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Long-term effects of a partially supervised conditioning programme in cystic fibrosis

The European respiratory journal, 2010-03, Vol.35 (3), p.578-583

2010

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IPD2.12 Respiratory physiotherapy for children with cystic fibrosis at infancy and early childhood – an actual state-target-analysis in consideration of parental influences on therapy adherence

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

2017

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Physical activity is independently related to aerobic capacity in cystic fibrosis

The European respiratory journal, 2006-10, Vol.28 (4), p.734-739

2006

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A novel sidestream ultrasonic flow sensor for multiple breath washout in children

Pediatric pulmonology, 2008-08, Vol.43 (8), p.731-738

2008

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WS09.3 Professional quality of life among CF healthcare providers

Journal of cystic fibrosis, 2015-06, Vol.14, p.S17-S17

2015

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ePS05.7 Individual caloric intake in cystic fibrosis (CF) – how to calculate?

Journal of cystic fibrosis, 2015-06, Vol.14, p.S51-S51

2015

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Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patients

Infection, 2009-10, Vol.37 (5), p.424-431

2009

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253 Phase angle (PA) from bioelectrical impedance analysis (BIA) in children with cystic fibrosis (CF)

Journal of cystic fibrosis, 2012-06, Vol.11, p.S121-S121

2012

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280 VEMSE-CF: psychosocial characteristics of patients participating in a prospective controlled care research study

Journal of cystic fibrosis, 2014-06, Vol.13, p.S119-S119

2014

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Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome

Clinical and experimental immunology, 2009-02, Vol.155 (2), p.189-198

2009

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202 Exercise testing in children with cystic fibrosis (CF) – risk for adverse events?

Journal of cystic fibrosis, 2011, Vol.10, p.S51-S51

2011

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CF and sport – encouraging the motivation by a specific sport program

Journal of cystic fibrosis, 2010, Vol.9, p.S71-S71

2010

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P293 Physical activity in children and adolescents with cystic fibrosis – do they move enough?

Journal of cystic fibrosis, 2020-06, Vol.19, p.S138-S138

2020

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P321 Respiratory physiotherapy for children and adolescents with cystic fibrosis – is there a link between adherence and clinical health status?

Journal of cystic fibrosis, 2020-06, Vol.19, p.S145-S146

2020

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P469 From paediatric to adult care - improvement of a structural program of transition at the Cystic Fibrosis Centre of Hannover Medical School

Journal of cystic fibrosis, 2019-06, Vol.18, p.S190-S190

2019

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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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Recurrence of PSA after early treatment: a long-term follow-up study

Journal of cystic fibrosis, 2008-06, Vol.7, p.S33-S33

2008

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52 Protein analysis of mutant CFTR in human tissues

Journal of cystic fibrosis, 2011, Vol.10, p.S13-S13

2011

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Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11·2 microdeletion and partial DiGeorge syndrome

Clinical and experimental immunology, 2009-02, Vol.155 (2), p.189-198

2009

Volltextzugriff (PDF)

WS5.1 Inhaled glutathione in cystic fibrosis

Journal of cystic fibrosis, 2012-06, Vol.11, p.S11-S11

2012

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P201 Adherence in nebulisation therapy of paediatric patients with cystic fibrosis

Journal of cystic fibrosis, 2019-06, Vol.18, p.S114-S114

2019

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TIDES-CF Study: Who participates in psychosocial trials?

Journal of cystic fibrosis, 2009, Vol.8, p.S90-S90

2009

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P053 Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depend on age and lung disease severity

Journal of cystic fibrosis, 2023-06, Vol.22, p.S79-S79

2023

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Low-dose methotrexate for advanced pulmonary disease in patients with cystic fibrosis

Respiratory medicine, 2003-05, Vol.97 (5), p.498-500

2003

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Long-term effects of a partially supervised conditioning programme in cystic fibrosis

IPD2.12 Respiratory physiotherapy for children with cystic fibrosis at infancy and early childhood – an actual state-target-analysis in consideration of parental influences on therapy adherence

Physical activity is independently related to aerobic capacity in cystic fibrosis

A novel sidestream ultrasonic flow sensor for multiple breath washout in children

WS09.3 Professional quality of life among CF healthcare providers

ePS05.7 Individual caloric intake in cystic fibrosis (CF) – how to calculate?

Tobramycin once- vs thrice-daily for elective intravenous antipseudomonal therapy in pediatric cystic fibrosis patients

253 Phase angle (PA) from bioelectrical impedance analysis (BIA) in children with cystic fibrosis (CF)

280 VEMSE-CF: psychosocial characteristics of patients participating in a prospective controlled care research study

Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome

202 Exercise testing in children with cystic fibrosis (CF) – risk for adverse events?

CF and sport – encouraging the motivation by a specific sport program

P293 Physical activity in children and adolescents with cystic fibrosis – do they move enough?

P321 Respiratory physiotherapy for children and adolescents with cystic fibrosis – is there a link between adherence and clinical health status?

P469 From paediatric to adult care - improvement of a structural program of transition at the Cystic Fibrosis Centre of Hannover Medical School

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

Recurrence of PSA after early treatment: a long-term follow-up study

52 Protein analysis of mutant CFTR in human tissues

Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11·2 microdeletion and partial DiGeorge syndrome

WS5.1 Inhaled glutathione in cystic fibrosis

1535P Paclitaxel + ramucirumab versus paclitaxel alone in patients with squamous-cell carcinoma of the oesophagus, refractory or intolerant to combination therapy with fluoropyrimidine and platinum-based drugs: Final results from the randomized phase II IKF-S627/RAMOS trial of the AIO

P201 Adherence in nebulisation therapy of paediatric patients with cystic fibrosis

TIDES-CF Study: Who participates in psychosocial trials?

P053 Spirometric and anthropometric improvements in response to elexacaftor/tezacaftor/ivacaftor depend on age and lung disease severity

Low-dose methotrexate for advanced pulmonary disease in patients with cystic fibrosis

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