Updated: 07 Jan 2001
1 Kps. enth.: Tanninalbuminat 250 mg.
Cystic fibrosis (CF) is a genetic condition caused by a defect in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel. The Cystic Fibrosis Knowledge Centre provides healthcare professionals with access to disease awareness information, emerging and established treatment options and current best practice based on recently updated guidelines by the European Cystic Fibrosis Society (ECFS). A resources section contains external links to upcoming medical conferences and patient support groups.
This resource is developed by EPG Health Media for epgonline.org, supported by an independent educational grant from Vertex.
This European Obesity Initiative CME series contains three online modules, which are ideal for healthcare professionals looking to widen their understanding of obesity as a serious medical illness. Each module is EACCME-accredited and free to complete. Successful completion of the series will earn participants a combined total of 5 European CME credits (ECMECs).
Gelatine, Farbstoffe E 171, E 172.
Zus.: 1 Tbl. enth.: Tanninalbuminat 500 mg.
Weit. Bestandteile: Gelatine, hochdisperses Siliciumdioxid, Stearinsäure.
Überempfindlichkeit gegenüber Ovalbuminanteil.
Strenge Ind.-Stellung in den ersten 3 Mon. Gr 2 .
See disease awareness facts and stats, information on sebelipase alfa (the first and only licensed treatment for LAL-D) and resources section, including expert video channel…