Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Leonie A Tepper"'
Autor:
Elisabeth M. W. J. Utens, Alexandra L. Quittner, Pierluigi Ciet, Leonie A. Tepper, Daan Caudri, Harm A.W.M. Tiddens
Publikováno v:
Pediatric Pulmonology. 51:34-41
Summary Background Computed Tomography (CT) is the gold standard to assess bronchiectasis and trapped air in cystic fibrosis (CF) lung disease, but has the disadvantage of radiation exposure. Magnetic Resonance Imaging (MRI) is a radiation free alter
Autor:
Alexandra L. Quittner, Leonie A. Tepper, Elisabeth M. W. J. Utens, Els C. van der Wiel, Daan Caudri, Harm A.W.M. Tiddens
Publikováno v:
Pediatric Pulmonology. 49:1182-1189
Summary Introduction Cystic fibrosis (CF) lung disease is characterized by bronchiectasis and trapped air on chest computed tomography (CT). Objective We aim to validate bronchiectasis and trapped air as outcome measures by evaluating associations be
Autor:
Leonie A, Tepper, Pierluigi, Ciet, Daan, Caudri, Alexandra L, Quittner, Elisabeth M W J, Utens, Harm A W M, Tiddens
Publikováno v:
Pediatric pulmonology. 51(1)
Computed Tomography (CT) is the gold standard to assess bronchiectasis and trapped air in cystic fibrosis (CF) lung disease, but has the disadvantage of radiation exposure. Magnetic Resonance Imaging (MRI) is a radiation free alternative.To validate
Autor:
Leonie A, Tepper, Daan, Caudri, Elisabeth M W J, Utens, Els C, van der Wiel, Alexandra L, Quittner, Harm A W M, Tiddens
Publikováno v:
Pediatric pulmonology. 49(12)
Cystic fibrosis (CF) lung disease is characterized by bronchiectasis and trapped air on chest computed tomography (CT).We aim to validate bronchiectasis and trapped air as outcome measures by evaluating associations between changes in bronchiectasis,
Autor:
Aukje C. Bos, Els C. van der Wiel, Karla Gonzalez-Graniel, Leonie A. Tepper, Harm A.W.M. Tiddens, Hugo J. Duivenvoorden, Elisabeth M. W. J. Utens, Alexandra L. Quittner, Daan Caudri
Publikováno v:
European Respiratory Journal, 42, 371-379. European Respiratory Society
European respiratory journal, 42(2), 371-379. European Respiratory Society
European respiratory journal, 42(2), 371-379. European Respiratory Society
Cystic fibrosis (CF) is primarily characterised by bronchiectasis and trapped air on chest computed tomography (CT). The revised Cystic Fibrosis Questionnaire respiratory symptoms scale (CFQ-R RSS) measures health-related quality of life. To validate
Autor:
E. Van der Wiel, R.J.P. van der Valk, Daan Caudri, Alexandra L. Quittner, Elisabeth M. W. J. Utens, H.A.W.M. Tiddens, Leonie A. Tepper
Publikováno v:
Journal of Cystic Fibrosis. 11
An evaluation of the thyrotrophin-releasing hormone stimulation test in paediatric clinical practice
Publikováno v:
Hormone research. 69(1)
Aim: The aim of this retrospective study was to evaluate the clinical usefulness of the thyrotropin-releasing hormone (TRH) test in children with suspected hypothalamic or pituitary dysfunction. Methods: We reviewed the case notes of all patients in
Publikováno v:
Journal of Cystic Fibrosis. 12:S99
Objectives: For effective treatment of CF with inhaled drugs, efficient, easy to use devices are needed. This study was designed to assess time and practicability of Alpha-1-Antitrypsin (A1-PI(H)), (77mg/1.1ml) lung deposition in CF patients. Methods
Publikováno v:
European Radiology, 26(12), 4563-4569. Springer-Verlag
European Radiology
Tepper, L A, Caudri, D, Rovira, A P, Tiddens, H A W M & de Bruijne, M 2016, ' The development of bronchiectasis on chest computed tomography in children with cystic fibrosis : can pre-stages be identified? ', European Radiology, vol. 26, no. 12, pp. 4563-4569 . https://doi.org/10.1007/s00330-016-4329-z
European Radiology
Tepper, L A, Caudri, D, Rovira, A P, Tiddens, H A W M & de Bruijne, M 2016, ' The development of bronchiectasis on chest computed tomography in children with cystic fibrosis : can pre-stages be identified? ', European Radiology, vol. 26, no. 12, pp. 4563-4569 . https://doi.org/10.1007/s00330-016-4329-z
Objective Bronchiectasis is an important component of cystic fibrosis (CF) lung disease but little is known about its development. We aimed to study the development of bronchiectasis and identify determinants for rapid progression of bronchiectasis o