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Helmut Ellemunter

Showing results (11-20 of 59) with videos related to

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Clinical Case Reports|February 14, 2022
REAL-world clinical effectiveness of ivacaftor therapy in the first 24 months in two infants with cystic fibrosis and different gating mutations-A case reportTeresa Fuchs, Dorothea Appelt, Katharina Niedermayr, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 14, 2015
Different approaches to evaluate patient experience and satisfaction in CF centresGratiana Steinkamp, Helmut Ellemunter, Carsten Schwarz, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 17, 2017
Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters: A Longitudinal Analysis for 12 YearsHelmut Ellemunter, Alexander Engelhardt, Katharina Schüller, et al.
Pediatric Pulmonology|November 14, 2009
Lung clearance index: normal values, repeatability, and reproducibility in healthy children and adolescentsSusanne I Fuchs, Johannes Eder, Helmut Ellemunter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 21, 2015
Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?Helmut Ellemunter, Johannes Eder, Susanne Fuchs, et al.
Pediatric Pulmonology|December 17, 2008
Hygienic safety of an ultrasonic flow sensor for multiple breath washoutSusanne I Fuchs, Monika Gappa, Maria Waltner-Romen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 18, 2012
Calculation of the capnographic index based on expiratory molar mass-volume-curves--a suitable tool to screen for cystic fibrosis lung diseaseSusanne I Fuchs, Sibylle Junge, Helmut Ellemunter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 29, 2025
Monitoring ETI effects over 1.7 years in an infant treated in utero, via breast milk and granules by repeated faecal elastase measurementsDorothea Appelt, Teresa Fuchs, Johannes Eder, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 22, 2015
Psychological resilience and intolerance of uncertainty in coping with cystic fibrosisHorst Mitmansgruber, Ulrike Smrekar, Bianca Rabanser, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patientsCarla Colombo, Helmut Ellemunter, Roderick Houwen, et al.
Pageof 6

Showing results (11-20 of 59) with videos related to

Sort By:
Pageof 6
Clinical Case Reports|February 14, 2022
REAL-world clinical effectiveness of ivacaftor therapy in the first 24 months in two infants with cystic fibrosis and different gating mutations-A case reportTeresa Fuchs, Dorothea Appelt, Katharina Niedermayr, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 14, 2015
Different approaches to evaluate patient experience and satisfaction in CF centresGratiana Steinkamp, Helmut Ellemunter, Carsten Schwarz, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 17, 2017
Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters: A Longitudinal Analysis for 12 YearsHelmut Ellemunter, Alexander Engelhardt, Katharina Schüller, et al.
Pediatric Pulmonology|November 14, 2009
Lung clearance index: normal values, repeatability, and reproducibility in healthy children and adolescentsSusanne I Fuchs, Johannes Eder, Helmut Ellemunter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 21, 2015
Long-term improvement of lung clearance index in patients with mild cystic fibrosis lung disease: Does hypertonic saline play a role?Helmut Ellemunter, Johannes Eder, Susanne Fuchs, et al.
Pediatric Pulmonology|December 17, 2008
Hygienic safety of an ultrasonic flow sensor for multiple breath washoutSusanne I Fuchs, Monika Gappa, Maria Waltner-Romen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 18, 2012
Calculation of the capnographic index based on expiratory molar mass-volume-curves--a suitable tool to screen for cystic fibrosis lung diseaseSusanne I Fuchs, Sibylle Junge, Helmut Ellemunter, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 29, 2025
Monitoring ETI effects over 1.7 years in an infant treated in utero, via breast milk and granules by repeated faecal elastase measurementsDorothea Appelt, Teresa Fuchs, Johannes Eder, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 22, 2015
Psychological resilience and intolerance of uncertainty in coping with cystic fibrosisHorst Mitmansgruber, Ulrike Smrekar, Bianca Rabanser, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
Guidelines for the diagnosis and management of distal intestinal obstruction syndrome in cystic fibrosis patientsCarla Colombo, Helmut Ellemunter, Roderick Houwen, et al.
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