V. Skalická

发表

Low-dose insulin therapy in patients with cystic fibrosis and early-stage insulinopenia prevents deterioration of lung function: a 3-year prospective study

Z. Šumník, J. Lebl, D. Zemková, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Selective Increase in Blood Dendritic Cell Antigen‐3‐Positive Dendritic Cells in Bronchoalveolar Lavage Fluid in Allergic Patients

A. Šedivá, J. Kopecká, R. Spíšek, 2012, Scandinavian journal of immunology.

Serum α-Glutathione S-Transferase as a Sensitive Marker of Hepatocellular Damage in Patients with Cystic Fibrosis

V. Vávrová, M. Pechová, M. Chada, 2003 .

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, K. De Boeck, 2009, Thorax.

Political stringency, infection rates, and higher education students' adherence to government measures in the Nordic countries and the UK during the first wave of the COVID-19 outbreak

A. Quickfall, S. M. Van de Velde, G. Berg-Beckhoff, 2022, Preventive Medicine.

Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study

J. Klimeš, M. Macek, M. Turnovec, 2015, The European Journal of Health Economics.

The impact of chest computed tomography and chest radiography on clinical management of cystic fibrosis lung disease.

C. Hansen, H. Tiddens, V. Raia, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Prospective and parallel assessments of cystic fibrosis newborn screening protocols in the Czech Republic: IRT/DNA/IRT versus IRT/PAP and IRT/PAP/DNA

M. Macek, Miroslava Balaščáková, T. Piskáčková, 2012, European Journal of Pediatrics.

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.

M. Macek, M. Turnovec, Miroslava Balaščáková, 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nitrogen multiple breath washout test for infants with cystic fibrosis

P. Pohunek, V. Skalická, V. Koucký, 2018, European Respiratory Journal.

Ag Complexes of NHC Ligands Bearing Polyfluoroalkyl and/or Polyfluoropolyalkoxy Ponytails. Why Are Polyethers More Fluorous Than Alkyls?

J. Cvačka, M. Kvíčalová, A. Březinová, 2012 .

Polyfluoroalkylated tripyrazolylmethane ligands: Synthesis and complexes

J. Cvačka, M. Kvíčalová, A. Březinová, 2011 .

A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening.

O. Sommerburg, M. Macek, J. Hammermann, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Epidemiology of rare diseases detected by newborn screening in the Czech Republic.

M. Macek, R. Gaillyová, T. Adam, 2019, Central European journal of public health.

Serum alpha-glutathione S-transferase as a sensitive marker of hepatocellular damage in patients with cystic fibrosis.

R. Průša, K. Kotaška, V. Vávrová, 2003, Physiological research.

Physicochemical and biopharmaceutical characterization of novel Matrix-Liposomes.

H. Kauczor, D. Witzigmann, G. Fricker, 2020, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

Comparison of different IRT-PAP protocols to screen newborns for cystic fibrosis in three central European populations.

M. Muckenthaler, M. Gahr, O. Sommerburg, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Investigation of Structure-Activity Relationships of Dexrazoxane Analogs Reveals Topoisomerase IIβ Interaction as a Prerequisite for Effective Protection against Anthracycline Cardiotoxicity

M. Štěrba, J. Kubeš, M. Adamcová, 2020, The Journal of Pharmacology and Experimental Therapeutics.

Skin wipe test: A simple, inexpensive, and fast approach in the diagnosis of cystic fibrosis

P. Dřevínek, M. Dastych, F. Foret, 2020, Pediatric pulmonology.

Mutations in the amiloride‐sensitive epithelial sodium channel in patients with cystic fibrosis‐like disease

P. Lebecque, A. Azad, M. Schwartz, 2009, Human mutation.

Clinically Translatable Prevention of Anthracycline Cardiotoxicity by Dexrazoxane Is Mediated by Topoisomerase II Beta and Not Metal Chelation

A. Lyon, M. Štěrba, J. Kubeš, 2021, Circulation. Heart failure.

Pilot newborn screening project for cystic fibrosis in the Czech Republic: defining role of the delay in its symptomatic diagnosis and influence of ultrasound-based prenatal diagnosis on the incidence of the disease.

M. Macek, P. Dřevínek, Miroslava Balaščáková, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

PCR detection of Burkholderia cepacia complex as one of key factors to handle a long-term outbreak.

P. Dřevínek, O. Cinek, O. Melter, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.

Milan Macek, Gérard Lenoir, J. Sarles, 2010, American journal of respiratory and critical care medicine.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, I. Sermet, 2009, Thorax.