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Jana Bartošová
Observed names:
J Bartosová,
J Bartošová,
J. Bartosova,
J. Bartošová,
Jana Bartosova,
Jana Bartošová
show all 6
Observed institutions:
Poznan University of Medical Sciences,
Centre Hospitalier de Luxembourg,
Charles University,
Universidad de Buenos Aires,
University Hospital Galway,
University Hospital in Motol,
Cardiff University
show all 7
OpenAlex ID:
A5065595084
Polymorphisms of TGF-beta1 in cystic fibrosis patients
2006
·
Jitka Brazova
, Kristyna Sismova
, et al.
·
Clinical Immunology
·
52
Low-dose insulin therapy in patients with cystic fibrosis and early-stage insulinopenia prevents deterioration of lung function: a 3-year prospective study
2011
·
Stanislava Koloušková
, Daniela Zemková
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
51
Widespread clone of Burkholderia cenocepacia in cystic fibrosis patients in the Czech Republic
2005
·
Pavel Drevinek
, Sarka Vosahlikova
, et al.
·
Journal of Medical Microbiology
·
39
Evaluation of TD test for analysis of persistence or tolerance in clinical isolates of Staphylococcus aureus
2019
·
Hana Kotková
, Marie Cabrnochová
, et al.
·
Journal of Microbiological Methods
·
28
Direct PCR Detection of Burkholderia cepacia Complex and Identification of Its Genomovars by Using Sputum as Source of DNA
2002
·
Pavel Dřevínek
, Hana Hrbáčková
, et al.
·
Journal of Clinical Microbiology
·
28
Antineutrophil cytoplasmic antibodies directed against bactericidal/permeability-increasing protein detected in children with cystic fibrosis inhibit neutrophil-mediated killing of Pseudomonas aeruginosa
2003
·
Anna Šedivá
, Jiřina Bartůňková
, et al.
·
Microbes and Infection
·
24
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
2012
·
Petra Křenková
, Tereza Piskáčková
, et al.
·
Journal of Cystic Fibrosis
·
21
PDF
Serum alpha-glutathione S-transferase as a sensitive marker of hepatocellular damage in patients with cystic fibrosis
2003
·
K Šídlová
, V Skalická
, et al.
·
Physiological Research
·
20
PDF
Insulin-like growth factor-I and insulin-like growth factor-binding protein-3 in cystic fibrosis: a positive effect of antibiotic therapy and hyperalimentation
2001
·
J Lebl
, M Zahradníková
, et al.
·
Acta Paediatrica
·
20
PCR detection of Burkholderia cepacia complex as one of key factors to handle a long-term outbreak
2012
·
Klara Dedeckova
, Libor Fila
, et al.
·
Journal of Cystic Fibrosis
·
19
PDF
[Cystic fibrosis--a disease of adolescents and adults?].
1999
·
V Vávrová
, D Zemková
, et al.
·
PubMed
·
2
P060 Impact of elexacaftor/tezacaftor/ivacaftor on eradication of nontuberculous mycobacteria in children with cystic fibrosis: case series from Czech Republic
2024
·
M. Kreslová
, V. Skalická
, et al.
·
Journal of Cystic Fibrosis
·
1
Novorozenecký screening cystické fibrózy a diagnostika CFSPID.
2019
·
Jana Bartošová
, D. Zemková
, et al.
·
1
Forty years isolation from W. Europe and its influence on the course of CF: an unwanted experiment
2008
·
D. Zemkova
, V. Skalicka
, et al.
·
Journal of Cystic Fibrosis
·
1
PDF
Lung transplantation for cystic fibrosis: immune system and autoimmunity.
2001
·
A Sedivá
, R Lischke
, et al.
·
PubMed
·
1
CFTR function in airway epithelial cells derived from CFSPID/CRMS individuals
2026
·
L. Borek Dohalska
, T. Dousova
, et al.
·
Journal of Cystic Fibrosis
Complex CFTR alleles harbouring two cystic fibrosis–causing variants, including E831X
2026
·
A. Holubová
, M. Libik
, et al.
·
Journal of Cystic Fibrosis
Unexpected finding in the airways of a child with cystic fibrosis
2026
·
Anna Šmejkalová
, Václav Koucký
, et al.
·
Pediatrie pro praxi
Pica‐Induced Airway Obstruction in Paediatric Cystic Fibrosis: An Unexpected Culprit
2025
·
Anna Šmejkalová
, Václav Koucký
, et al.
·
Pediatric Pulmonology
297 Evaluation of CFTR function in airway epithelial cells from CF-SPID individuals
2025
·
L. Borek-Dohalska
, S. Novotna
, et al.
·
Journal of Cystic Fibrosis
Lung function tracking and its determinants in cystic fibrosis from infancy to preschool age.
2025
·
Radim Bláha
, Tereza Holeček-Krištofová
, et al.
·
European Respiratory Journal
P035 Generally positive clinical outcomes of CFSPID cases identified between 2009 and 2023 within the nationwide neonatal screening programme in the Czech Republic
2025
·
J. Bartošová
, A. Holubová
, et al.
·
Journal of Cystic Fibrosis
The relationship between infant and preschool lung function in cystic fibrosis. A pilot follow-up study.
2024
·
Václav Koucký
, Radim Bláha
, et al.
·
European Respiratory Journal
855 Efficacy of elexacaftor/tezacaftor/ivacaftor in nontuberculous mycobacterial eradication in children with CF: a nationwide observation from the Czech Republic
2024
·
M. Kreslová
, V. Skalická
, et al.
·
Journal of Cystic Fibrosis
P029 Complex CFTR allele F508del-L467F in the era of elexacaftor/tezacaftor/ivacaftor (ETI) therapy: a retrospective analysis in three Czech cases who partially respond to ETI
2024
·
M. Kreslová
, M. Libik
, et al.
·
Journal of Cystic Fibrosis
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Works count:
46
Citation count:
308
H-index:
10
I10-index:
10
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