A standardized approach to estimating survival statistics for population-based cystic fibrosis registry cohorts.

[1]  G. A. Whitmore,et al.  A contemporary survival analysis of individuals with cystic fibrosis: a cohort study , 2014, European Respiratory Journal.

[2]  H. Quinton,et al.  Validation and use of a parametric model for projecting cystic fibrosis survivorship beyond observed data: a birth cohort analysis , 2011, Thorax.

[3]  J. Nick,et al.  Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis. , 2010, American journal of respiratory and critical care medicine.

[4]  Anil Mehta,et al.  Comparative analysis of Cystic Fibrosis Registry data from the UK with USA, France and Australasia. , 2005, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[5]  M. Kosorok,et al.  Comparison of growth status of patients with cystic fibrosis between the United States and Canada. , 1999, The American journal of clinical nutrition.

[6]  Chiang Cl Variance and covariance of life table functions estimated from a sample of deaths. , 1967, Vital and health statistics. Series 2, Data evaluation and methods research.

[7]  H. Quinton,et al.  The application of current lifetable methods to compare cystic fibrosis median survival internationally is limited. , 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

[8]  Paul C Lambert,et al.  Providing more up-to-date estimates of patient survival: a comparison of standard survival analysis with period analysis using life-table methods and proportional hazards models. , 2004, Journal of clinical epidemiology.

[9]  M. Corey,et al.  A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. , 1988, Journal of clinical epidemiology.