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Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis

Journal of applied physiology (1985), 2007-05, Vol.102 (5), p.1969-1975

2007

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HbA1c as a screening tool for cystic fibrosis related diabetes

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.251-257

2016

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Short-term comparative study of high frequency chest wall oscillation and European airway clearance techniques in patients with cystic fibrosis

Thorax, 2010-03, Vol.65 (3), p.196-200

2010

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Growing old with cystic fibrosis – The characteristics of long-term survivors of cystic fibrosis

Respiratory medicine, 2009-04, Vol.103 (4), p.629-635

2009

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Nasal and Exhaled Nitric Oxide Is Reduced in Adult Patients With Cystic Fibrosis and Does Not Correlate With Cystic Fibrosis Genotype

Chest, 2000-04, Vol.117 (4), p.1085-1089

2000

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Airway glucose concentrations and effect on growth of respiratory pathogens in cystic fibrosis

Journal of cystic fibrosis, 2007-04, Vol.6 (2), p.101-109

2007

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Right Ventricular Dysfunction in Adult Severe Cystic Fibrosis

Chest, 2000-10, Vol.118 (4), p.1063-1068

2000

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Increased Leukotriene B4 and Interleukin-6 in Exhaled Breath Condensate in Cystic Fibrosis

American journal of respiratory and critical care medicine, 2003-04, Vol.167 (8), p.1109-1112

2003

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The prevalence of “risky behaviour” in adults with cystic fibrosis

Journal of cystic fibrosis, 2012-01, Vol.11 (1), p.56-58

2012

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Exhaled 8-isoprostane as a new non-invasive biomarker of oxidative stress in cystic fibrosis

Thorax, 2000-03, Vol.55 (3), p.205-209

2000

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Response to Letter to the Editor: HbA1c as a screening tool for cystic fibrosis related diabetes: Response to letters by Widger et al. and Schnyder et al

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.265-266

2016

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Predicting survival in end-stage cystic fibrosis

Respiratory medicine, 2009-10, Vol.103 (10), p.1441-1447

2009

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Response to Letter to the Editor: HbA1c as a screening tool for cystic fibrosis related diabetes

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.265-266

2016

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A woman with cystic fibrosis, severe hypoxaemia, an atrial thrombus and a patent foramen ovale: a case report

Journal of medical case reports, 2009-07, Vol.3 (1), p.8582-8582

2009

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Musculoskeletal techniques for clinically stable adults with cystic fibrosis: a preliminary randomised controlled trial

Physiotherapy, 2011-09, Vol.97 (3), p.209-217

2011

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A feasibility study of home telemedicine for patients with cystic fibrosis awaiting transplantation

Journal of telemedicine and telecare, 2008-06, Vol.14 (4), p.182-185

2008

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An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years

Journal of cystic fibrosis, 2008-11, Vol.7 (6), p.537-542

2008

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Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Nature medicine, 1995-01, Vol.1 (1), p.39-46

1995

Volltextzugriff (PDF)

Histomorphometric Analysis of Bone Biopsies from the Iliac Crest of Adults with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2002-12, Vol.166 (11), p.1470-1474

2002

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Pregnancy in cystic fibrosis lung transplant recipients: Case series and review

Journal of cystic fibrosis, 2006-08, Vol.5 (3), p.171-175

2006

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Adult cystic fibrosis patients with and without infective exacerbations and their factor XII levels

Blood coagulation & fibrinolysis, 2009-09, Vol.20 (6), p.400-402

2009

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Role of CT in the Management of Pneumothorax in Patients with Complex Cystic Lung Disease

Chest, 1997-07, Vol.112 (1), p.275-278

1997

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Increase in exhaled carbon monoxide during exacerbations of cystic fibrosis

Thorax, 2000-02, Vol.55 (2), p.138-142

2000

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Exhaled ethane is elevated in cystic fibrosis and correlates with carbon monoxide levels and airway obstruction

American journal of respiratory and critical care medicine, 2000-04, Vol.161 (4), p.1247-1251

2000

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Open follow-up study of tobramycin nebuliser solution and colistin in patients with cystic fibrosis

Journal of cystic fibrosis, 2006-12, Vol.5 (4), p.261-263

2006

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Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis

HbA1c as a screening tool for cystic fibrosis related diabetes

Short-term comparative study of high frequency chest wall oscillation and European airway clearance techniques in patients with cystic fibrosis

Growing old with cystic fibrosis – The characteristics of long-term survivors of cystic fibrosis

Nasal and Exhaled Nitric Oxide Is Reduced in Adult Patients With Cystic Fibrosis and Does Not Correlate With Cystic Fibrosis Genotype

Airway glucose concentrations and effect on growth of respiratory pathogens in cystic fibrosis

Right Ventricular Dysfunction in Adult Severe Cystic Fibrosis

Increased Leukotriene B4 and Interleukin-6 in Exhaled Breath Condensate in Cystic Fibrosis

The prevalence of “risky behaviour” in adults with cystic fibrosis

Exhaled 8-isoprostane as a new non-invasive biomarker of oxidative stress in cystic fibrosis

Response to Letter to the Editor: HbA1c as a screening tool for cystic fibrosis related diabetes: Response to letters by Widger et al. and Schnyder et al

Predicting survival in end-stage cystic fibrosis

Response to Letter to the Editor: HbA1c as a screening tool for cystic fibrosis related diabetes

A woman with cystic fibrosis, severe hypoxaemia, an atrial thrombus and a patent foramen ovale: a case report

Musculoskeletal techniques for clinically stable adults with cystic fibrosis: a preliminary randomised controlled trial

A feasibility study of home telemedicine for patients with cystic fibrosis awaiting transplantation

An international/multicentre report on patients with cystic fibrosis (CF) over the age of 40 years

Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Histomorphometric Analysis of Bone Biopsies from the Iliac Crest of Adults with Cystic Fibrosis

Pregnancy in cystic fibrosis lung transplant recipients: Case series and review

Adult cystic fibrosis patients with and without infective exacerbations and their factor XII levels

Role of CT in the Management of Pneumothorax in Patients with Complex Cystic Lung Disease

Increase in exhaled carbon monoxide during exacerbations of cystic fibrosis

Exhaled ethane is elevated in cystic fibrosis and correlates with carbon monoxide levels and airway obstruction

Open follow-up study of tobramycin nebuliser solution and colistin in patients with cystic fibrosis

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