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adenosine deaminase
Person
Class
Person
Publication
Programmes
MUDr. Ivan Šebesta CSc.
Academic staff at First Faculty of Medicine
9 classes
91 publications
Classes
class
Biochemistry 1 D
B00178 |
First Faculty of Medicine
class
Biochemistry 2 D
B00530 |
First Faculty of Medicine
class
Renovating business
B01599 |
First Faculty of Medicine
class
Blood sampling technique
B01607 |
First Faculty of Medicine
class
Case studies from laboratory diagnostics
B02089 |
First Faculty of Medicine
class
Clinical biochemistry 1
B02568 |
First Faculty of Medicine
class
Clinical biochemistry 2
B02588 |
First Faculty of Medicine
class
Inovating Business
B81599 |
First Faculty of Medicine
class
Blood Sampling Techniques
B81607 |
First Faculty of Medicine
Publications
publication
Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia
2022 |
First Faculty of Medicine
publication
Modified forearm ischemic test in hypouricemic patients
2020 |
First Faculty of Medicine
publication
Hereditary xanthinuria is not so rare disorder of purine metabolism
2018 |
First Faculty of Medicine
publication
Hypouricemia and hyperuricosuria in a pubescent girl: Questions & Answers
2018 |
First Faculty of Medicine
publication
Clinical Biochemistry
2016 |
First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen, Faculty of Mathematics and Physics, Central Library of Charles University, Second Faculty of Medicine
publication
Genetic background of uric acid metabolism in a patient with severe chronic tophaceous gout
2016 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2
2016 |
First Faculty of Medicine, Faculty of Science
publication
Purine disorders with hypouricemia
2014 |
First Faculty of Medicine
publication
Purine and pyrimidine disorders
2014 |
First Faculty of Medicine
publication
Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis
2013 |
First Faculty of Medicine, Third Faculty of Medicine, Faculty of Science
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