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Hemolytic anemia
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publication
Hyperbilirubinemia as manifestation of hemolytic anemia due to inborn defect of pyruvate kinase
2007 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Microangiopathic Hemolytic Anemia and Thrombocytopenia (cr-TTP) in a Patient with Generalized Gastric Adenocarcinoma
2003 |
First Faculty of Medicine
publication
Ulcerative colitis and development of the hemolytic anemia
2000 |
Publication without faculty affiliation
publication
TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins
2022 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Mathematics and Physics
publication
Hyperbilirubinemia as manifestation of hemolytic anemia due to inborn defect of pyruvate kinase
2007 |
Central Library of Charles University, Faculty of Medicine in Pilsen
publication
Lung diseases and autoimmune hemolytic anemia associted with IgG4 disease
2020 |
Third Faculty of Medicine
publication
Microangiopathic Hemolytic Anemia and Thrombocytopenia (cr-TTP) in a Patient with Generalized Gastric Adenocarcinoma
2003 |
Faculty of Medicine in Hradec Králové
publication
Fludarabine-induced autoimmune hemolytic anemia in a CLL patient: rituximab as the treatment of choice?
2007 |
Faculty of Medicine in Hradec Králové
publication
Fludarabine - induced autoimmune hemolytic anemia in a CLL patient : Rituximab as the treatmen of choice
Publication without faculty affiliation
publication
Pyruvate kinase deficiency in children
2012 |
Publication without faculty affiliation
publication
Herpesviridae. A Young Man with Acute Liver Failure and Hemolysis
2023 |
Faculty of Medicine in Pilsen
publication
New autoimmune diseases after cord blood transplantation: a retrospective study of EUROCORD and the Autoimmune Disease Working Party of the European Group for Blood and Marrow Transplantation
2013 |
Second Faculty of Medicine
publication
Molecular characterization of six new cases of red blood cell hexokinase deficiency yields four novel mutations in HK1
2016 |
Faculty of Medicine in Hradec Králové
publication
Secondary autoimmune diseases occurring after HSCT for an autoimmune disease: a retrospective study of the EBMT Autoimmune Disease Working Party
2011 |
Faculty of Physical Education and Sport
publication
A man with painless jaundice, anaemia and intermittent chest pain - case report
2015 |
Faculty of Medicine in Pilsen
publication
Evans' syndrome in a child with diabetes mellitus
1998 |
Second Faculty of Medicine
publication
The Treatment of anemia - 2nd Part
2007 |
First Faculty of Medicine
publication
Sharon Moalem: Health killing. Why we need disease
2009 |
First Faculty of Medicine
publication
Hydrops fetalis and failure of hematopoietic stem cell transplantation - A long route to the diagnosis of SPTA1-associated hereditary spherocytosis
2022 |
Second Faculty of Medicine, Central Library of Charles University
publication
Fatal case of diarrhea-associated hemolytic uremic syndrome with severe neurologic involvement
2012 |
Second Faculty of Medicine, Central Library of Charles University
publication
Hemolytic-uremic syndrome by children
2020 |
Second Faculty of Medicine
publication
Eculizumab treatment of child with hemolytic-uremic syndrome associated with Escherichia coli infection - case report
2020 |
Second Faculty of Medicine
publication
Severe secondary immune thrombocytopenia in a patient with chronic lymphocytic leukemia
2022 |
Faculty of Medicine in Hradec Králové, Faculty of Pharmacy in Hradec Králové
publication
Caplacizumab in the tratment of the thrombotic thrombocytopenic purpura - case report
2022 |
Faculty of Medicine in Hradec Králové
publication
Thrombotic microangiopathies - hemolytic-uremic syndromes and thrombotic thrombocytopenic purpura
2017 |
Second Faculty of Medicine
publication
Relevance of the autoantibodies detection in patients on immunoglobulin replacement therapy
2022 |
First Faculty of Medicine, Second Faculty of Medicine
publication
High Prevalence of Likely Passively Acquired Anti-TPO and Anti-GAD Autoantibodies in Common Variable Immunodeficiency
2022 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Hemolytic uremic syndrome (hus) - one of the most common causes of acute renal failure in childhood. complexity of the pathophysiology and novel diagnostic and therapeutic options for atypical forms
2010 |
Second Faculty of Medicine
publication
Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP
2012 |
Second Faculty of Medicine
publication
Rhesus-minus phenotype as a predictor of sexual desire and behavior, wellbeing, mental health, and fecundity
2020 |
Faculty of Science