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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease cystic fibrosis
Symptom C0009450|infection
Sentences 124
PubMedID- 21545738 M. abscessus infection was associated with cystic fibrosis and m. xenopi infection was associated with male gender.
PubMedID- 21494150 Purpose of review: lung disease in cystic fibrosis (cf) results from chronic airway infection and inflammation leading to progressive bronchiectasis and respiratory failure.
PubMedID- 24925006 Eradication strategy for persistent methicillin-resistant staphylococcus aureus infection in individuals with cystic fibrosis--the pmep trial: study protocol for a randomized controlled trial.
PubMedID- 20097812 The ubiquitous opportunistic human pathogen pseudomonas aeruginosa secretes a viscous extracellular polysaccharide, called alginate, as a virulence factor during chronic infection of patients with cystic fibrosis.
PubMedID- 20729233 Background: initial pulmonary pseudomonas aeruginosa infection in patients with cystic fibrosis (cf) is currently treated with intensive antibiotic therapy.
PubMedID- 20019078 During the chronic lung infection of patients with cystic fibrosis (cf), pseudomonas aeruginosa can survive for long periods due to adaptive evolution mediated by genetic variation.
PubMedID- 21893650 Comparative efficacy and safety of 4 randomized regimens to treat early pseudomonas aeruginosa infection in children with cystic fibrosis.
PubMedID- 20211000 Nocardia farcinica lung infection in a patient with cystic fibrosis: a case report.
PubMedID- 22916223 Defective mucus secretion may result in failure of host defense against pathogens, which in turn could be the underlying pathogenesis of airway infection in patients with cystic fibrosis (cf) 2.
PubMedID- 22708424 Results: survival medians for 1991-2000 and 2001-2010 was 25.7 and 35.1 years, respectively in the group of mucoviscidosis patients with staphylococcus aureus infection survival was significantly higher than in those infected with gram-negative microflora.
PubMedID- 22785192 The genus achromobacter currently is comprised of seven species, including achromobacter xylosoxidans, an opportunistic and nosocomial pathogen that displays broad-spectrum antimicrobial resistance and is recognized as causing chronic respiratory tract infection in persons with cystic fibrosis (cf).
PubMedID- 20218338 Identification of possible mechanisms of lung infection in patients with cystic fibrosis will allow to develop evidence-based system of prevention of infectious complications in these patients.
PubMedID- 21067323 Previously considered to have minimal inherent virulence owing to their commensal ability, the last decade has heralded an increasing recognition of candida infection among patients with cystic fibrosis.
PubMedID- 25709717 Similarly, emond and co-workers chose samples for exome sequencing based on the extremes of the first time to pseudomonas infection in individuals with cystic fibrosis.
PubMedID- 22081229 The identification of 17 b. dolosa genes that underwent selective pressure during infection in subjects with cystic fibrosis highlights key pathways involved in pathogenesis and may suggest new therapeutic targets for this and other lung infections.
PubMedID- 20238363 Neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis.
PubMedID- 25815200 2010 dabigatranprevention of stroke or systemic embolism in patients with non-valvular atrial fibrillationboehringer ingelheim pty ltdpbsfinancially-basedpublic summary document atomoxetine hydrochlorideadhd diagnosed between the ages of 6 and 18 yearseli lilly australia pty ltdpbsfinancially-basedpublic summary document fingolimodrrmsnovartis pharmaceuticals australia pty ltdpbsfinancially-based; outcome-basedpublic summary document cinacalcet hydrochlorideend stage renal disease receiving dialysis who have uncontrolled secondary hyperparathyroidismamgen australia pty ltdpbsfinancially-basedpbs schedule , public summary document clostridium botulinum type a toxin-haemagglutinin complexsevere spasticity of the upper limb in adults following a stroke, as an adjunct to physical therapyipsen pty ltdpbsfinancially-basedpublic summary document fentanyl citratefentanyl lozenges for the treatment of breakthrough painorphan australia pty ltdpbsfinancially-basedpublic summary document natalizumabrrmsbiogen idec australia pty ltdpbsfinancially-basedpublic summary document paliperidoneschizophreniajanssen-cilag pty ltdpbsfinancially-basedpublic summary document botulinum toxin type a purified neurotoxin complexmoderate to severe spasticity of the upper limb in adults following a stroke as an adjunct to physical therapyallergan australia pty ltdpbsfinancially-basedpublic summary document tenofovir disoproxil fumaratetreatment of chronic hepatitis bgilead sciences pty ltdpbsfinancially-basedpublic summary document pramipexole hydrochlorideidiopathic parkinson diseaseboehringer ingelheim pty ltdpbsfinancially-basedpublic summary document tobramycinpseudomonas aeruginosa respiratory infection in a patient with cystic fibrosisnovartis pharmaceuticals australia pty ltdpbsfinancially-basedpublic summary document ticagreloracs, mi, or unstable anginaastrazeneca pty ltdpbsfinancially-basedpublic summary document pregabalinneuropathic painpfizer australia pty ltdpbsfinancially-basedpublic summary document rivaroxabanacute symptomatic dvtbayer australia ltdpbsfinancially-basedpublic summary document aztreonampseudomonas aeruginosa infection in patients with cystic fibrosisgilead sciences pty ltdpbsfinancially-basedpublic summary document crinone (progesterone gel)supplement progesterone in women who have luteal phase defectmerck seronopbsfinancially-basedrobertson et al.
PubMedID- 25705428 In the last decade, many studies published the use of colistin in the treatment of lung infection in patients without cystic fibrosis, with conflicting results.
PubMedID- 24091166 Background: inhaled tobramycin therapy has been shown to be efficacious in clinical trials for the eradication of initial pseudomonas aeruginosa infection in children with cystic fibrosis (cf).
PubMedID- 23375733 Prevalence of helicobacter pylori infection in patients with cystic fibrosis.
PubMedID- 25027419 Rationale: pseudomonas aeruginosa (pa) serology could potentially be a useful adjunct to respiratory culture methods for the detection of initial or early pa infection in patients with cystic fibrosis (cf).
PubMedID- 23984384 However, the most serious medical problem caused by p. aeruginosa is lung infection associated with cystic fibrosis 3.
PubMedID- 24696136 However, the role of antibiotic treatment of stenotrophomonas maltophilia infection in people with cystic fibrosis is still unclear.
PubMedID- 22336832 Palivizumab for prophylaxis against respiratory syncytial virus infection in children with cystic fibrosis.
PubMedID- 25470304 Antibiotic treatment for nontuberculous mycobacteria lung infection in people with cystic fibrosis.
PubMedID- 20678316 We report an outbreak of corynebacterium pseudodiphtheriticum infection in children with cystic fibrosis (cf).
PubMedID- 22940004 There is clear evidence some viral infections are associated with cystic fibrosis that dual infection is more likely to produce symptoms, and mechanisms of viral-induced exacerbation should be elucidated.
PubMedID- 20185551 A coordinated approach has been used to measure the fitness of bcc bacteria isolated from cystic fibrosis (cf) patients with chronic bcc infection using methods relevant to bcc growth and survival conditions.
PubMedID- 20146956 Nocardia farcinica infection in a patient with cystic fibrosis.
PubMedID- 22762867 Comparison of two treatment regimens for eradication of pseudomonas aeruginosa infection in children with cystic fibrosis.
PubMedID- 22592739 However, the role of antibiotic treatment of stenotrophomonas maltophilia infection in people with cystic fibrosis is still unclear.
PubMedID- 20942647 Aeruginosa cell counts in a rat lung infection model and in patients with cystic fibrosis.
PubMedID- 24510624 Colistimethate sodium dry powder for inhalation: a review of its use in the treatment of chronic pseudomonas aeruginosa infection in patients with cystic fibrosis.
PubMedID- 23737087 Palivizumab for prophylaxis against respiratory syncytial virus infection in children with cystic fibrosis.
PubMedID- 24515341 Objectives: to assess the effects of neuraminidase inhibitors for the treatment of influenza infection in people with cystic fibrosis.
PubMedID- 23066486 Emergence of pseudomonas aeruginosa cross-infection in children with cystic fibrosis attending an iranian referral pediatric center.
PubMedID- 25146522 Aeruginosa infection in patients with cystic fibrosis.
PubMedID- 24851825 Palivizumab for prophylaxis against respiratory syncytial virus infection in children with cystic fibrosis.
PubMedID- 22717532 Objective: to examine the incidence of recurrent clostridium difficile infection in patients with cystic fibrosis (cf), including patients who had undergone lung transplantation, and review clinical findings in hospitalized patients with c.
PubMedID- 20166098 Palivizumab for prophylaxis against respiratory syncytial virus infection in children with cystic fibrosis.
PubMedID- 26003071 Aeruginosa in order to evaluate the epidemiological situation of this infection in patients with cystic fibrosis attending our centre; 2.
PubMedID- 24064077 Bacterial sinusitis can be a focus for initial lung colonisation and chronic lung infection in patients with cystic fibrosis.
PubMedID- 20951086 Murine models of acute and chronic lung infection with cystic fibrosis pathogens.
PubMedID- 25068317 Pseudomonas aeruginosa can grow to very high-cell-density (hcd) during infection of the cystic fibrosis (cf) lung.
PubMedID- 22119262 Aims: to know the characteristics and prevalence of non-tuberculous mycobacterial infection infection in patients with non-cystic fibrosis bronchiectasis.
PubMedID- 25741986 Selection criteria: randomized controlled trials of antibiotic therapy based on biofilm antimicrobial susceptibility testing compared to antibiotic therapy based on conventional antimicrobial susceptibility testing in the treatment of pseudomonas aeruginosa pulmonary infection in people with cystic fibrosis.
PubMedID- 21189901 Results reveal that they have a potential role as a novel antimicrobial agent for the treatment of infection due to cystic fibrosis (cf)-related opportunistic pathogens.
PubMedID- 24648553 Trichosporon mycotoxinivorans infection in patients with cystic fibrosis.
PubMedID- 25241695 Human rhinovirus infection in children with cystic fibrosis.
PubMedID- 22905192 It is a leading cause of acute pneumonia in hospitalized patients and is responsible for chronic lung infection in patients with cystic fibrosis.

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