Background In 1992 France set up a national cystic fibrosis observatory (Observatoire national de la mucoviscidose, ONM) to monitor the state of health of patients on an annual basis. Using the ONM data, this study estimates the main indicators for life expectancy and assesses the total number of cystic fibrosis patients. Methods The data for the years 1994 to 2003 are divided into 3-year periods. Life tables are drawn up for these periods, from which mean and median lengths of life are determined. Using the most recent life table, the number of births in 2003 and the incidence of the disease, the total population of patients can be estimated, assuming a stationary population. Results In 2001–2003, life expectancy at birth of patients reg...
Background Country-specific patients' registries are rarely used to make international comparisons b...
Background: Survival in cystic fibrosis (CF) has progressively improved and the female-gender disadv...
Data collected in the European Cystic Fibrosis Society Patient Registry (ECFSPR) database were used ...
AbstractBackgroundIn 1992 France set up a national cystic fibrosis observatory (Observatoire nationa...
ObjectivesIn 1992, the medical Council of the association Vaincre la Mucoviscidose, set up a nationa...
International audienceABSTRACT: BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder ...
Objectives In 1992, the medical Council of the association Vaincre la Mucoviscidose, set up a nation...
The aim of this study is to analyze population-based mortality attributed to cystic fibrosis (CF) ov...
Median survival has increased in people with cystic fibrosis (CF) during the past six decades, which...
Background—The UK has published ob-served cohort survival figures for subjects with cystic fibrosis ...
Abstract-This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through th...
Objective: To analyze mortality trends among people who died with a diagnosis of cystic fibrosis fr...
Abstract Background Cystic fibrosis (CF) is an autosomal recessive disorder whose incidence has long...
SUMMARY Life tables were calculated for 273 British children with cystic fibrosis for the period 197...
This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through this system...
Background Country-specific patients' registries are rarely used to make international comparisons b...
Background: Survival in cystic fibrosis (CF) has progressively improved and the female-gender disadv...
Data collected in the European Cystic Fibrosis Society Patient Registry (ECFSPR) database were used ...
AbstractBackgroundIn 1992 France set up a national cystic fibrosis observatory (Observatoire nationa...
ObjectivesIn 1992, the medical Council of the association Vaincre la Mucoviscidose, set up a nationa...
International audienceABSTRACT: BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder ...
Objectives In 1992, the medical Council of the association Vaincre la Mucoviscidose, set up a nation...
The aim of this study is to analyze population-based mortality attributed to cystic fibrosis (CF) ov...
Median survival has increased in people with cystic fibrosis (CF) during the past six decades, which...
Background—The UK has published ob-served cohort survival figures for subjects with cystic fibrosis ...
Abstract-This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through th...
Objective: To analyze mortality trends among people who died with a diagnosis of cystic fibrosis fr...
Abstract Background Cystic fibrosis (CF) is an autosomal recessive disorder whose incidence has long...
SUMMARY Life tables were calculated for 273 British children with cystic fibrosis for the period 197...
This paper describes the Data Registry System of the Cystic Fibrosis Foundation. Through this system...
Background Country-specific patients' registries are rarely used to make international comparisons b...
Background: Survival in cystic fibrosis (CF) has progressively improved and the female-gender disadv...
Data collected in the European Cystic Fibrosis Society Patient Registry (ECFSPR) database were used ...