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The pharmacokinetics and toxicity of morning vs. evening tobramycin dosing for pulmonary exacerbations of cystic fibrosis: A randomised comparison

Journal of cystic fibrosis, 2016-07, Vol.15 (4), p.510-517

2016

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115 Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis – Cochrane review

Journal of cystic fibrosis, 2015-06, Vol.14, p.S86-S86

2015

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Compliance with mandatory reporting of clinical trial results on ClinicalTrials.gov: cross sectional study

BMJ (Online), 2012-01, Vol.344 (7838), p.d7373

International edition, 2012

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313 An international study of survival of children with cystic fibrosis after the first episode of invasive mechanical ventilation

Journal of cystic fibrosis, 2015-06, Vol.14, p.S138-S138

2015

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Delayed publication of clinical trials in cystic fibrosis

Journal of cystic fibrosis, 2012-01, Vol.11 (1), p.14-17

2012

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P235 A UK registry study of prophylactic antibiotic use for Staphylococcus aureus in children with cystic fibrosis

Thorax, 2011-12, Vol.66 (Suppl 4), p.A163-A163

2011

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304 Premature vascular ageing in children with cystic fibrosis (CF)

Journal of cystic fibrosis, 2013-06, Vol.12, p.S126-S126

2013

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Side effects of aminoglycosides on the kidney, ear and balance in cystic fibrosis

Thorax, 2010-07, Vol.65 (7), p.654-658

2010

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WS23.6 Assessment of renal function in cystic fibrosis patients by estimated and measured glomerular filtration rate – a cross-sectional study

Journal of cystic fibrosis, 2012-06, Vol.11, p.S52-S52

2012

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P09 The Use of Cochrane Reviews in Clinical Guidelines For Respiratory Disease in Children in the United Kingdom – a Systematic Review

Archives of disease in childhood, 2013-06, Vol.98 (Suppl 1), p.A5-A5

2013

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Trends in the incidence of acute kidney injury in UK cystic fibrosis patients

Journal of cystic fibrosis, 2010, Vol.9, p.S111-S111

2010

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P272 The effect of CFTR modulators on bilirubin levels in paediatrics: comparison of bilirubin levels before, and after commencement of elexacaftor/tezacaftor/ivacaftor (ETI)

Journal of cystic fibrosis, 2024-06, Vol.23, p.S152-S152

2024

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EPS7.03 Evaluating a novel MRI measure of lung ventilation in 6 to 11 year olds before and after elexacaftor/tezacaftor/ivacaftor: Preliminary results from the CIFT-CF Junior study

Journal of cystic fibrosis, 2024-06, Vol.23, p.S54-S54

2024

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WS08.03 Evaluating lung, liver and gut structure and function using MRI in 6 to 11 year olds – preliminary results from the GIFT-cystic fibrosis junior cohort

Journal of cystic fibrosis, 2023-06, Vol.22, p.S17-S17

2023

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G529(P) Flow rate as a predictor of weaning home oxygen in babies with bronchopulmonary dysplasia

Archives of disease in childhood, 2016-04, Vol.101 (Suppl 1), p.A312-A312

2016

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A healthy nation: strengthening child health research in the UK

The Lancet (British edition), 2013-01, Vol.381 (9860), p.73-87

2013

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Is cystic fibrosis survival improving in excess to that of the general population for England and Wales and the USA?

Archives of disease in childhood, 2012-05, Vol.97 (Suppl 1), p.A26-A26

2012

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Looking under the bonnet of bronchopulmonary dysplasia with MRI

Thorax, 2020-02, Vol.75 (2), p.100

2020

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Prebiotics for people with cystic fibrosis

Cochrane database of systematic reviews, 2023-09, Vol.9, p.CD015236

2023

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Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis

Cochrane database of systematic reviews, 2015-07, Vol.2015 (7), p.CD009730

2015

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Respiratory problems in children with Down syndrome

Paediatrics and child health, 2021-07, Vol.31 (7), p.271-275

2021

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P261 Infection, prevention and control in cystic fibrosis: an update of a systematic review of interventions

Journal of cystic fibrosis, 2024-06, Vol.23, p.S148-S148

2024

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Assessing the impact of posture on diaphragm morphology and function using an open upright MRI system—A pilot study

European journal of radiology, 2020-09, Vol.130, p.109196-109196, Article 109196

2020

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Bronchopulmonary dysplasia prediction models: a systematic review and meta-analysis with validation

Pediatric research, 2023-07, Vol.94 (1), p.43-54

2023

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Postprandial changes in gastrointestinal function and transit in cystic fibrosis assessed by Magnetic Resonance Imaging

Journal of cystic fibrosis, 2021-07, Vol.20 (4), p.591-597

2021

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The pharmacokinetics and toxicity of morning vs. evening tobramycin dosing for pulmonary exacerbations of cystic fibrosis: A randomised comparison

115 Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis – Cochrane review

Compliance with mandatory reporting of clinical trial results on ClinicalTrials.gov: cross sectional study

313 An international study of survival of children with cystic fibrosis after the first episode of invasive mechanical ventilation

Delayed publication of clinical trials in cystic fibrosis

P235 A UK registry study of prophylactic antibiotic use for Staphylococcus aureus in children with cystic fibrosis

304 Premature vascular ageing in children with cystic fibrosis (CF)

Side effects of aminoglycosides on the kidney, ear and balance in cystic fibrosis

WS23.6 Assessment of renal function in cystic fibrosis patients by estimated and measured glomerular filtration rate – a cross-sectional study

P09 The Use of Cochrane Reviews in Clinical Guidelines For Respiratory Disease in Children in the United Kingdom – a Systematic Review

Trends in the incidence of acute kidney injury in UK cystic fibrosis patients

P272 The effect of CFTR modulators on bilirubin levels in paediatrics: comparison of bilirubin levels before, and after commencement of elexacaftor/tezacaftor/ivacaftor (ETI)

EPS7.03 Evaluating a novel MRI measure of lung ventilation in 6 to 11 year olds before and after elexacaftor/tezacaftor/ivacaftor: Preliminary results from the CIFT-CF Junior study

WS08.03 Evaluating lung, liver and gut structure and function using MRI in 6 to 11 year olds – preliminary results from the GIFT-cystic fibrosis junior cohort

G529(P) Flow rate as a predictor of weaning home oxygen in babies with bronchopulmonary dysplasia

A healthy nation: strengthening child health research in the UK

Is cystic fibrosis survival improving in excess to that of the general population for England and Wales and the USA?

Looking under the bonnet of bronchopulmonary dysplasia with MRI

Prebiotics for people with cystic fibrosis

Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis

Respiratory problems in children with Down syndrome

P261 Infection, prevention and control in cystic fibrosis: an update of a systematic review of interventions

Assessing the impact of posture on diaphragm morphology and function using an open upright MRI system—A pilot study

Bronchopulmonary dysplasia prediction models: a systematic review and meta-analysis with validation

Postprandial changes in gastrointestinal function and transit in cystic fibrosis assessed by Magnetic Resonance Imaging

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