvathova, Petr Vojta, Dagmar Pospisilova, Alexandra Jungova, Marie Jarošová, Zuzana Maceckova
Publikováno v:
Blood. 128:3903-3903
The Czech National Diamond-Blackfan Anemia (DBA) Registry currently consists of 51 patients; in 36 of them ribosomal protein (RP) mutations have previously been identified. Targeted sequencing of genes encoding RP, exomes and transcriptomic sequencin
Autor:
Miroslav Durila, Sergej Jurčenko, Martina Pelichovská, Ivana Hadacova, Karel Cvachovec, Tomas Kalincik
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 21(8)
In critically ill patients, either arterial or venous blood is usually available for sampling and measurement of basic coagulation parameters. The aim of this study was to examine whether in these patients the values of coagulation parameters differ