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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease cystic fibrosis
Symptom |infection
Sentences 124
PubMedID- 25830686 Maltophilia lung infection in patients with cystic fibrosis.
PubMedID- 23403223 Background: mycobacterium abscessus causes lung infection in patients with cystic fibrosis.
PubMedID- 22364820 Conclusion: genetic modifiers play a significant role in the establishment and timing of persistent pa infection in individuals with cystic fibrosis.
PubMedID- 22683550 P. aeruginosa is also responsible for pulmonary infection of patients with cystic fibrosis .
PubMedID- 24614401 We used antibiotic therapy of chronic lung infection in persons with cystic fibrosis as a model system to assess the influence of key variables of therapy on measures of microbial community perturbation.
PubMedID- 20503281 Pseudomonas aeruginosa (psa) is the most common pathogen to cause chronic lung infection in children with cystic fibrosis (cf), and is associated with an increase in both morbidity and mortality.
PubMedID- 20837573 Objectives: to test the presumption that pseudomonas aeruginosa isolates responsible for initial lung infection in individuals with cystic fibrosis (cf) are invariably susceptible to antipseudomonal agents.
PubMedID- 22396480 This is particularly true for the treatment of pseudomonas infection in patients with cystic fibrosis.
PubMedID- 26047157 Aeruginosa airway infection in persons with cystic fibrosis (cf; mim219700).
PubMedID- 20105324 Background: staphylococcus aureus infection in patients with cystic fibrosis (cf) is frequent and may be due to colonization by a few pathogenic lineages.
PubMedID- 25443661 Nocardia farcinica lung infection in a patient with cystic fibrosis and a lung transplant.
PubMedID- 26238926 Pulmonary mycobacterium abscessus sensu lato infection in patients without cystic fibrosis.
PubMedID- 21750293 Context: early pulmonary infection in children with cystic fibrosis leads to increased morbidity and mortality.
PubMedID- 25658563 Species of the burkholderia cepacia complex are associated with opportunistic infection in patients with cystic fibrosis.
PubMedID- 25027418 Pseudomonas aeruginosa infection is a hallmark of lung disease in cystic fibrosis.
PubMedID- 22401602 Challenges with current inhaled treatments for chronic pseudomonas aeruginosa infection in patients with cystic fibrosis.
PubMedID- 26517580 Neutrophil-associated inflammation during pseudomonas aeruginosa lung infection is a determinant of morbidity in cystic fibrosis (cf).
PubMedID- 24260360 A particularly serious medical problem caused by p. aeruginosa is chronic lung infection associated with cystic fibrosis .
PubMedID- 20950421 M. abscessus has been described as a prevalent ntm infection in children with cystic fibrosis 9.
PubMedID- 25657265 Pandoraea is an emerging respiratory pathogen capable of causing chronic lung infections in people with cystic fibrosis (cf), but the clinical significance of this infection is ambiguous.
PubMedID- 21310671 Anti-psa antibiotic therapy early in the course of psa infection in patients with cystic fibrosis (cf) may result in eradication of psa and prevention or delay of colonization with the organism.
PubMedID- 20098291 The risk of mold infection was higher in patients with cystic fibrosis (11%, 4 of 35) than other underlying lung diseases (4%, 10 of 269).
PubMedID- 24068273 Pseudomonas aeruginosa infection in patients with cystic fibrosis: scientific evidence regarding clinical impact, diagnosis, and treatment.
PubMedID- 23235684 Antibiotic treatment for nontuberculous mycobacteria lung infection in people with cystic fibrosis.

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