Search Results - "Krejčí, Martin"

Lymphangiomatosis - very rare disease of the lymphatic vessels by Král, Zdeněk, Krejčí, Marta, Červinková, Ivana, Pour, Luděk, Štork, Martin, Krejčí, Martin, Sandecká, Viera, Adam, Zdeněk

“…Lymphangiomatosis is rare disease, we can find this entity in differential diagnosis of osteolytic leasions of bones of unknown origin. Typical sign for…”
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Therapy of 3 patients with Erdhiem-Chester disease with cladribin or cladribin in combination with cyclophosphamide. Case report and review of the therapy by Král, Zdeněk, Řehák, Zdeněk, Krejčí, Marta, Koukalová, Renata, Ševčíková, Sabina, Pour, Luděk, Krejčí, Martin, Štork, Martin, Sandecká, Viera, Adam, Zdeněk

“…Three adult patients with confirmed Erdheim-Chester disease (ECD) are followed at our department. Cladribine in monotherapy or in combination with…”
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Assessment of the Blue Light Ocular Hazard by Solar Measurements and the Impact of Selected Sunglasses Based upon the Limits of the International Commission on Non-Ionizing Radiation Protection Guideline by Krejci, Martin, Caruso, Giuseppe

“…A quantitative assessment of the blue light hazard for the human eye related to direct solar irradiation is presented. For six radiation situations, missing…”
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Multicentric Castlemans disease. Symptoms, diagnostics and therapy by Adam, Zdeněk, Řehák, Zdeněk, Adamová, Zuzana, Koukalová, Renata, Pour, Luděk, Krejčí, Marta, Boichuk, Ivanna, Sandecká, Viera, Krejčí, Martin, Štork, Martin, Ševčíková, Sabina, Král, Zdeněk

“…Castleman disease (CD) describes a group of heterogeneous hematologic disorders with characteristic histopathological features. CD can present with unicentric…”
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Transformation of IgM-MGUS into Waldenström´s macroglobulinemia in two of six patients treated for Schnitzler´s syndrome by Adam, Zdeněk, Tomíška, Miroslav, Řehák, Zdeněk, Koukalová, Renata, Krejčí, Marta, Král, Zdeněk, Adamová, Zuzana, Ševčíková, Sabina, Pour, Luděk, Štork, Martin, Krejčí, Martin, Sandecká, Viera

“…Transformation of IgM-MGUS into Waldenström´s macroglobulinemia in two of six patients treated for Schnitzler´s syndrome Schnitzler´s syndrome is a very rare,…”
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Langerhans cell histiocytosis (LCH). Overview of symptoms of LCH, which may lead the patients to any of these medical specialists by Adam, Zdeněk, Pour, Luděk, Tomíška, Miroslav, Starý, Karel, Horváth, Teodor, Doubková, Martina, Nebeský, Tomáš, Řehák, Zdeněk, Koukalová, Renata, Krejčí, Marta, Krejčí, Martin, Boichuk, Ivanna, Štork, Martin, Ševčíková, Sabina, Adamová, Zuzana, Král, Zdeněk

“…Langerhans cell histiocytosis (LCH) is a rare condition with incidence in adults 1-2/1 million, wherein Langerhans cells proliferate abnormally, adversely…”
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Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations by Adam, Zdeněk, Brančiková, Dagmar, Romanová, Gabriela, Pour, Luděk, Krejčí, Marta, König, Jiří, Nebeský, Tomáš, Adamová, Zuzana, Štork, Martin, Krejčí, Martin, Ševčíková, Sabina, Eid, Michal, Král, Zdeněk

“…Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu syndrome, is an autosomal dominant disorder that causes abnormal blood vessel…”
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Unicentric Castlemans disease. Symptoms, diagnostics and therapy by Adam, Zdeněk, Řehák, Zdeněk, Adamová, Zuzana, Koukalová, Renata, Pour, Luděk, Krejčí, Marta, Boichuk, Ivanna, Krejčí, Martin, Štork, Martin, Ševčíková, Sabina, Král, Zdeněk

“…Castleman disease (CD) includes a group of rare and heterogeneous disorders with characteristic lymph node histopathological abnormalities. CD can occur in a…”
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Complete remission of necrobiotic xanthogranuloma after disappearance of monoclonal immunoglobulin induced by bortezomib, lenalidomid and dexamethasone by Adam, Zdeněk, Pour, Luděk, Řehák, Zdeněk, Dvořáková, Klára, Koukalová, Renata, Feit, Josef, Kameník, Petr, Krejčí, Marta, Štork, Martin, Krejčí, Martin, Sandecká, Viera, Boichuk, Ivanna, Král, Zdeněk

“…Necrobiotic xanthogranuloma (NXG) is a rare chronic condition, belonging to the group non-Langerhans cell histiocytoses, which is relevant due to the…”
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Hereditary hemorrhagic telangiectasia (OslerWeberRendu syndrome) - Part II. Pharmacological therapy and international guidelines for the therapy 2020 by Adam, Zdeněk, Brančiková, Dagmar, Romanová, Gabriela, Pour, Luděk, Krejčí, Marta, König, Jiří, Nebeský, Tomáš, Adamová, Zuzana, Štork, Martin, Krejčí, Martin, Ševčíková, Sabina, Eid, Michal, Sandecká, Viera, Král, Zdeněk

“…Hereditary hemorrhagic telangiectasia also known as Osler-Weber-Rendu syndrome, is an disorder that causes abnormal blood vessel formation with bleeding…”
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Factors that influence the success of small and medium enterprises in ICT: a case study from the Czech Republic by Čábelková, Inna, Krejčí, Martin, Strielkowski, Wadim

“…Small and medium enterprises (SMEs) occupy a large niche in the information and technology sector (ICT) and play an important role in the functioning on any…”
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Outcome of COVID-19 infection in 50 multiple myeloma patients treated with novel drugs: single-center experience by Krejci, Marta, Pour, Ludek, Adam, Zdenek, Sandecka, Viera, Stork, Martin, Sevcikova, Sabina, Krejci, Martin, Knechtova, Zdenka, Kral, Zdenek

“…Infections are the primary cause of morbidity and mortality in multiple myeloma (MM) patients (pts). The aim of our retrospective analysis was to evaluate…”
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Brightness Scaling of High Power Laser Diode Bars by Manz, Yvonne M., Krejci, Martin, Weiss, Stefan, Thies, Achim, Schulz, Daniel, Fily, Arnaud, Lichtenstein, Norbert

“…High power laser diode bars used in pumping units of solid state or fibre lasers or as a direct source in laser diode systems have in the last years become…”
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