Zobrazeno 1 - 10
of 36
pro vyhledávání: '"A. George F. Davidson"'
Publikováno v:
Journal of Pediatric Nursing. 30:236-243
The adequate preparation of cystic fibrosis (CF) youth for the transfer from pediatric to adult-based health care services is essential to meet the needs of this changing population. This paper describes the evolution of a transition clinic for patie
Publikováno v:
Current Opinion in Pulmonary Medicine. 18:615-621
Purpose of review This review is based upon the recent literature regarding eradication of newly acquired infection with Pseudomonas aeruginosa (Psa) in patients with cystic fibrosis (CF) and the economic and other effects of such an early eradicatio
Publikováno v:
Journal of Cystic Fibrosis. 10:175-180
Background Acquisition of Pseudomonas aeruginosa (Psa) and infection with mucoid strains is associated with repeated pulmonary exacerbations which often require intravenous and long-term nebulised antibiotic treatments, repeated hospitalizations and
Autor:
Eva Cho, Chanel Prestidge, Vanessa McMahon, A. George F. Davidson, Mark A. Chilvers, Colin T. White
Publikováno v:
Pediatric Nephrology. 26:605-612
With increasing life expectancy and the need for lung transplantation in the cystic fibrosis (CF) population, there are increasing reports of chronic kidney disease (CKD). However, values for baseline or longitudinal glomerular filtration rate (GFR)
Publikováno v:
Pediatric Pulmonology. 45:1064-1069
In N. America, over the past decade, various airway clearance techniques (ACT) have been introduced for the treatment of cystic fibrosis (CF). We hypothesized that autogenic drainage (AD), an ACT developed in Belgium would be as effective as postural
Publikováno v:
Environmental Toxicology and Pharmacology. 27:424-427
In metabolomic studies using liquid chromatography mass spectrometry of urine from children with cystic fibrosis (CF), high levels of metabolites of low molecular weight phthalates were found. Phthalate metabolite excretion was explained by therapy w
Publikováno v:
The American Journal of Clinical Nutrition. 81:686-691
BACKGROUND Hepatic steatosis and fat malabsorption are common in cystic fibrosis (CF). Choline deficiency results in decreased phosphatidylcholine synthesis through the cytidine diphosphocholine-choline pathway and hepatic steatosis and in increased
Autor:
Roger A. Dyer, A. George F. Davidson, Stepan Melnyk, Alice Chen, S. Jill James, Sheila M. Innis
Publikováno v:
The Journal of Pediatrics. 143:351-356
We used a novel approach based on the intersection of phospholipid and methionine metabolism at the S-adenosylmethionine (SAM)-dependent methylation of phosphatidylethanolamine (PE) to study potential alterations in phospholipid metabolism in childre
Autor:
David P. Speert, Lawrence T. K. Wong, Eshwar Mahenthiralingam, Ruth Milner, Fatma Taha, A. George F. Davidson, Anna M. Gravelle, M. E. Campbell, Deborah A. Henry
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 166:988-993
Pseudomonas aeruginosa is the most common respiratory pathogen in patients with cystic fibrosis (CF), but the predominant mechanism by which it is acquired is controversial. To determine the frequency of patient-to-patient spread, we evaluated P. aer
Autor:
Anna M. Gravelle, David P. Speert, M. E. Campbell, Pearce G. Wilcox, Lawrence T. K. Wong, Deborah A. Henry, A. George F. Davidson, Barbara E.M. Nakielna, Peter Vandamme, Eshwar Mahenthiralingam
Publikováno v:
Clinical Infectious Diseases. 33:1469-1475
Infection with Burkholderia cepacia complex in patients with cystic fibrosis (CF) results in highly variable\ud clinical outcomes. The purpose of this study was to determine if there are genomovar-specific disparities in\ud transmission and disease s