The chest roentgenogram in cystic fibrosis: a new scoring system.
about
Pulmonary outcome prediction (POP) tools for cystic fibrosis patients.Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileusClinical and microbiological features of Inquilinus sp. isolates from five patients with cystic fibrosis.Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.Modified Chrispin-Norman chest radiography score for cystic fibrosis: observer agreement and correlation with lung function.Growth and pulmonary outcomes during the first 2 y of life of breastfed and formula-fed infants diagnosed with cystic fibrosis through the Wisconsin Routine Newborn Screening ProgramManagement of refractory Pseudomonas aeruginosa infection in cystic fibrosisShwachman-Kulczycki score still useful to monitor cystic fibrosis severityPharmacokinetics of vancomycin in adult cystic fibrosis patients.Chest computed tomography scores of severity are associated with future lung disease progression in children with cystic fibrosis.The Novel CFTR Mutation A457P in a Male with a Delayed Diagnosis of Cystic FibrosisPharmacokinetics and dosage requirements of netilmicin in cystic fibrosis patients.The sensitivity of lung disease surrogates in detecting chest CT abnormalities in children with cystic fibrosis.Is limited computed tomography the future for imaging the lungs of children with cystic fibrosis?Computed tomography in children with cystic fibrosis: a new way to reduce radiation dose.A High Level of Soluble CD40L Is Associated with P. aeruginosa Infection in Patients with Cystic FibrosisCritical evaluation of three chest radiograph scores in cystic fibrosisAssessment of hyperinflation in children with cystic fibrosisPersistence mechanisms in Pseudomonas aeruginosa from cystic fibrosis patients undergoing ciprofloxacin therapy.Pseudomonas aeruginosa variants isolated from patients with cystic fibrosis are killed by a bactericidal protein from human polymorphonuclear leukocytes.Sepsis Caused by Achromobacter Xylosoxidans in a Child with Cystic Fibrosis and Severe Lung Disease.Association of lung function, chest radiographs and clinical features in infants with cystic fibrosisRadiography, tomosynthesis, CT and MRI in the evaluation of pulmonary cystic fibrosis: an untangling review of the multitude of scoring systems.Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis.Risk factors for the progression of cystic fibrosis lung disease throughout childhood.Novel end points for clinical trials in young children with cystic fibrosisChest radiology in cystic fibrosis: is scoring useful?Pulmonary exacerbations and clinical outcomes in a longitudinal cohort of infants and preschool children with cystic fibrosis.Early life growth patterns persist for 12 years and impact pulmonary outcomes in cystic fibrosis.
P2860
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P2860
The chest roentgenogram in cystic fibrosis: a new scoring system.
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
The chest roentgenogram in cystic fibrosis: a new scoring system.
@en
type
label
The chest roentgenogram in cystic fibrosis: a new scoring system.
@en
prefLabel
The chest roentgenogram in cystic fibrosis: a new scoring system.
@en
P2093
P1433
P1476
The chest roentgenogram in cystic fibrosis: a new scoring system.
@en
P2093
P407
P577
1979-01-01T00:00:00Z