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Patterns and predictors of sleep disordered breathing in primary myopathies

Thorax, 2002-08, Vol.57 (8), p.724-728

2002

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177 Long-term efficacy and adherence of colistin dry powder inhalation (CDPI) at a large German CF adult unit – real world experience

Journal of cystic fibrosis, 2017-06, Vol.16, p.S112-S112

2017

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Predictors of severe chest infections in pediatric neuromuscular disorders

Neuromuscular disorders : NMD, 2006-05, Vol.16 (5), p.325-328

2006

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Long-term noninvasive ventilation in children and adolescents with neuromuscular disorders

The European respiratory journal, 2003-10, Vol.22 (4), p.631-636

2003

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Respiratory failure in Pompe disease: treatment with noninvasive ventilation

Neurology, 2005-04, Vol.64 (8), p.1465-1467

2005

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Sleep-disordered breathing and respiratory failure in acid maltase deficiency

Neurology, 2001-10, Vol.57 (7), p.1290-1295

2001

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123 Colobreathe® dry powder inhaler (CSDPI) – improved adherence due to personal guidance by a respiratory therapist

Journal of cystic fibrosis, 2016-06, Vol.15, p.S82-S82

2016

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Non-invasive ventilation reduces respiratory tract infections in children with neuromuscular disorders

Pediatric pulmonology, 2008-01, Vol.43 (1), p.67-71

2008

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S2k-Leitlinie: Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen Insuffizienz – Revision 2017

Pneumologie (Stuttgart, Germany), 2017-11, Vol.71 (11), p.722-795

2017

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WS04.4 Balance, flexibility and agility – additional aspects of physical fitness and trainability in children and adolescents with CF

Journal of cystic fibrosis, 2017-06, Vol.16, p.S7-S7

2017

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IPD2.13 Reasons for non-attendance in sport/activity program (CF mobil) in cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S61-S62

2017

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WS09.1 Balance, flexibility and agility – additional aspects of physical fitness in children with cystic fibrosis (CF)

Journal of cystic fibrosis, 2016-06, Vol.15, p.S14-S14

2016

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ePS04.6 Barrier and barrier management in sports in cystic fibrosis (CF)

Journal of cystic fibrosis, 2016-06, Vol.15, p.S44-S45

2016

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Stenotrophomonas maltophilia in cystic fibrosis: Improved detection by the use of selective agar and evaluation of antimicrobial resistance

Journal of cystic fibrosis, 2011-12, Vol.10 (6), p.422-427

2011

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Development of a quantitative immunofluorescence assay for detection of Stenotrophomonas maltophilia antibodies in patients with cystic fibrosis

Journal of cystic fibrosis, 2013-12, Vol.12 (6), p.651-654

2013

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Airway clearance techniques in neuromuscular disorders: A state of the art review

Respiratory medicine, 2018-03, Vol.136, p.98-110

2018

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G.P.72 Myasthenic symptoms: From initial presentation to diagnosis

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.856-856

2012

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Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen Insuffizienz

Pneumologie (Stuttgart, Germany), 2010-04, Vol.64 (4), p.207-240

2010

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Chronic respiratory failure and work of breathing in children with progressive neuromuscular disorders

Paediatric respiratory reviews, 2010, Vol.11, p.S102-S102

2010

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Interrelationships between lung clearance index and parameters of lung function and gas exchange in patients with cystic fibrosis

Paediatric respiratory reviews, 2010, Vol.11, p.S99-S99

2010

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91 Sequential inhalative tobramycin–colistin-combination stabilizes patients with chronic Pseudomonas aeruginosa colonization

Journal of cystic fibrosis, 2013-06, Vol.12, p.S71-S71

2013

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WS10.05 Physical fitness and habitual physical activity in adults with cystic fibrosis - do they improve with elexacaftor/tezacaftor/ivacaftor therapy?

Journal of cystic fibrosis, 2022-06, Vol.21, p.S20

2022

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39. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie e.V.; Essen, 30. März – 1. April 2017

Atemwegs- und Lungenkrankheiten, 2017-03, Vol.43 (3), p.99-136

2017

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Technical cough assist improves ventilation inhomogeneity in NMD

Paediatric respiratory reviews, 2011, Vol.12, p.S86-S86

2011

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WS19.9 A prospective multicenter study to dissect Staphylococcus aureus-colonization from infection in cystic fibrosis patients

Journal of cystic fibrosis, 2013-06, Vol.12, p.S40-S40

2013

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Patterns and predictors of sleep disordered breathing in primary myopathies

177 Long-term efficacy and adherence of colistin dry powder inhalation (CDPI) at a large German CF adult unit – real world experience

Predictors of severe chest infections in pediatric neuromuscular disorders

Long-term noninvasive ventilation in children and adolescents with neuromuscular disorders

Respiratory failure in Pompe disease: treatment with noninvasive ventilation

Sleep-disordered breathing and respiratory failure in acid maltase deficiency

123 Colobreathe® dry powder inhaler (CSDPI) – improved adherence due to personal guidance by a respiratory therapist

Non-invasive ventilation reduces respiratory tract infections in children with neuromuscular disorders

S2k-Leitlinie: Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen Insuffizienz – Revision 2017

WS04.4 Balance, flexibility and agility – additional aspects of physical fitness and trainability in children and adolescents with CF

IPD2.13 Reasons for non-attendance in sport/activity program (CF mobil) in cystic fibrosis

WS09.1 Balance, flexibility and agility – additional aspects of physical fitness in children with cystic fibrosis (CF)

ePS04.6 Barrier and barrier management in sports in cystic fibrosis (CF)

Stenotrophomonas maltophilia in cystic fibrosis: Improved detection by the use of selective agar and evaluation of antimicrobial resistance

Development of a quantitative immunofluorescence assay for detection of Stenotrophomonas maltophilia antibodies in patients with cystic fibrosis

Airway clearance techniques in neuromuscular disorders: A state of the art review

G.P.72 Myasthenic symptoms: From initial presentation to diagnosis

Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen Insuffizienz

Chronic respiratory failure and work of breathing in children with progressive neuromuscular disorders

Interrelationships between lung clearance index and parameters of lung function and gas exchange in patients with cystic fibrosis

91 Sequential inhalative tobramycin–colistin-combination stabilizes patients with chronic Pseudomonas aeruginosa colonization

WS10.05 Physical fitness and habitual physical activity in adults with cystic fibrosis - do they improve with elexacaftor/tezacaftor/ivacaftor therapy?

39. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie e.V.; Essen, 30. März – 1. April 2017

Technical cough assist improves ventilation inhomogeneity in NMD

WS19.9 A prospective multicenter study to dissect Staphylococcus aureus-colonization from infection in cystic fibrosis patients

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