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A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis

Journal of cystic fibrosis, 2009-01, Vol.8 (1), p.71-78

2009

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327 What parents want from parents' evenings

Journal of cystic fibrosis, 2013-06, Vol.12, p.S132-S132

2013

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WS6.6 A prospective multi centre study to examine the impact of home intravenous antibiotic treatment (H-IVAT) on carer well being

Journal of cystic fibrosis, 2013-06, Vol.12, p.S12-S12

2013

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346 A qualitative study to explore factors that impact adherence to aerosol therapy in young people with CF: Patient and parent perspectives

Journal of cystic fibrosis, 2013-06, Vol.12, p.S137-S137

2013

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Birth weight, feeding practices and pancreatic enzyme replacement therapy (PERT) in infants diagnosed with cystic fibrosis by newborn screening – 10 years experience

Journal of cystic fibrosis, 2010, Vol.9, p.S85-S85

2010

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Serum tobramycin levels following delivery of tobramycin (Tobi®) via eFlow® advanced nebuliser in children with cystic fibrosis

Journal of cystic fibrosis, 2010-07, Vol.9 (4), p.292-295

2010

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Can Burkholderia cepacia complex be eradicated with nebulised Amiloride and TOBI® ?

Journal of cystic fibrosis, 2010-01, Vol.9 (1), p.73-74

2010

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Processing a positive newborn screening result for cystic fibrosis (CF); a survey of UK practice

Journal of cystic fibrosis, 2010, Vol.9, p.S6-S6

2010

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Predictors of progression to chronic Pseudomonas aeruginosa (Pa) infection in children with CF classified in the intermittent Pa group

Journal of cystic fibrosis, 2010, Vol.9, p.S30-S30

2010

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Cystic fibrosis co-existing with trisomy 21

Journal of cystic fibrosis, 2010-09, Vol.9 (5), p.330-331

2010

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Adherence to nebulised therapies does not improve during school holidays for children with CF

Journal of cystic fibrosis, 2010, Vol.9, p.S102-S102

2010

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Sequential bronchoscopy in the management of patients with lobar atelectasis

Journal of cystic fibrosis, 2009, Vol.8, p.S69-S69

2009

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Can Burkholderia Cepacia complex (BCC) be eradicated with nebulised Amiloride and Tobi?

Journal of cystic fibrosis, 2009, Vol.8, p.S65-S65

2009

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Totally implanted venous access devices (TIVADs) in children with cystic fibrosis: Pilot satisfaction survey

Journal of cystic fibrosis, 2009, Vol.8, p.S93-S93

2009

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Serum tobramycin levels following delivery of tobramycin (TOBI®) via eFlow advanced nebuliser in children with cystic fibrosis

Journal of cystic fibrosis, 2009, Vol.8, p.S47-S47

2009

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101 Survival of Cepacia Syndrome

Journal of cystic fibrosis, 2007, Vol.6, p.S25-S25

2007

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373 Respiratory exacerbations in childhood associated with compound heterozygote CFTR genotype ΔF508/R117H on a background of 7T polythymidine tract at intron 8

Journal of cystic fibrosis, 2007, Vol.6, p.S91-S91

2007

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Implementation, uptake and impact of a cystic fibrosis electronic patient record system

Journal of cystic fibrosis, 2009, Vol.8, p.S109-S109

2009

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Geosmithia argillacea – a potential new pathogen in cystic fibrosis lung disease?

Journal of cystic fibrosis, 2008-06, Vol.7, p.S50-S50

2008

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Estimating risk associated with home-based intravenous antibiotic therapy (IVAT)

Journal of cystic fibrosis, 2009, Vol.8, p.S95-S95

2009

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WS08.6 Impact of triple therapy on IVantibiotic requirements in cystic fibrosis: combining evidence from a patient Registry and randomised trials

Journal of cystic fibrosis, 2021, Vol.20, p.S16-S17

2021

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WS18.2 The transition towards lung transplant for cystic fibrosis in the United Kingdom

Journal of cystic fibrosis, 2018-06, Vol.17, p.S33-S33

2018

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Isolation of the Fungus Geosmithia argillacea in Sputum of People with Cystic Fibrosis

Journal of Clinical Microbiology, 2010-07, Vol.48 (7), p.2615-2617

2010

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Clinical value of obtaining sputum and cough swab samples following inhaled hypertonic saline in children with cystic fibrosis

Pediatric pulmonology, 2004-07, Vol.38 (1), p.82-87

2004

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Drug resistance has not emerged despite increased use of antibiotic therapy for new acquisitions of pseudomonas aeruginosa in children with cystic fibrosis

Archives of disease in childhood, 2004-04, Vol.89 (4), p.A39

2004

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A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis

327 What parents want from parents' evenings

WS6.6 A prospective multi centre study to examine the impact of home intravenous antibiotic treatment (H-IVAT) on carer well being

346 A qualitative study to explore factors that impact adherence to aerosol therapy in young people with CF: Patient and parent perspectives

Birth weight, feeding practices and pancreatic enzyme replacement therapy (PERT) in infants diagnosed with cystic fibrosis by newborn screening – 10 years experience

Serum tobramycin levels following delivery of tobramycin (Tobi®) via eFlow® advanced nebuliser in children with cystic fibrosis

Can Burkholderia cepacia complex be eradicated with nebulised Amiloride and TOBI® ?

Processing a positive newborn screening result for cystic fibrosis (CF); a survey of UK practice

Predictors of progression to chronic Pseudomonas aeruginosa (Pa) infection in children with CF classified in the intermittent Pa group

Cystic fibrosis co-existing with trisomy 21

Adherence to nebulised therapies does not improve during school holidays for children with CF

Sequential bronchoscopy in the management of patients with lobar atelectasis

Can Burkholderia Cepacia complex (BCC) be eradicated with nebulised Amiloride and Tobi?

Totally implanted venous access devices (TIVADs) in children with cystic fibrosis: Pilot satisfaction survey

Serum tobramycin levels following delivery of tobramycin (TOBI®) via eFlow advanced nebuliser in children with cystic fibrosis

101 Survival of Cepacia Syndrome

373 Respiratory exacerbations in childhood associated with compound heterozygote CFTR genotype ΔF508/R117H on a background of 7T polythymidine tract at intron 8

Implementation, uptake and impact of a cystic fibrosis electronic patient record system

Geosmithia argillacea – a potential new pathogen in cystic fibrosis lung disease?

Estimating risk associated with home-based intravenous antibiotic therapy (IVAT)

WS08.6 Impact of triple therapy on IVantibiotic requirements in cystic fibrosis: combining evidence from a patient Registry and randomised trials

WS18.2 The transition towards lung transplant for cystic fibrosis in the United Kingdom

Isolation of the Fungus Geosmithia argillacea in Sputum of People with Cystic Fibrosis

Clinical value of obtaining sputum and cough swab samples following inhaled hypertonic saline in children with cystic fibrosis

Drug resistance has not emerged despite increased use of antibiotic therapy for new acquisitions of pseudomonas aeruginosa in children with cystic fibrosis

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