Zobrazeno 1 - 10
of 83
pro vyhledávání: '"H.-G. Posselt"'
Publikováno v:
Mycoses. 34:373-376
Mycological examination of sputum from 121 patients with cystic fibrosis by means of long-term cultures (4 weeks) revealed the occurrence of Candida albicans in low quantities in 70%, Aspergillus fumigatus in 30%, and Exophiala/Wangiella dermatitidis
Autor:
H.-G. Posselt, H. Schmidt
Publikováno v:
Radiologie up2date. 8:159-177
Cystic fibrosis (CF) is the most frequent metabolic disorder with autosomal recessive inheritance in the Caucasian population. The gene defect is located on the long arm of chromosome 7. In Germany today, the actual median survival is 37 years. The g
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 105:1739-1743
Autor:
Manfred Ballmann, Helge Hebestreit, Alexandra Hebestreit, S Rüdiger, Susi Kriemler, S. Junge, Thomas Schenk, H-G Posselt, Stephanie Kieser
Publikováno v:
European Respiratory Journal. 28:734-739
It is unclear whether a relationship between physical activity (PA) and maximal oxygen uptake (V'(O2,max)) exists in cystic fibrosis (CF) and, if so, whether the relationship reflects a direct effect or is mediated by the effects of confounding varia
Publikováno v:
Pneumologie. 56:542-546
Korperliches Training soll bei Patienten mit Cystischer Fibrose (CF) zu Leistungssteigerungen und zu einer Besserung der mukoziliaren Clearance fuhren. Ein regelmasiges Training wird jedoch haufig durch auftretende Infektionen und Zeitmangel eingesch
Publikováno v:
Pediatric Pulmonology. 31:13-16
SUMMARY. Continuous therapy with antistaphylococcal antibiotics is advocated by some cystic fibrosis (CF) centers, but it is unclear whether this strategy favors early colonization with P. aeruginosa. We used the data base for the German Centers of t
Autor:
William Meier-Ruge, L A Brunner, A M Holschneider, A. F. Schärli, G. Piket, H. G. Posselt, P Jordan, M Heminghaus, J Engert
Publikováno v:
European Journal of Pediatric Surgery. 9:67-74
Hypoganglionosis of the myenteric plexus of the colon is not clearly defined and seldom investigated. Colon segments from 15 children with an extended oligoeuronal hypoganglionosis up to the proximal resection end were morphometrically studied and co
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 25:317-320
Background: In 1994, first published reports described cystic fibrosis patients who experienced a then unknown complication-ileocecal and colonic stenoses with submucosal proliferation requiring surgical intervention. To investigate a suspected corre