(Q28212180)

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Cystic fibrosis

scientific article (publication date: 22 February 2003)

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31 October 2019

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Cystic fibrosis (English)

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Europe PubMed Central

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31 October 2019

cystic fibrosis

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1

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31 October 2019

author name string

Gerd Döring

2

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1 February 2003

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31 October 2019

1 reference

Europe PubMed Central

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31 October 2019

361

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31 October 2019

681-689

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31 October 2019

9358

1 reference

Europe PubMed Central

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31 October 2019

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis: molecular biology and therapeutic implications

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The cystic fibrosis transmembrane conductance regulator: an intriguing protein with pleiotropic functions

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Correlation between genotype and phenotype in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The origin of the major cystic fibrosis mutation (delta F508) in European populations.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

HLA class II polymorphism in cystic fibrosis. A possible modifier of pulmonary phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Allotypes of alpha 1-antitrypsin in patients with cystic fibrosis, homozygous and heterozygous for deltaF508

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of alpha(1)-antichymotrypsin deficiency with milder lung disease in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

beta2 adrenoceptor gene polymorphisms in cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation by extracellular nucleotides of chloride secretion in the airway epithelia of patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The neglected ion: HCO3-

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Early alterations in airway mucociliary clearance and inflammation of the lamina propria in CF mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Inflammation and infection in naive human cystic fibrosis airway grafts

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Lower airway inflammation in infants and young children with cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Normal bronchial epithelial cells constitutively produce the anti-inflammatory cytokine interleukin-10, which is downregulated in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

IL-10 attenuates excessive inflammation in chronic Pseudomonas infection in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Transfer of a cathelicidin peptide antibiotic gene restores bacterial killing in a cystic fibrosis xenograft model

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Noninvasive in vivo fluorescence measurement of airway-surface liquid depth, salt concentration, and pH.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of reduced mucus oxygen concentration in airway Pseudomonas infections of cystic fibrosis patients

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mucoid conversion of Pseudomonas aeruginosa by hydrogen peroxide: a mechanism for virulence activation in the cystic fibrosis lung.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The cystic fibrosis gene and resting energy expenditure

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Diabetes mellitus in Danish cystic fibrosis patients: prevalence and late diabetic complications.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Insulin resistance with altered secretory kinetics and reduced proinsulin in cystic fibrosis patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Male fertility in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Water and electrolytes in cervical mucus from patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The diagnosis of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Making the diagnosis of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Ion transport abnormalities in rectal suction biopsies from children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Time to think again: cystic fibrosis is not an "all or none" disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Stool trypsin and chymotrypsin. Value in the diagnosis of pancreatic insufficiency in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Faecal elastase 1: a marker of exocrine pancreatic insufficiency in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

PARANASAL SINUSES IN CYSTIC FIBROSIS. INCIDENCE OF ROENTGEN ABNORMALITIES

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Nutritional benefits of neonatal screening for cystic fibrosis. Wisconsin Cystic Fibrosis Neonatal Screening Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Nutrition and survival in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Acquisition of Pseudomonas aeruginosa in children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene therapy in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Gentamicin in pharmacogenetic approach to treatment of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Limited proteolysis as a probe for arrested conformational maturation of delta F508 CFTR

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis F508del patients have apically localized CFTR in a reduced number of airway cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of deltaF508 CFTR in a cystic fibrosis respiratory epithelial cell line by 4-phenylbutyrate, genistein and CPX.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A pilot clinical trial of oral sodium 4-phenylbutyrate (Buphenyl) in deltaF508-homozygous cystic fibrosis patients: partial restoration of nasal epithelial CFTR function

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A phase I randomized, multicenter trial of CPX in adult subjects with mild cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cell-based assay for high-throughput quantitative screening of CFTR chloride transport agonists

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A pilot study of aerosolized amiloride for the treatment of lung disease in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The effect of topical benzamil and amiloride on nasal potential difference in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Safety of aerosolized INS 365 in patients with mild to moderate cystic fibrosis: results of a phase I multi-center study

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis. 1. Pseudomonas aeruginosa infection in cystic fibrosis and its management

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The changing epidemiology of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Antibiotic treatment of Staphylococcus aureus infection in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Persistent infection with small colony variant strains of Staphylococcus aureus in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prognosis in cystic fibrosis treated with continuous flucloxacillin from the neonatal period

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of continuous antistaphylococcal therapy on the rate of P. aeruginosa acquisition in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Antibiotic prophylaxis in infants and young children with cystic fibrosis: a randomized controlled trial

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

High frequency of hypermutable Pseudomonas aeruginosa in cystic fibrosis lung infection.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Adaptive resistance to tobramycin in Pseudomonas aeruginosa lung infection in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Improved survival in the Danish center-treated cystic fibrosis patients: results of aggressive treatment.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Elective versus symptomatic antibiotic treatment in cystic fibrosis patients with chronic Pseudomonas infection of the lungs

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term tobramycin aerosol therapy in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Colistin inhalation therapy in cystic fibrosis patients with chronic Pseudomonas aeruginosa lung infection

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Intermittent administration of inhaled tobramycin in patients with cystic fibrosis. Cystic Fibrosis Inhaled Tobramycin Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Improvement of survival in patients with diffuse panbronchiolitis treated with low-dose erythromycin

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term azithromycin may improve lung function in children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of long term treatment with azithromycin on disease parameters in cystic fibrosis: a randomised trial.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Long term azithromycin in children with cystic fibrosis: a randomised, placebo-controlled crossover trial

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Nebulised colomycin for early pseudomonas colonisation in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevention of chronic Pseudomonas aeruginosa colonisation in cystic fibrosis by early treatment

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment of Pseudomonas aeruginosa colonization in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of inhaled tobramycin on early Pseudomonas aeruginosa colonisation in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Alternate-day prednisone reduces morbidity and improves pulmonary function in cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A multicenter study of alternate-day prednisone therapy in patients with cystic fibrosis. Cystic Fibrosis Foundation Prednisone Trial Group

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of persistent growth impairment after alternate-day prednisone treatment in children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of high-dose ibuprofen in patients with cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Modulation of airway inflammation in cystic fibrosis. In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Pharmacokinetics of recombinant secretory leukoprotease inhibitor aerosolized to normals and individuals with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Aerosol α1 -antitrypsin treatment for cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Aerosolized prolastin suppresses bacterial proliferation in a model of chronic Pseudomonas aeruginosa lung infection

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A double-blind placebo controlled trial with oral ambroxol and N-acetylcysteine for mucolytic treatment in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparison of hypertonic saline and alternate-day or daily recombinant human deoxyribonuclease in children with cystic fibrosis: a randomised trial

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Survival effect of lung transplantation among patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Lung transplantation and life extension in children with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Lung transplantation for cystic fibrosis patients with Burkholderia cepacia complex. Survival linked to genomovar type

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prediction of Mortality in Patients with Cystic Fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Living donor lung transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Nutrition in patients with cystic fibrosis: a European Consensus

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Transplantation for cystic fibrosis: outcome following early liver transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

International comparison of median age at death from cystic fibrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2803%2912567-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0140-6736(03)12567-6

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12606185%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12606185%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

ResearchGate publication ID

0 references

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