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Inhaled versus nebulised tobramycin: A real world comparison in adult cystic fibrosis (CF)

Journal of cystic fibrosis, 2014-12, Vol.13 (6), p.692-698

2014

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Clostridium difficile carriage in adult cystic fibrosis (CF); implications for patients with CF and the potential for transmission of nosocomial infection

Journal of cystic fibrosis, 2017-03, Vol.16 (2), p.291-298

2017

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A bolt from the blue; A case report of an unusual asthma exacerbation

Respiratory medicine case reports, 2020-01, Vol.29, p.100983, Article 100983

2020

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Ivacaftor therapy in siblings with cystic fibrosis-the potential implications of Itraconazole in dosage and efficacy

Pulmonary pharmacology & therapeutics, 2015-04, Vol.31, p.49-50

2015

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157 Ivacaftor does not produce a significant change in anti-Pseudomonas aeruginosa antibodies

Journal of cystic fibrosis, 2017-06, Vol.16, p.S106-S106

2017

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WS07.6 Investigating the gut microbiota of patients with cystic fibrosis (PWCF) and the effects of an altered gut microbiota on functionality and faecal metabolites – the CFMATTERS experience

Journal of cystic fibrosis, 2016-06, Vol.15, p.S12-S12

2016

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200 Prevalence of dyslipidaemia in an Irish adult cystic fibrosis cohort

Journal of cystic fibrosis, 2014-06, Vol.13, p.S98-S98

2014

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289 Ageing in cystic fibrosis: a comparison of adult patients attending a tertiary referral centre

Journal of cystic fibrosis, 2014-06, Vol.13, p.S122-S122

2014

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201 Vitamin A deficiency: prevalence and clinical implications for adult cystic fibrosis

Journal of cystic fibrosis, 2014-06, Vol.13, p.S98-S98

2014

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217 Medical outcomes post transition of clinical care from a paediatric cystic fibrosis care model to an adult cystic fibrosis care model – an Irish perspective

Journal of cystic fibrosis, 2016-06, Vol.15, p.S106-S106

2016

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128 The metabolic consequences of CFTR modulation with ivacaftor in a single adult cystic fibrosis centre cohort

Journal of cystic fibrosis, 2015-06, Vol.14, p.S90-S90

2015

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48 Altered gut microbiota in stable patients with cystic fibrosis (CF) compared to controls and its relationship with intravenous (IV) antibiotic usage and lung function

Journal of cystic fibrosis, 2015-06, Vol.14, p.S69-S69

2015

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WS16.1 Clinical Outcomes of Real-World Kalydeco (CORK) study – Investigating the impact of CFTR potentiation on the intestinal microbiota, exocrine pancreatic function and intestinal inflammation prospectively over 12 months

Journal of cystic fibrosis, 2015-06, Vol.14, p.S29-S29

2015

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WS20.4 Clinical outcomes of Real-World Kalydeco (CORK) study – a prospective 12 month analysis addressing the impact of CFTR modulation on the cystic fibrosis lung

Journal of cystic fibrosis, 2015-06, Vol.14, p.S37-S37

2015

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Induction of Thymic Stromal Lymphopoietin (TSLP) in Airway Epithelium by Recombinant Allergens

Journal of allergy and clinical immunology, 2011-02, Vol.127 (2), p.AB125-AB125

2011

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131 The clinical implications of MRSA colonisation in a cohort of Irish adult cystic fibrosis (CF) patients and MRSA carrier frequency and clinical sequelae in their household contacts

Journal of cystic fibrosis, 2012-06, Vol.11, p.S89-S89

2012

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37 Clinical outcomes of real world Kalydeco (CORK) study

Journal of cystic fibrosis, 2014-06, Vol.13, p.S56-S56

2014

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254 The prognostic significance of hypoglycaemia on oral glucose tolerance tests in adults with cystic fibrosis (CF): A prospective clinical study

Journal of cystic fibrosis, 2013-06, Vol.12, p.S113-S113

2013

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74 Improved tolerability, adherence and reduced intravenous (IV) antibiotic usage in CF patients receiving inhaled versus nebulised antibiotic prophylaxis. A real world comparison of tobramycin inhaled powder (TIP) and tobramycin inhaled solution (TIS)

Journal of cystic fibrosis, 2013-06, Vol.12, p.S67-S67

2013

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WS8.1 The role of second-generation sequencing in describing the fungal microbiota in the adult cystic fibrosis (CF) airway and its correlation with clinical phenotype

Journal of cystic fibrosis, 2013-06, Vol.12, p.S16-S16

2013

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296 Why do adult patients with cystic fibrosis attend their general practitioner? A specialist CF centre's perspective

Journal of cystic fibrosis, 2012-06, Vol.11, p.S132-S132

2012

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P-103 Occult NRAS mutations with very low allele burden have independent prognostic significance in lower-risk myelodysplastic syndromes

Leukemia research, 2013-05, Vol.37, p.S68-S69

2013

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WS3.5 Clostridium difficile in adult cystic fibrosis (CF): Prevalence, ribotyping and toxigenic capability. A prospective study

Journal of cystic fibrosis, 2013-06, Vol.12, p.S6-S6

2013

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202 Nebuliser strategies in cystic fibrosis in Ireland. Results of a national audit

Journal of cystic fibrosis, 2012-06, Vol.11, p.S108-S108

2012

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Ligand tuning in the chromium–salen-mediated asymmetric epoxidation of alkenes

Tetrahedron: asymmetry, 2004-04, Vol.15 (8), p.1343-1354

2004

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Inhaled versus nebulised tobramycin: A real world comparison in adult cystic fibrosis (CF)

Clostridium difficile carriage in adult cystic fibrosis (CF); implications for patients with CF and the potential for transmission of nosocomial infection

A bolt from the blue; A case report of an unusual asthma exacerbation

Ivacaftor therapy in siblings with cystic fibrosis-the potential implications of Itraconazole in dosage and efficacy

157 Ivacaftor does not produce a significant change in anti-Pseudomonas aeruginosa antibodies

WS07.6 Investigating the gut microbiota of patients with cystic fibrosis (PWCF) and the effects of an altered gut microbiota on functionality and faecal metabolites – the CFMATTERS experience

200 Prevalence of dyslipidaemia in an Irish adult cystic fibrosis cohort

289 Ageing in cystic fibrosis: a comparison of adult patients attending a tertiary referral centre

201 Vitamin A deficiency: prevalence and clinical implications for adult cystic fibrosis

217 Medical outcomes post transition of clinical care from a paediatric cystic fibrosis care model to an adult cystic fibrosis care model – an Irish perspective

128 The metabolic consequences of CFTR modulation with ivacaftor in a single adult cystic fibrosis centre cohort

48 Altered gut microbiota in stable patients with cystic fibrosis (CF) compared to controls and its relationship with intravenous (IV) antibiotic usage and lung function

WS16.1 Clinical Outcomes of Real-World Kalydeco (CORK) study – Investigating the impact of CFTR potentiation on the intestinal microbiota, exocrine pancreatic function and intestinal inflammation prospectively over 12 months

WS20.4 Clinical outcomes of Real-World Kalydeco (CORK) study – a prospective 12 month analysis addressing the impact of CFTR modulation on the cystic fibrosis lung

Induction of Thymic Stromal Lymphopoietin (TSLP) in Airway Epithelium by Recombinant Allergens

131 The clinical implications of MRSA colonisation in a cohort of Irish adult cystic fibrosis (CF) patients and MRSA carrier frequency and clinical sequelae in their household contacts

37 Clinical outcomes of real world Kalydeco (CORK) study

254 The prognostic significance of hypoglycaemia on oral glucose tolerance tests in adults with cystic fibrosis (CF): A prospective clinical study

74 Improved tolerability, adherence and reduced intravenous (IV) antibiotic usage in CF patients receiving inhaled versus nebulised antibiotic prophylaxis. A real world comparison of tobramycin inhaled powder (TIP) and tobramycin inhaled solution (TIS)

WS8.1 The role of second-generation sequencing in describing the fungal microbiota in the adult cystic fibrosis (CF) airway and its correlation with clinical phenotype

296 Why do adult patients with cystic fibrosis attend their general practitioner? A specialist CF centre's perspective

P-103 Occult NRAS mutations with very low allele burden have independent prognostic significance in lower-risk myelodysplastic syndromes

WS3.5 Clostridium difficile in adult cystic fibrosis (CF): Prevalence, ribotyping and toxigenic capability. A prospective study

202 Nebuliser strategies in cystic fibrosis in Ireland. Results of a national audit

Ligand tuning in the chromium–salen-mediated asymmetric epoxidation of alkenes

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