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PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, p. e54521
Journal Article
Swiss medical weekly, ISSN 1424-7860, 01/2019, Volume 149
Primary ciliary dyskinesia (PCD) is a rare, hereditary, multiorgan disease caused by defects in the structure and function of motile cilia. It results in a... 
orphan diseases | epidemiology | patient registry | Swiss Primary Ciliary Dyskinesia Registry | primary ciliary dyskinesia | DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | DEFECTS | AGE
Journal Article
Pediatric Pulmonology, ISSN 8755-6863, 08/2019, Volume 54, Issue 8, pp. 1156 - 1161
Introduction The contribution of clinical investigations to prediction of long‐term outcomes of children investigated for asthma is unclear. Aim We performed a... 
epidemiology | cohort | asthma | respiratory | wheeze | prognosis | BRONCHIAL RESPONSIVENESS | PERSISTENCE | MANNITOL DRY POWDER | CHILDHOOD ASTHMA | CHILDREN | CHALLENGE | RESPIRATORY SYSTEM | EXACERBATIONS | PEDIATRICS | EXHALED NITRIC-OXIDE | ASSOCIATION | AGE | Pediatrics | Pets | Allergy | Wheeze | Clinics | Asthma in children | Nitric oxide | Epidemiology | Investigations | Testing
Journal Article
PloS one, 2013, Volume 8, Issue 1, p. e54521
Fractional exhaled nitric oxide (FENO), a non-invasive marker of eosinophilic airway inflammation, is increasingly used for diagnostic and therapeutic... 
Asthma - diagnosis | Dry Powder Inhalers | Pneumonia - physiopathology | Asthma - physiopathology | Humans | Breath Tests | Male | Asthma - drug therapy | Pneumonia - drug therapy | Asthma - complications | Mannitol - administration & dosage | Pneumonia - diagnosis | Adolescent | Pneumonia - complications | Female | Exhalation | Nitric Oxide - metabolism | Child
Journal Article
Pediatric Pulmonology, ISSN 8755-6863, 03/2019, Volume 54, Issue 3, pp. 264 - 272
Objectives In the national newborn screening programme for CF in Switzerland, we compared the performance of two sweat test methods, by investigating the... 
chloride measurement | conductivity | sweat test | newborn screening | cystic fibrosis | MANAGEMENT | MACRODUCT | PERFORMANCE | CHILDREN | ANALYZER | SCREEN | RESPIRATORY SYSTEM | INFANTS | PEDIATRICS | EVIDENCE-BASED GUIDELINES | Infants (Newborn) | Gene mutations | Testing equipment | Cystic fibrosis | Diagnosis | Comparative analysis | Electric properties
Journal Article
SWISS MEDICAL WEEKLY, ISSN 1424-7860, 06/2019, Volume 149, p. w20081
Congenital lung anomalies are a group of rare malformations, often diagnosed during the prenatal period. Guidelines on how to manage these patients are... 
POSTNATAL MANAGEMENT | MULTICENTER | RESECTION | CLASSIFICATION | congenital lung anomalies | rare diseases | SEQUESTRATION | MEDICINE, GENERAL & INTERNAL | database | CYSTIC ADENOMATOID MALFORMATION | DISEASE | PULMONARY AIRWAY MALFORMATION | OUTCOMES | biobank
Journal Article
European Respiratory Journal, ISSN 0903-1936, 09/2015, Volume 46, Issue 3, pp. 601 - 603
Journal Article
The European respiratory journal, 09/2019
There are little data on the usefulness of different tests to diagnose asthma in children. We assessed the contribution of a detailed history and a variety of... 
Journal Article
DEUTSCHES ARZTEBLATT INTERNATIONAL, ISSN 1866-0452, 05/2013, Volume 110, Issue 20, pp. 356 - U25
Background: From January 2011 onward, the Swiss newborn screening (NBS) program has included a test for cystic fibrosis (CF). In this study, we evaluate the... 
CONSENSUS | DIAGNOSIS | MEDICINE, GENERAL & INTERNAL | GUIDELINES | INFANTS | CHILDREN | Original
Journal Article
Journal Article
Deutsches Arzteblatt International, ISSN 1866-0452, 05/2013, Volume 110, Issue 20, pp. 356 - 363
Journal Article
Pediatric Pulmonology, ISSN 8755-6863, 04/2014, Volume 49, Issue 4, pp. 342 - 347
Journal Article