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autosomal dominant polycystic kidney disease
Person
Class
Person
Publication
Programmes
Věra Kebrdlová
Person without affiliation with CUNI
59 publications
Publications
publication
New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease
2009 |
First Faculty of Medicine
publication
The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy
2007 |
First Faculty of Medicine
publication
Molecular genetic analysis in families with autosomal dominant polycystic kidney disease
Publication without faculty affiliation
publication
DNA analysis of autosomal dominant polycystic kidney disease in Czech families
+1
Publication without faculty affiliation
publication
Mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease in Czech Republic (1)
Publication without faculty affiliation
publication
Mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease in Czech Republic
Publication without faculty affiliation
publication
Detection of SHOX gene aberrations in routine diagnostic practice and evaluation of phenotype scoring form effectiveness
2017 |
First Faculty of Medicine
publication
Analysis of common SHOX gene sequence variants and similar to 4.9-kb PAR1 deletion in ISS patients
+1
2014 |
Faculty of Science, First Faculty of Medicine
publication
Application of the new insertion-deletion polymorphism kit for forensic identification and parentage testing on the Czech population
2013 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families
2013 |
First Faculty of Medicine
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