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Hyperglycaemia
Person
Class
Person
Publication
Programmes
doc. MUDr. Štěpánka Průhová Ph.D.
Academic staff at Second Faculty of Medicine
6 classes
199 publications
Classes
class
Summer holidays training I
D0108104 |
Second Faculty of Medicine
class
Summer holidays training II
D0108107 |
Second Faculty of Medicine
class
Summer holidays training III
D0110106 |
Second Faculty of Medicine
class
Summer holidays training IV
D0110107 |
Second Faculty of Medicine
class
Clinical 10 days
+1
D0110K10 |
Second Faculty of Medicine
Publications
publication
Maturity-onset diabetes of the young 3 (MODY 3)
2006 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Intravenous Glucose Tolerance Test in Differential Diagnosis of Randomly Found Hyperglycaemia in Children and Adolescents
2005 |
Third Faculty of Medicine
publication
Hyperglycaemia in Children and Adolescents: Diagnostic Approach
2003 |
Third Faculty of Medicine
publication
Differential diagnosis of hyperglycaemia in children and young adults
2003 |
Third Faculty of Medicine
publication
Persistent mild hyperglycaemia in several family members: discovery of a novel mutation Glu268Stop in the glucokinase gene (MODY 2)
2002 |
Third Faculty of Medicine
publication
Glycemic control by treatment modalities: national registry-based population data in children and adolescents with type 1 diabetes
2024 |
Faculty of Mathematics and Physics, Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Introduction of continuous glucose monitoring (CGM) is a key factor in decreasing HbA1c in war refugee children with type 1 diabetes
2024 |
Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine, Central Library of Charles University
publication
The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)
2024 |
Second Faculty of Medicine
publication
Integrative role of the SALL4 gene: From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary
2024 |
Second Faculty of Medicine
publication
SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary
2024 |
Second Faculty of Medicine
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