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Pyruvate kinase
Person
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Person
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Zdeňka Černá
External person at Faculty of Medicine in Pilsen
39 publications
Publications
publication
Hyperbilirubinemia as manifestation of hemolytic anemia due to inborn defect of pyruvate kinase
2007 |
Faculty of Medicine in Pilsen, Central Library of Charles University
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
Consensual guidelines of the Czech National Haemophilia Programme (CNHP) for the diagnosis and treatment of patients with haemophilia, 3rd edition, year 2021
2021 |
Faculty of Medicine in Pilsen, Second Faculty of Medicine
publication
Consensual guidelines of the Czech National Haemophilia Programme (CNHP) for the diagnosis and treatment of patients with congenital haemophilia and FVIII/ FIX inhibitors
2021 |
Faculty of Medicine in Pilsen, Second Faculty of Medicine
publication
An uncommon cause of splenomegaly
2021 |
Faculty of Medicine in Pilsen
publication
Consensual guidelines of the Czech National Haemophilia Programme (CNHP) for replacement treatment of patients with haemophilia during invasive procedures and surgery, 2nd edition, year 2020
2020 |
Faculty of Medicine in Pilsen, Second Faculty of Medicine
publication
What do cats bring?
2019 |
Faculty of Medicine in Pilsen
publication
Autoimmune disease, familial clustering and thyroid carcinoma coexistent with autoimmune thyroiditis in children and adolescence: A cross-sectional study from the Czech Republic
2018 |
Faculty of Medicine in Pilsen
publication
Czech Working Group for Paediatric Gastroenterology and Nutrition guidelines for diagnostics and treatment of inflammatory bowel diseases in children - 1st edition update
2017 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G
2017 |
Faculty of Medicine in Pilsen
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