UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

High incidence of candidaemia in a nationwide cohort: Underlying diseases, risk factors and mortality

International journal of infectious diseases, 2018-11, Vol.76, p.58-63

2018

Volltextzugriff (PDF)

100 Microbial physiology and persistence of Pseudomonas aeruginosa airway infections

Journal of cystic fibrosis, 2017-06, Vol.16, p.S90-S90

2017

Volltextzugriff (PDF)

Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis

Journal of cystic fibrosis, 2013-12, Vol.12 (6), p.638-643

2013

Volltextzugriff (PDF)

Achromobacter species in cystic fibrosis: Cross-infection caused by indirect patient-to-patient contact

Journal of cystic fibrosis, 2013-12, Vol.12 (6), p.609-615

2013

Volltextzugriff (PDF)

Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis

Journal of cystic fibrosis, 2011-09, Vol.10 (5), p.318-325

2011

Volltextzugriff (PDF)

127 Collateral sensitivity cycling of antibiotics for cystic fibrosis airway infections

Journal of cystic fibrosis, 2016-06, Vol.15, p.S83-S83

2016

Volltextzugriff (PDF)

Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients

Journal of cystic fibrosis, 2009-01, Vol.8 (1), p.58-62

2009

Volltextzugriff (PDF)

P196 Establishment of a co-culture air-liquid-interphase lung model utilizing human macrophages

Journal of cystic fibrosis, 2024-06, Vol.23, p.S115-S116

2024

Volltextzugriff (PDF)

WS19.6 Diversity of Pseudomonas aeruginosa in cystic fibrosis airways

Journal of cystic fibrosis, 2015-06, Vol.14, p.S36-S36

2015

Volltextzugriff (PDF)

80 Persistence of Pseudomonas aeruginosa in early stages of airway infection

Journal of cystic fibrosis, 2016-06, Vol.15, p.S71-S72

2016

Volltextzugriff (PDF)

53 Genome changes leading to persistence of Pseudomonas aeruginosa in the airways of CF patients

Journal of cystic fibrosis, 2014-06, Vol.13, p.S60-S60

2014

Volltextzugriff (PDF)

WS21.1 The genetic basis of Pseudomonas aeruginosa pathoadaptation to the airways of cystic fibrosis patients

Journal of cystic fibrosis, 2014-06, Vol.13, p.S41-S41

2014

Volltextzugriff (PDF)

WS16.3 Rethinking Pseudomonas aeruginosa (PA) lung infection: using molecular microbiology rather than culture and antibodies

Journal of cystic fibrosis, 2014-06, Vol.13, p.S33-S33

2014

Volltextzugriff (PDF)

116 Pharmacokinetic variability of ciprofloxacin in cystic fibrosis – is CYP3A4 involved?

Journal of cystic fibrosis, 2015-06, Vol.14, p.S86-S86

2015

Volltextzugriff (PDF)

76 Sinus surgery postpones chronic Gram-negative lung infection: cohort study of 106 patients with cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S70-S71

2016

Volltextzugriff (PDF)

EPS9.04 Lung epithelial 3D air-liquid-interface culture systems for high-resolution investigations of bacterial infection dynamics during treatment with elexacaftor/tezacaftor/ivacaftor (ETI)

Journal of cystic fibrosis, 2024-06, Vol.23, p.S61-S61

2024

Volltextzugriff (PDF)

Pharmacokinetic variability of clarithromycin and differences in CYP3A4 activity in patients with cystic fibrosis

Journal of cystic fibrosis, 2014-03, Vol.13 (2), p.179-185

2014

Volltextzugriff (PDF)

55 Investigation of the RetS–GacAS regulatory network in clinical Pseudomonas aeruginosa isolates reveals evolutionary adaptation

Journal of cystic fibrosis, 2014-06, Vol.13, p.S60-S60

2014

Volltextzugriff (PDF)

353 Achromobacter xylosoxidans in cystic fibrosis: indirect patient-to-patient contact can lead to cross-infection

Journal of cystic fibrosis, 2012-06, Vol.11, p.S147-S147

2012

Volltextzugriff (PDF)

WS24.2 Extensive sinus surgery and follow-up can eradicate pathogenic bacterial sinusitis in patients with cystic fibrosis (CF)

Journal of cystic fibrosis, 2012-06, Vol.11, p.S53-S53

2012

Volltextzugriff (PDF)

WS14.04 Pseudomonas aeruginosa infection drives complex host responses in a cystic fibrosis-derived airway model

Journal of cystic fibrosis, 2023-06, Vol.22, p.S29-S29

2023

Volltextzugriff (PDF)

P141 Microbiological evaluation of an automated UV-disinfection robot on cystic fibrosis-related pathogens

Journal of cystic fibrosis, 2023-06, Vol.22, p.S107-S107

2023

Volltextzugriff (PDF)

WS1.1 Evolutionary pathways in two dominant clinical Pseudomonas aeruginosa clones

Journal of cystic fibrosis, 2013-06, Vol.12, p.S1-S1

2013

Volltextzugriff (PDF)

151 Sino-pulmonary pairs of mucoid and non-mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients with chronic airways infection have similar gene expression profiles

Journal of cystic fibrosis, 2011-06, Vol.10, p.S38-S38

2011

Volltextzugriff (PDF)

P209 Mucus composition and interactions with Pseudomonas aeruginosa in chronically infected cystic fibrosis and primary ciliary dyskinesia patients

Journal of cystic fibrosis, 2024-06, Vol.23, p.S133-S133

2024

Volltextzugriff (PDF)

1 – 25 von 71

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(70)
Mit Volltextzugriff
(68)

Publikationsform

Artikel
(70)
Buchkapitel
(1)

Sprache

Englisch
(71)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

High incidence of candidaemia in a nationwide cohort: Underlying diseases, risk factors and mortality

100 Microbial physiology and persistence of Pseudomonas aeruginosa airway infections

Early treatment with inhaled antibiotics postpones next occurrence of Achromobacter in cystic fibrosis

Achromobacter species in cystic fibrosis: Cross-infection caused by indirect patient-to-patient contact

Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis

127 Collateral sensitivity cycling of antibiotics for cystic fibrosis airway infections

Long-term, low-dose azithromycin treatment reduces the incidence but increases macrolide resistance in Staphylococcus aureus in Danish CF patients

P196 Establishment of a co-culture air-liquid-interphase lung model utilizing human macrophages

WS19.6 Diversity of Pseudomonas aeruginosa in cystic fibrosis airways

80 Persistence of Pseudomonas aeruginosa in early stages of airway infection

53 Genome changes leading to persistence of Pseudomonas aeruginosa in the airways of CF patients

WS21.1 The genetic basis of Pseudomonas aeruginosa pathoadaptation to the airways of cystic fibrosis patients

WS16.3 Rethinking Pseudomonas aeruginosa (PA) lung infection: using molecular microbiology rather than culture and antibodies

116 Pharmacokinetic variability of ciprofloxacin in cystic fibrosis – is CYP3A4 involved?

76 Sinus surgery postpones chronic Gram-negative lung infection: cohort study of 106 patients with cystic fibrosis

EPS9.04 Lung epithelial 3D air-liquid-interface culture systems for high-resolution investigations of bacterial infection dynamics during treatment with elexacaftor/tezacaftor/ivacaftor (ETI)

Pharmacokinetic variability of clarithromycin and differences in CYP3A4 activity in patients with cystic fibrosis

55 Investigation of the RetS–GacAS regulatory network in clinical Pseudomonas aeruginosa isolates reveals evolutionary adaptation

353 Achromobacter xylosoxidans in cystic fibrosis: indirect patient-to-patient contact can lead to cross-infection

WS24.2 Extensive sinus surgery and follow-up can eradicate pathogenic bacterial sinusitis in patients with cystic fibrosis (CF)

WS14.04 Pseudomonas aeruginosa infection drives complex host responses in a cystic fibrosis-derived airway model

P141 Microbiological evaluation of an automated UV-disinfection robot on cystic fibrosis-related pathogens

WS1.1 Evolutionary pathways in two dominant clinical Pseudomonas aeruginosa clones

151 Sino-pulmonary pairs of mucoid and non-mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients with chronic airways infection have similar gene expression profiles

P209 Mucus composition and interactions with Pseudomonas aeruginosa in chronically infected cystic fibrosis and primary ciliary dyskinesia patients

Suchergebnisse filtern