Filters
Hereditary movement disorders genetic variability of parkinsonian and hyperkinetic syndromes (NW24-04-00067)
Hereditary movement disorders: genetic variability of parkinsonian and hyperkinetic syndromes The incidence of neurodegenerative diseases is increasing with the growing population, increasing average life expectancy and improving a...
Human genetics
- 2024 - 2027 •
- 16 593 tis. Kč •
- 16 593 tis. Kč •
- MZ
Řešení projektu: 1. 5. 2024 - 31. 12. 2027
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
Clinical and molecular-biological correlates of attention deficit hyperactivity disorder in children (NF6520)
To continue in the present results of molecular-genetic studies of ADHD in children and to make multi-branch study to identify and evaluate the relation of molecular-genetic results with psychological and psychiatrical finds. To verify the hypothesis...
FL - Psychiatrie, sexuologie
- 2001 - 2005 •
- 4 368 tis. Kč •
- 4 259 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2001 - 1. 1. 2005
Uznané náklady
Podpora ze státního rozpočtu (98%)
Poskytovatel: Ministerstvo zdravotnictví
Risk factors in persistent form of hyperkinetic disorder(ADHD) .Longitudinal, clinic and molecular-genetic study. (NR9298)
Annotation: Further to the results of the project IGA MZ CR 6520-5 of the years 2000-2005, the variants of ADHD course will be monitored within a longitudinal study in 100 boys which had an exactly diagnosed subtype of the disorder in childhood and t...
FL - Psychiatrie, sexuologie
- 2007 - 2009 •
- 2 716 tis. Kč •
- 2 716 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2007 - 31. 12. 2009
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
Submicroscopic chromosomal deletions - genotype-phenotype relation and a longitudinal study of patients (NE6912)
significant microdeletion syndromes, longitudinal follow up of phenotype changes syndromes for medical specialists who can see patients and families with microdeletion syndromes. Characterisation and specification of criti...
FG - Pediatrie
- 2002 - 2005 •
- 3 306 tis. Kč •
- 3 207 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2002 - 1. 1. 2005
Uznané náklady
Podpora ze státního rozpočtu (97%)
Poskytovatel: Ministerstvo zdravotnictví
Prediction of changes in parameters of metabolic syndrome X related to changes of betahydroxybutate as a marker of ketegenesis in a study with physical activity at patients with metabolic syndrome X (NR8384)
The aim of this study is prediction of changes in parameters of metabolic syndrome X in study with physical activity in metabolic patients. Quantifications of relations between some parameters of metabolic syndrome X and their chang...
FB - Endokrinologie, diabetologie, metabolismus, výživa
- 2005 - 2007 •
- 3 626 tis. Kč •
- 3 588 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2005 - 31. 12. 2007
Uznané náklady
Podpora ze státního rozpočtu (99%)
Poskytovatel: Ministerstvo zdravotnictví
Molecular diagnosis of Bartter and Gitelman syndrome (NR8116)
We will specify the prevalence of Bartter and Gitelman syndrome in Czech Republic, establish DNA diagnosis to differentiate and diagnose the variants. The obtained data will also help in more understanding of the pathogenesis of arterial hyp...
EB - Genetika a molekulární biologie
- 2004 - 2006 •
- 2 564 tis. Kč •
- 2 556 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2004 - 1. 1. 2006
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
Burn-out syndrom at Assessment physicians, its causes and solutions (ZVZ 200) (HR175/08)
Analyse of high-risk factor of burn-out syndrom Concept of sultions...
AQ - Bezpečnost a ochrana zdraví, člověk – stroj
- 2008 - 2008 •
- 295 tis. Kč •
- 295 tis. Kč •
- MPSV
Řešení projektu: 9. 9. 2008 - 30. 11. 2008
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo práce a sociálních věcí
Prevention of gonadal tumors in patients with Turner syndrome. (NE5892)
Demonstration of Y chromosome material usually results in prophylactic gonadectomy.DNA analysis in Turner syndrome patients focused on detection of chromosome Y cryptic sequences in mosaic representation. Improvement of the clinical manageme...
FG - Pediatrie
- 2000 - 2002 •
- 1 755 tis. Kč •
- 1 755 tis. Kč •
- MZ
Řešení projektu: 1. 1. 2000 - 1. 1. 2002
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
Biology and immunopathology of bone marrow failure and combined autoimmune cytopenia (Evans syndrome) in children (NV18-07-00430)
Bone marrow failure is rare in childhood. Following disorders are planned to be studied: aplastic anemia, myelodysplastic syndrome and combined immune cytopenias (Evans syndrome). Immunological mechanisms play role in the pathogenes...
Oncology
- 2018 - 2021 •
- 10 854 tis. Kč •
- 10 854 tis. Kč •
- MZ
Řešení projektu: 1. 5. 2018 - 31. 12. 2021
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
Systematic review focusing on Diuretics and nephrotic syndrome (NS9936)
The aim of our project is (in cooperation with The Renal Cochrane Group) creation of a systematic review on topic: Diuretics in the treatment of nephrotic syndrome.......
FR - Farmakologie a lékárnická chemie
- 2008 - 2011 •
- 727 tis. Kč •
- 727 tis. Kč •
- MZ
Řešení projektu: 1. 7. 2008 - 31. 12. 2011
Uznané náklady
Podpora ze státního rozpočtu (100%)
Poskytovatel: Ministerstvo zdravotnictví
- 1 - 10 out of 566