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hnf4a
Publication
Class
Person
Publication
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publication
How can genetic investigation contribute to choice of proper treatment of diabetic patient
2010 |
Second Faculty of Medicine
publication
De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed
2014 |
Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
publication
The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes
2016 |
Second Faculty of Medicine
publication
A novel-192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetes
2006 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
Lack of PAX4 mutations in 53 Czech MODYX families
2010 |
Second Faculty of Medicine
publication
Half-Life of Sulfonylureas in HNF1A and HNF4A Human MODY Patients is not Prolonged as Suggested by the Mouse Hnf1a(-/-) Model
2015 |
Third Faculty of Medicine
publication
Association of birthweight and penetrance of diabetes in individuals with HNF4A-MODY: a cohort study
2022 |
Second Faculty of Medicine
publication
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young
2008 |
Second Faculty of Medicine
publication
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes
+1
2011 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
Hepatocyte nuclear factors and diabetes mellitus
2017 |
Third Faculty of Medicine
publication
Congenital hyperinsulinism: Loss of B-cell self-control
2016 |
Second Faculty of Medicine
publication
MODY in Ukraine: genes, clinical phenotypes and treatment
2017 |
Second Faculty of Medicine
publication
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
2019 |
First Faculty of Medicine
publication
Hypoglycemia and antihyperglycemic treatment in adult MODY patients - A systematic review of literature
2019 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents
2006 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism
2015 |
Third Faculty of Medicine, Second Faculty of Medicine, First Faculty of Medicine
publication
Three novel mutations in MODY and its phenotype in three different Czech families
2010 |
Faculty of Medicine in Pilsen, Third Faculty of Medicine
publication
The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia
2015 |
Second Faculty of Medicine
publication
Expression Profiling of Nme7 Interactome in Experimental Models of Metabolic Syndrome
2018 |
First Faculty of Medicine
publication
Autoantibodies against ZnT8 are rare in Central-European LADA patients and absent in MODY patients, including those positive for other autoantibodies
2019 |
Third Faculty of Medicine
publication
Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme
2016 |
Second Faculty of Medicine
publication
Hidden MODY-Looking for a Needle in a Haystack
2018 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
Heterogeneity of gestational diabetes - Do we take MODY into consideration as much as we should?
2019 |
Third Faculty of Medicine, Second Faculty of Medicine