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563 (0,172s) •

Project

Diagnosis and detection of mutations in the COL4A5 gene in patients with Alpot syndrome. (IZ3783)

FG - Pediatrie

  • 1996 - 1998
    • •
  • 1 830 tis. Kč
    • •
  • 1 829 tis. Kč
    • •
  • MZ
Project

Identification and characterization of genetic factors contributing to inherited tubulointerstitial kidney disease II (NU21-07-00033)

kidney disease and Alport syndrome. We established an international registry of >1000Autosomal dominant tubuloinsterstitial kidney diseases (ADTKD) refers to a clinical syndrome characterized by autosomal dominant inherita...

Human genetics

  • 2021 - 2024
    • •
  • 12 754 tis. Kč
    • •
  • 12 754 tis. Kč
    • •
  • MZ
Project

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
Project

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
Project

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
Project

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
Project

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
Project

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
Project

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
Project

Epidemiologic monitoring of screening for Down´s syndrome. (IZ3197)

FG - Pediatrie

  • 1995 - 1997
    • •
  • 203 tis. Kč
    • •
  • 193 tis. Kč
    • •
  • MZ
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