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Lung clearance index to detect the efficacy of Aztreonam lysine inhalation in patients with cystic fibrosis and near normal spirometry - A single-centre feasibility study

PloS one, 2019-09, Vol.14 (9), p.e0221673

2019

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Early and sustained improvements of lung clearance index from two to sixteen weeks of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis-a real world study

Frontiers in pharmacology, 2023-03, Vol.14, p.1125853

2023

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Malignancies in patients with cystic fibrosis: a case series

Journal of medical case reports, 2022-01, Vol.16 (1), p.27-27, Article 27

2022

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Add-on salmeterol compared to double dose fluticasone in pediatric asthma: A double-blind, randomized trial (VIAPAED)

Pediatric pulmonology, 2009-11, Vol.44 (11), p.1132-1142

2009

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Cancer in Cystic Fibrosis

Chest, 2022-05, Vol.161 (5), p.e325-e326

2022

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Reference Values Matter: Fewer Patients With Malnutrition Using American Compared to More Recent German Growth Charts

Journal of pediatric gastroenterology and nutrition, 2021-06, Vol.72 (6), p.912-915

2021

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Reference Values Matter

Journal of pediatric gastroenterology and nutrition, 2021-06, Vol.72 (6), p.912-915

2021

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Arm muscle area for the longitudinal assessment of nutritional status in paediatric patients with cystic fibrosis - A single centre experience

Journal of cystic fibrosis, 2022-03, Vol.21 (2), p.e122-e128

2022

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Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters: A Longitudinal Analysis for 12 Years

Journal of pediatric gastroenterology and nutrition, 2017-10, Vol.65 (4), p.438-442

2017

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Cancer in Cystic Fibrosis: Do Not Neglect Gynecologic Cancers

Chest, 2022-05, Vol.161 (5), p.e325-e326

2022

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Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project

Thorax, 2002-07, Vol.57 (7), p.596-601

2002

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Faecal calprotectin concentrations in young children with cystic fibrosis

Journal of cystic fibrosis, 2018-01, Vol.17 (1), p.e8-e9

2018

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Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters

Journal of pediatric gastroenterology and nutrition, 2017-10, Vol.65 (4), p.438-442

2017

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Tracking Lung Clearance Index and chest CT in mild cystic fibrosis lung disease over a period of three years

Respiratory medicine, 2014-06, Vol.108 (6), p.865-874

2014

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Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?

Journal of cystic fibrosis, 2016-01, Vol.15 (1), p.123-126

2016

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The ideal and the real world of mental health care delivery

Journal of cystic fibrosis, 2015-11, Vol.14 (6), p.e33-e34

2015

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Sensitivity of lung clearance index and chest computed tomography in early cf lung disease

Respiratory medicine, 2010-12, Vol.104 (12), p.1834-1842

2010

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Evaluating patient experience in a cystic fibrosis centre using a disease-specific patient satisfaction questionnaire

European journal of pediatrics, 2015-11, Vol.174 (11), p.1451-1460

2015

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COPD, die Systemerkrankung: Ernährung: zu wenig beachtet und noch ungelöst

Pneumologie (Stuttgart, Germany), 2003-11, Vol.57 (11), p.681-689

Steinkamp, Gratiana

2003

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COPD, die Systemerkrankung: Ernährung: zu wenig beachtet und noch ungelöst

Pneumologie (Stuttgart, Germany), 2003-12, Vol.57 (12), p.733-733

Steinkamp, Gratiana

2003

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COPD, the systemic disease: nutrition - an underestimated and unresolved problem

Pneumologie (Stuttgart, Germany), 2003-11, Vol.57 (11), p.681-689

Steinkamp, Gratiana

2003

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Different approaches to evaluate patient experience and satisfaction in CF centres

Journal of cystic fibrosis, 2015-09, Vol.14 (5), p.E19-E20

2015

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COPD und Schlaf

Pneumologie (Stuttgart, Germany), 2006-10, Vol.60 (10), p.642-651

2006

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Cystic fibrosis (CF) care through the patients' eyes – A nationwide survey on experience and satisfaction with services using a disease-specific questionnaire

Respiratory medicine, 2015-01, Vol.109 (1), p.79-87

2015

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Neue Entwicklungen im Gesundheitssystem und ihre Auswirkungen auf die Pneumologie

Pneumologie (Stuttgart, Germany), 2005-03, Vol.59 (3), p.204-212

Steinkamp, G.

2005

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Lung clearance index to detect the efficacy of Aztreonam lysine inhalation in patients with cystic fibrosis and near normal spirometry - A single-centre feasibility study

Early and sustained improvements of lung clearance index from two to sixteen weeks of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis-a real world study

Malignancies in patients with cystic fibrosis: a case series

Add-on salmeterol compared to double dose fluticasone in pediatric asthma: A double-blind, randomized trial (VIAPAED)

Cancer in Cystic Fibrosis

Reference Values Matter: Fewer Patients With Malnutrition Using American Compared to More Recent German Growth Charts

Reference Values Matter

Arm muscle area for the longitudinal assessment of nutritional status in paediatric patients with cystic fibrosis - A single centre experience

Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters: A Longitudinal Analysis for 12 Years

Cancer in Cystic Fibrosis: Do Not Neglect Gynecologic Cancers

Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project

Faecal calprotectin concentrations in young children with cystic fibrosis

Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters

Tracking Lung Clearance Index and chest CT in mild cystic fibrosis lung disease over a period of three years

Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?

The ideal and the real world of mental health care delivery

Sensitivity of lung clearance index and chest computed tomography in early cf lung disease

Evaluating patient experience in a cystic fibrosis centre using a disease-specific patient satisfaction questionnaire

COPD, die Systemerkrankung: Ernährung: zu wenig beachtet und noch ungelöst

COPD, die Systemerkrankung: Ernährung: zu wenig beachtet und noch ungelöst

COPD, the systemic disease: nutrition - an underestimated and unresolved problem

Different approaches to evaluate patient experience and satisfaction in CF centres

COPD und Schlaf

Cystic fibrosis (CF) care through the patients' eyes – A nationwide survey on experience and satisfaction with services using a disease-specific questionnaire

Neue Entwicklungen im Gesundheitssystem und ihre Auswirkungen auf die Pneumologie

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