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doc. MUDr. Felix Votava Ph.D.
Academic staff at Third Faculty of Medicine
14 classes
67 publications
Classes
class
Pediatrics, gynecology and obstetrics
+1
C4VL008 |
Third Faculty of Medicine
class
Paediatrics - I.
C5VL005 |
Third Faculty of Medicine
class
Peadiatrics II.
+1
C6VL001 |
Third Faculty of Medicine
class
ERASMUS - Practice - Paediatrics
CERA0P0022 |
Third Faculty of Medicine
class
ERASMUS - Pediatrics, gynecology and obstetrics - summer
CERA4P0051 |
Third Faculty of Medicine
class
ERASMUS - Pediatrics, gynecology and obstetrics - winter
CERA4P0055 |
Third Faculty of Medicine
class
ERASMUS - Paediatrics - I.
CERA5P0081 |
Third Faculty of Medicine
class
ERASMUS - Module of Paediatrics - Peadiatrics II.
CERA6P0056 |
Third Faculty of Medicine
class
Clinical Medicine Basics V. - Pediatrics, Gerontology
CNT053P3 |
Third Faculty of Medicine
class
Module of Paediatrics - Paediatrics - I.
CPADXX35 |
Third Faculty of Medicine
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Publications
publication
Two novel fusion genes, AIF1L-ETV6 and ABL1-AIF1L, result together with ETV6-ABL1 from a single chromosomal rearrangement in acute lymphoblastic leukemia with prenatal origin
2018 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Macro AST - cause of asymptomatic aspartate aminotransferase elevation - case report
2018 |
Third Faculty of Medicine, First Faculty of Medicine
publication
ACTH dependent Cushing's syndrome - case report
2018 |
Third Faculty of Medicine
publication
Acute Leukemias with ETV6/ABL1 (TEL/ABL) Fusion: Poor Prognosis and Prenatal Origin
2010 |
Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine
publication
Neonatal screening in the Czech Republic
2010 |
Third Faculty of Medicine, First Faculty of Medicine
publication
Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency
2009 |
Third Faculty of Medicine
publication
anamnézy; defekt jednoho genu
2006 |
Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Central Library of Charles University, Faculty of Physical Education and Sport
publication
Differential diagnosis of polyuria and polydipsia
2001 |
Third Faculty of Medicine
publication
Newborn screening-detected 21-hydroxylase deficiency: growth pattern is not associated with the genotype
2024 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Diferenciální diagnostika polyurie-polydipsie
2024 |
Third Faculty of Medicine
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