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Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials

Journal of cystic fibrosis, 2011-06, Vol.10, p.S79-S81

2011

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Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report

Journal of cystic fibrosis, 2011-06, Vol.10, p.S75-S78

2011

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Cystic fibrosis in the Czech Republic

Journal of cystic fibrosis, 2008-06, Vol.7, p.S114-S114

Vavrova, V

2008

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WS5.5 Economic burden of cystic fibrosis (CF): prevalence based cost of illness analysis related to the lung disease severity in Czech CF patients

Journal of cystic fibrosis, 2014-06, Vol.13, p.S11-S11

2014

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179 Lung transplantation in cystic fibrosis: waiting list results

Journal of cystic fibrosis, 2012-06, Vol.11, p.S102-S102

2012

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Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Journal of medical genetics, 2004-08, Vol.41 (8), p.629-633

2004

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Genetic variants of transferrin in cystic fibrosis

Journal of inherited metabolic disease, 2008-06, Vol.31 (3), p.457-461

2008

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228 Cepacia syndrome caused by Burkholderia cenocepacia ST-32 strain: risk factors

Journal of cystic fibrosis, 2011, Vol.10, p.S58-S58

2011

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Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin

Journal of clinical pharmacy and therapeutics, 2008-08, Vol.33 (4), p.409-417

2008

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Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Thorax, 2005-04, Vol.60 (4), p.320-325

2005

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Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin

Journal of clinical pharmacy and therapeutics, 2008-08, Vol.33 (4), p.409-417

2008

Volltextzugriff (PDF)

Effect of early physiotherapy intervention in CF babies persists at least till 12 years of age

Journal of cystic fibrosis, 2010, Vol.9, p.S75-S75

2010

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137 The end of a long-term outbreak with highly transmissible Burkholderia cenocepacia ST32

Journal of cystic fibrosis, 2011, Vol.10, p.S35-S35

2011

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Forty years isolation from W. Europe and its influence on the course of CF: an unwanted experiment

Journal of cystic fibrosis, 2008-06, Vol.7, p.S114-S114

2008

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Cystic fibrosis-related diabetes (CFRD) in the Czech Republic

Journal of cystic fibrosis, 2008-06, Vol.7, p.S84-S84

2008

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19 Summary of the simultaneous IRT/PAP/ST+DNA and IRT/DNA/IRT newborn screening protocols in the Czech Republic

Journal of cystic fibrosis, 2011, Vol.10, p.S5-S5

2011

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ECORN-CF project in the Czech Republic: first experiences

Journal of cystic fibrosis, 2008-06, Vol.7, p.S118-S118

2008

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Is intestinal inflammation present in CF patients?

Journal of cystic fibrosis, 2008-06, Vol.7, p.S80-S80

2008

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Factors influencing the worsening of lung function between 16 and 18 years of age in Czech patients

Journal of cystic fibrosis, 2009, Vol.8, p.S59-S59

2009

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Genetic modifiers of liver disease in cystic fibrosis

JAMA : the journal of the American Medical Association, 2009-09, Vol.302 (10), p.1076

2009

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Hypoglycosylation and disease modifying polymorphism in cystic fibrosis

Journal of cystic fibrosis, 2008-06, Vol.7, p.S3-S3

2008

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Manual contact-stimulating physiotherapy: a very important part of chest physiotherapy in CF infants

Journal of cystic fibrosis, 2008-06, Vol.7, p.S74-S74

2008

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Clinical outcome and CF care costs justify the need of newborn screening

Journal of cystic fibrosis, 2008-06, Vol.7, p.S14-S14

2008

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Spectrum of CFTR mutations in the Czech Republic

Journal of cystic fibrosis, 2010, Vol.9, p.S2-S2

2010

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POSSIBILITIES AND PROBLEMS OF USING PUPILLARY REFLEX FOR SUBCONSCIOUS DETECTION OF CONSUMER PREFERENCES

Metalurgija, 2014-01, Vol.53 (1), p.85-88

2014

Volltextzugriff (PDF)

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Pulmonary exacerbation: Towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials

Chronic Pseudomonas aeruginosa infection definition: EuroCareCF Working Group report

Cystic fibrosis in the Czech Republic

WS5.5 Economic burden of cystic fibrosis (CF): prevalence based cost of illness analysis related to the lung disease severity in Czech CF patients

179 Lung transplantation in cystic fibrosis: waiting list results

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Genetic variants of transferrin in cystic fibrosis

228 Cepacia syndrome caused by Burkholderia cenocepacia ST-32 strain: risk factors

Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Serum cystatin C level for better assessment of glomerular filtration rate in cystic fibrosis patients treated by amikacin

Effect of early physiotherapy intervention in CF babies persists at least till 12 years of age

137 The end of a long-term outbreak with highly transmissible Burkholderia cenocepacia ST32

Forty years isolation from W. Europe and its influence on the course of CF: an unwanted experiment

Cystic fibrosis-related diabetes (CFRD) in the Czech Republic

19 Summary of the simultaneous IRT/PAP/ST+DNA and IRT/DNA/IRT newborn screening protocols in the Czech Republic

ECORN-CF project in the Czech Republic: first experiences

Is intestinal inflammation present in CF patients?

Factors influencing the worsening of lung function between 16 and 18 years of age in Czech patients

Genetic modifiers of liver disease in cystic fibrosis

Hypoglycosylation and disease modifying polymorphism in cystic fibrosis

Manual contact-stimulating physiotherapy: a very important part of chest physiotherapy in CF infants

Clinical outcome and CF care costs justify the need of newborn screening

Spectrum of CFTR mutations in the Czech Republic

POSSIBILITIES AND PROBLEMS OF USING PUPILLARY REFLEX FOR SUBCONSCIOUS DETECTION OF CONSUMER PREFERENCES

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