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MUDr. Veronika Krulišová Ph.D.
External person at Second Faculty of Medicine
12 publications
Publications
publication
Analytical parameters and validation of homopolymer detection in a pyrosequencing-based next generation sequencing system
2018 |
Second Faculty of Medicine
publication
Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study
2017 |
Second Faculty of Medicine, Faculty of Pharmacy in Hradec Králové
publication
A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening
2016 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Results of expanded newborn screening in the Czech Republic
2014 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations
2014 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Distribution of CFTR mutations in the Czech population: Positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations
2013 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
publication
Prospective and parallel assessments of cystic fibrosis newborn screening protocols in the Czech Republic: IRT/DNA/IRT versus IRT/PAP and IRT/PAP/DNA
2012 |
Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
publication
Current Diagnostic Strategies and Overview of Preimplantation, Prenatal and Postnatal DNA Diagnostics of Cystic Fibrosis in the Czech Republic
2008 |
Second Faculty of Medicine, Third Faculty of Medicine
publication
Under the mask of Kabuki syndrome: Elucidation of genetic-and phenotypic heterogeneity in patients with Kabuki-like phenotype
2018 |
Second Faculty of Medicine
publication
Complex morphological and molecular genetic examination of amelogenesis imperfecta: A case presentation of two Czech siblings with a non-syndrome form of the disease
2014 |
Second Faculty of Medicine
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