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Cystic Fibrosis
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Your search returned 36 results
from the time period: last 90 days.
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American journal of respiratory and critical care medicine
AbstractText: The severity of cystic fibrosis (CF) lung disease varies widely, even for Phe508del homozygotes. Heritability studies show that >50% of the variability reflects non-CFTR genetic variation; however the full extent of the pertinent genetic variation is not known AbstractText: We sought to identify novel CF disease-modifying mechanisms using an integrated approach based on analyzing "in vivo" CF ...
Lung Diseases (5), Cystic Fibrosis (2), Infections (1), more mentions
The European respiratory journal
Modelling future trends in cystic fibrosis demography using the French Cystic Fibrosis Registry: update and sensitivity analysis..
Cystic Fibrosis (4), more mentions
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
Liver transplantation in adult cystic fibrosis: Clinical, imaging and pathological evidence of obliterative portal venopathy..
Cystic Fibrosis (2), more mentions
American journal of respiratory and critical care medicine
The Respective Roles of LCI and MRI in the Clinical Management of Cystic Fibrosis Patients..
Cystic Fibrosis (2), more mentions
American journal of respiratory and critical care medicine
X Chromosome Encoded MicroRNAs are Functionally Increased in Cystic Fibrosis Monocytes..
Cystic Fibrosis (2), more mentions
Journal of clinical anesthesia
Massive hemoptysis during general endotracheal anesthesia in adults with Cystic Fibrosis..
Cystic Fibrosis (2), Hemoptysis (2), more mentions
International journal of antimicrobial agents
The first Spanish multi-centre study on the microbiology of cystic fibrosis (CF) was conducted from 2013 to 2014. The study involved 24 CF units from 17 hospitals, and recruited 341 patients. The aim of this study was to characterise Pseudomonas aeruginosa isolates, 79 of which were recovered from 75 (22%) patients.
Infectious Diseases (2)
Cystic Fibrosis (2), more mentions
The European respiratory journal
Mycobacterium abscessus in patients with cystic fibrosis: low impact of inter-human transmission in Italy..
Cystic Fibrosis (2), more mentions
American journal of respiratory and critical care medicine
Early Intervention of Cystic Fibrosis Pulmonary Exacerbations Based on Home Monitoring - "eICE Through the Looking Glass"..
Cystic Fibrosis (2), more mentions
10. Expanded Cystic Fibrosis Therapy.  
Date: 07/03/2017
JAMA
Expanded Cystic Fibrosis Therapy..
Cystic Fibrosis (2), more mentions
American journal of rhinology & allergy
AbstractText: A correlation exists between the microbial flora of the upper and lower airways in patients with cystic fibrosis (CF) or with primary ciliary dyskinesia (PCD. The sinuses can function as a bacterial reservoir where gram-negative bacteria adapt to the airways and repeatedly are aspirated to and colonize the lungs according to the theory of the united (unified) airways.
Kartagener Syndrome (3), Cystic Fibrosis (2), Human Influenza (1), more mentions
FEMS microbiology letters 
Abstract: Pseudomonas aeruginosa is a major pathogen in the lungs of cystic fibrosis (CF) patients... Keyword: cystic fibrosis. Keyword: interspecific interactions: multispecies interactions. Keyword: microbial communities. Keyword: microbiome.
Cystic Fibrosis (3), more mentions
PloS one
Abstract: Cystic Fibrosis is an autosomal recessive disorder caused by mutations in the CFTR gene... Here, we describe a high efficiency strategy for editing of three different rare CFTR mutations which together account for about 3% of individuals with Cystic Fibrosis. The mutations cause aberrant splicing of CFTR mRNA due to the creation of cryptic splice signals that result in ...
Cystic Fibrosis (3), more mentions
Current opinion in pulmonary medicine
AbstractText: In cystic fibrosis (CF) patients with end-stage pulmonary disease, lung transplantation (LTx) remains a life-extending therapy with good outcome in most patients. Despite early concern about chronic pretransplantation infections in the context of posttransplantation immunosuppression, typical CF-associated organisms such as Pseudomonas aeruginosa turned out to be quite well manageable and associated with favorable outcomes in transplanted ...
Cystic Fibrosis (2), Infections (2), Lung Diseases (1), more mentions
PloS one
Abstract: Cystic Fibrosis (CF) is the most common monogenic disease among people of Western European descent and caused by mutations in the CFTR gene. However, the disease severity is immensely variable even among patients with similar CFTR mutations due to the possible effect of 'modifier genes'. To identify genetic modifiers, we applied RNA-seq based transcriptomic analyses in CF patients ...
Cystic Fibrosis (2), more mentions
Thorax
Abstract: While Pseudomonas aeruginosa (PA) cross-infection is well documented among patients with cystic fibrosis (CF), the equivalent risk among patients with non-CF bronchiectasis (NCFB) is unclear, particularly those managed alongside patients with CF... Keyword: cystic Fibrosis. Keyword: infection control. Keyword: respiratory infection.
Infections (4), Cystic Fibrosis (3), Bronchiectasis (3), more mentions
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
Abstract: Burkholderia sp. infections are extremely complex in cystic fibrosis (CF) patients, especially considering the lack of knowledge regarding its behavior, its relationship with prognosis, as well as its transmissibility and multidrug resistance features. This study evaluated the frequency of chronic infection by Burkholderia, using microbiological and clinical data. Ninety-eight patients with CF attended from July 2011 to April ...
Infectious Diseases (3), Anti-Obesity and Weight Loss (2)
Infections (5), Cystic Fibrosis (2), more mentions
The Annals of thoracic surgery
The purpose of this study was to determine whether PRD impacts survival after LT in patients with cystic fibrosis (CF) AbstractText: We queried the United Network for Organ Sharing (UNOS) database to identify all adult (≥18 years) recipients with CF who underwent isolated LT from May 4, 2005 to December ...
Cystic Fibrosis (2), more mentions
Proceedings of the National Academy of Sciences of the United States of America
Accordingly, we developed a mathematical model to describe the dynamic coupling of ion and water transport to extracellular purinergic signaling. We trained our model from steady-state and time-dependent experimental measurements made using normal and cystic fibrosis (CF) cultured human airway epithelium... Keyword: cystic fibrosis. Keyword: mathematical modeling. Keyword: purinergic signaling.
Cystic Fibrosis (3), Lung Diseases (1), more mentions
Current opinion in pulmonary medicine
AbstractText: Methicillin-resistant Staphylococcus aureus (MRSA) remains prevalent in people with cystic fibrosis (CF. As chronic infection with worse pulmonary outcomes develops frequently, the organism is concerning to CF providers and patients. This review describes current epidemiology, our understanding of risk factors for MRSA infection, and relevant aspects of treatment with review of new and ongoing trials AbstractText: Prevalence ranges ...
Infectious Diseases (2), Endocrine Disorders (1)
Infections (3), Cystic Fibrosis (2), Exocrine Pancreatic Insufficiency (1), more mentions
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