Zobrazeno 1 - 10
of 60
pro vyhledávání: '"W. Wiebicke"'
Publikováno v:
Atemwegs- und Lungenkrankheiten. 38:381-384
Publikováno v:
European Journal of Pediatrics. 155:603-607
Publikováno v:
Klinische Pädiatrie. 212:41-43
(mutation D110H). We report the history of an infant who presented with hypotonic dehydration and metabolic alkalosis, in whom the diagnosis of cystic fibrosis was made on the basis of investigations for rare cystic fibrosis mutations. Since no other
Publikováno v:
Klinische Padiatrie. 212(1)
We report the history of an infant who presented with hypotonic dehydration and metabolic alkalosis, in whom the diagnosis of cystic fibrosis was made on the basis of investigations for rare cystic fibrosis mutations. Since no other signs and symptom
Autor:
W. Wiebicke
Publikováno v:
Nasale Maskenbeatmung im Kindes-und Erwachsenenalter ISBN: 9783540631545
We report the history of a male patient with cystic fibrosis (homozygous for the delta F508 mutation) who developed life-threatening respiratory failure due to his advanced lung disease at the age of 26 years. Intermittent positive pressure via nasal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b749ebf6820f1786e58289a0f5bea3aa
https://doi.org/10.1007/978-3-642-60853-7_2
https://doi.org/10.1007/978-3-642-60853-7_2
Publikováno v:
European journal of pediatrics. 152(8)
We report a 10-month-old male infant who was admitted to our hospital with a history of failure to thrive and bulky stools. On examination, he was dystrophic and had a protruding abdomen, but he was well oxygenated and his lungs were clear on auscult
Autor:
W, Wiebicke
Publikováno v:
Pneumologie (Stuttgart, Germany). 46(11)
Publikováno v:
Pediatric pulmonology. 13(2)
Bacterial colonization of the tracheo-bronchial tree is common and an established risk factor for infection in ventilated newborns. Elastase, a highly active proteinase, and lactoferrin, an iron-binding protein and potential modulator of the inflamma
Publikováno v:
Pneumologie (Stuttgart, Germany). 45(11)
We report a 13-year old boy with a chronic pseudomonas bronchitis who was first diagnosed as having cystic fibrosis at this age because of an elevated sweat chloride employing pilocarpine-iontophoresis. He is heterozygote for the gene mutation Delta
Autor:
W, Wiebicke, J, Seidenberg
Publikováno v:
Pneumologie (Stuttgart, Germany). 44(10)
We report the complex clinical course over 15 years in a child who at the age of 19 months developed patchy pneumonic infiltrates and bronchiolitis after measles. Chronic atelectasis led to resection of the right upper lung lobe. He developed bilater