Sökning: "cystic fibrosis"

Visar resultat 21 - 25 av 89 avhandlingar innehållade orden cystic fibrosis.

1. 21. Monitoring cystic fibrosis lung disease in children - Clinical utility and associations between functional and structural methods

   Författare :Marcus Svedberg; Göteborgs universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; cystic fibrosis; children; lung disease;

   Sammanfattning : Background: Cystic Fibrosis (CF) is an inherited progressive disease that causes severe damage to the airways and other organs of the body. Many methods are available to track CF lung disease but longitudinal data are needed to better understand the clinical utility and associations between different methods. LÄS MER

3. 22. Chest Tomosynthesis for Detection and Surveillance of Pulmonary Pathology. Studies on Cystic Fibrosis and Solid Pulmonary Nodules

   Författare :Carin Meltzer; Göteborgs universitet; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; digital tomosynthesis; cystic fibrosis; solid lung nodules;

   Sammanfattning : Introduction: Digital tomosynthesis (DTS) is a relatively new imaging modality in thoracic imaging. The technique is based on the equipment of conventional radiography, upgraded with a moving tube that enables separation of structures that are superimposed on chest x-ray (CXR). LÄS MER

4. 23. Non invasive ventilation in people with cystic fibrosis

   Författare :Cecilia Rodriguez Hortal; Karolinska Institutet; Karolinska Institutet; []
   Nyckelord :;

   Sammanfattning : Background: Cystic fibrosis (CF) is the most common life shortening autosomal recessive inherited disease affecting Caucasian people. The two main clinical characteristics of CF are progressive pulmonary disease and pancreatic insufficiency. The goal of airway clearance technique (ACT) is to improve ventilation and mucociliary clearance. LÄS MER

5. 24. Exocrine glands in animal models for cystic fibrosis : X-ray microanalysis and morphological, physiological and biochemical studies

   Författare :R. Margareta Müller; Stockholms universitet; []
   Nyckelord :NATURVETENSKAP; NATURAL SCIENCES;

   Sammanfattning : .... LÄS MER

7. 25. On Mechanisms Impairing Airway Host Defence in Cystic Fibrosis

   Författare :Sandra Jovic; allergologi och palliativ medicin Lungmedicin; []
   Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES;

   Sammanfattning : Cystic fibrosis is an inherited disease, caused by mutations of the cystic fibrosis transmembrane conductance regulator gene. The gene codes for a protein that serve as chloride channel. In cystic fibrosis, this protein is lacking or has a defect function resulting in a thick and sticky mucus of the airways. LÄS MER