The Canadian Cystic Fibrosis Foundation ended 2010 with one of the year's more interesting collaborations between nonprofit organizations and commercial drug developers.
Dr. Stephenson's paper is based on data of about 5,000 patients in
the Canadian Cystic Fibrosis Registry, of which she is the director.
The study, funded by the U.S. Cystic Fibrosis Foundation, used data from 37,772 patients in the U.S. Cystic Fibrosis Foundation Registry and 5,149 patients in
the Canadian Cystic Fibrosis Registry.
The study was funded by the U.S. Cystic Fibrosis Foundation using data from 45,456 patients in the U.S. Cystic Fibrosis Foundation Registry and 5,941 patients in
the Canadian Cystic Fibrosis Registry from 1990 to 2013.
Not exact matches
Newborn screening for
cystic fibrosis is now available in seven
Canadian provinces.
Canadians with
cystic fibrosis were exposed to a high fat diet in the 1970s, which was not implemented in the United States until the 1980s.
«
Canadians with
cystic fibrosis living 20 years longer than they did 2 decades ago.»
Canadian guidelines for CF clinical care have been developed and are being published by
Cystic Fibrosis Canada.