Search Results - "MARINOV, Iuri"

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    FYA silencing by the GATA-motif variant FYA(−69C) in a Caucasian family by Písačka, Martin, Marinov, Iuri, Králová, Miroslava, Králová, Jana, Kořánová, Michaela, Bohoněk, Miloš, Sood, Chhavi, Ochoa-Garay, Gorka

    Published in Transfusion (Philadelphia, Pa.) (01-11-2015)
    “…BACKGROUND The c.1‐67C variant polymorphism in a GATA motif of the FY promoter is known to result in erythroid‐specific FY silencing, that is, in Fy(a−) and…”
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    Journal Article
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    Optimal pretreatment timing for high load dosing (600 mg) of clopidogrel before planned percutaneous coronary intervention for maximal antiplatelet effectiveness by Motovska, Zuzana, Widimsky, Petr, Petr, Robert, Bilkova, Dana, Marinov, Iuri, Simek, Stanislav, Kala, Petr

    Published in International journal of cardiology (08-10-2010)
    “…Abstract Background The optimal timing for 600 mg clopidogrel pre-treatment before planned PCI in patients with stable coronary artery disease has never been…”
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    Clopidogrel resistance "Live" - the risk of stent thrombosis should be evaluated before procedures by Motovska, Zuzana, Widimsky, Petr, Marinov, Iuri, Petr, Robert, Hajkova, Jaroslava, Kvasnicka, Jan

    Published in Thrombosis journal (19-05-2009)
    “…Every year, millions of people undergo percutaneous coronary intervention (PCI) with intracoronary stent implantation. A patient from the PRAGUE-8 trial…”
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    ICCS/ESCCA Consensus Guidelines to detect GPI‐deficient cells in Paroxysmal Nocturnal Hemoglobinuria (PNH) and related Disorders Part 3 – Data Analysis, Reporting and Case Studies by Illingworth, Andrea, Marinov, Iuri, Sutherland, D. Robert, Wagner-Ballon, Orianne, DelVecchio, Luigi

    Published in Cytometry. Part B, Clinical cytometry (01-01-2018)
    “…Over the past several years, a diverse group of physicians and other laboratory scientists have developed various recommendations and guidelines regarding best…”
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    Immunophenotyping of Paroxysmal Nocturnal Hemoglobinuria (PNH) by Illingworth, Andrea J, Marinov, Iuri, Sutherland, D Robert

    “…Paroxysmal nocturnal hemoglobinuria (PNH) is a rare but often debilitating disease which may lead to death in up to 35% of patients within 5 years if…”
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    High‐sensitivity 5‐, 6‐, and 7‐color PNH WBC assays for both Canto II and Navios platforms by Sutherland, D. Robert, Ortiz, Fernando, Quest, Graeme, Illingworth, Andrea, Benko, Miroslav, Nayyar, Rakesh, Marinov, Iuri

    Published in Cytometry. Part B, Clinical cytometry (01-07-2018)
    “…Background Paroxysmal Nocturnal Hemoglobinuria (PNH) is a rare acquired hematopoietic stem cell disorder characterized by an inability to make…”
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    Sensitive and accurate identification of PNH clones based on ICCS/ESCCA PNH Consensus Guidelines—A summary by Illingworth, Andrea J., Marinov, Iuri, Sutherland, D. Robert

    “…Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematopoietic stem cell disorder resulting from the somatic mutation of the X‐linked phosphatidyl‐inositol…”
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    CD71 improves delineation of PNH type III, PNH type II, and normal immature RBCS in patients with paroxysmal nocturnal hemoglobinuria by Sutherland, D. Robert, Richards, Stephen J., Ortiz, Fernando, Nayyar, Rakesh, Benko, Miroslav, Marinov, Iuri, Illingworth, Andrea

    Published in Cytometry. Part B, Clinical cytometry (01-03-2020)
    “…Background The diagnosis of paroxysmal nocturnal hemoglobinuria (PNH) relies on flow cytometric demonstration of loss of glycosyl‐phosphatidyl inositol…”
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    Early MRD response as a prognostic factor in adult patients with acute lymphoblastic leukemia by Šálek, Cyril, Folber, František, Froňková, Eva, Procházka, Bohumír, Marinov, Iuri, Cetkovský, Petr, Mayer, Jiří, Doubek, Michael

    Published in European journal of haematology (01-03-2016)
    “…Objective To evaluate the prognostic power of minimal residual disease (MRD) monitored by polymerase chain reaction at defined time points during early…”
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    Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP by Provaznikova, Dana, Rittich, Simon, Malina, Michal, Seeman, Tomas, Marinov, Iuri, Riedl, Magdalena, Hrachovinova, Ingrid

    “…Atypical hemolytic uremic syndrome (aHUS) is a rare disease characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure…”
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