-
1
-
-
33847711906
-
Cystic fibrosis mortality and survival in the UK: 1947-2003
-
Dodge JA, Lewis PA, Stanton M, et al. Cystic fibrosis mortality and survival in the UK: 1947-2003. Eur Respir J 2007; 29: 522-526.
-
(2007)
Eur Respir J
, vol.29
, pp. 522-526
-
-
Dodge, J.A.1
Lewis, P.A.2
Stanton, M.3
-
2
-
-
0032513942
-
Clinical outcome in relation to care in centres specialising in cystic fibrosis: Cross sectional study
-
Mahadeva R, Webb K, Westerbeek RC, et al. Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study. BMJ 1998; 316: 1771-1775.
-
(1998)
BMJ
, vol.316
, pp. 1771-1775
-
-
Mahadeva, R.1
Webb, K.2
Westerbeek, R.C.3
-
3
-
-
0029924585
-
Determinants of mortality from cystic fibrosis in Canada, 1970-1989
-
Corey M, Farewell V. Determinants of mortality from cystic fibrosis in Canada, 1970-1989. Am J Epidemiol 1996; 143: 1007-1017.
-
(1996)
Am J Epidemiol
, vol.143
, pp. 1007-1017
-
-
Corey, M.1
Farewell, V.2
-
4
-
-
0034784660
-
Cystic fibrosis: Review of the decade
-
Jaffe A, Bush A. Cystic fibrosis: review of the decade. Monaldi Arch Chest Dis 2001; 56: 240-247.
-
(2001)
Monaldi Arch Chest Dis
, vol.56
, pp. 240-247
-
-
Jaffe, A.1
Bush, A.2
-
5
-
-
33745809841
-
Cystic fibrosis: Terminology and diagnostic algorithms
-
De Boeck K, Wilschanski M, Castellani C, et al. Cystic fibrosis: terminology and diagnostic algorithms. Thorax 2006; 61: 627-635.
-
(2006)
Thorax
, vol.61
, pp. 627-635
-
-
De Boeck, K.1
Wilschanski, M.2
Castellani, C.3
-
6
-
-
60649115622
-
Growing old with cystic fibrosis: The characteristics of long-term survivors of cystic fibrosis
-
Simmonds NJ, Cullinan P, Hodson ME. Growing old with cystic fibrosis: the characteristics of long-term survivors of cystic fibrosis. Respir Med 2008; 103: 629-635.
-
(2008)
Respir Med
, vol.103
, pp. 629-635
-
-
Simmonds, N.J.1
Cullinan, P.2
Hodson, M.E.3
-
7
-
-
55549136375
-
An international/ multicentre report on patients with cystic fibrosis (CF) over the age of 40 years
-
Hodson ME, Simmonds NJ, Warwick WJ, et al. An international/ multicentre report on patients with cystic fibrosis (CF) over the age of 40 years. J Cyst Fibros 2008; 7: 537-542.
-
(2008)
J Cyst Fibros
, vol.7
, pp. 537-542
-
-
Hodson, M.E.1
Simmonds, N.J.2
Warwick, W.J.3
-
8
-
-
25844491194
-
Genetic modifiers of lung disease in cystic fibrosis
-
Drumm ML, Konstan MW, Schluchter MD, et al. Genetic modifiers of lung disease in cystic fibrosis. N Engl J Med 2005; 353: 1443-1453.
-
(2005)
N Engl J Med
, vol.353
, pp. 1443-1453
-
-
Drumm, M.L.1
Konstan, M.W.2
Schluchter, M.D.3
-
9
-
-
0347812925
-
Non-genetic influences on cystic fibrosis lung disease: The role of sociodemographic characteristics, environmental exposures, and healthcare interventions
-
Schechter MS. Non-genetic influences on cystic fibrosis lung disease: the role of sociodemographic characteristics, environmental exposures, and healthcare interventions. Semin Respir Crit Care Med 2003; 24: 639-652.
-
(2003)
Semin Respir Crit Care Med
, vol.24
, pp. 639-652
-
-
Schechter, M.S.1
-
10
-
-
27644508698
-
Manifestations of cystic fibrosis diagnosed in adulthood
-
Nick JA, Rodman DM. Manifestations of cystic fibrosis diagnosed in adulthood. Curr Opin Pulm Med 2005; 11: 513-518.
-
(2005)
Curr Opin Pulm Med
, vol.11
, pp. 513-518
-
-
Nick, J.A.1
Rodman, D.M.2
-
11
-
-
20144385873
-
Late diagnosis defines a unique population of long-term survivors of cystic fibrosis
-
Rodman DM, Polis JM, Heltshe SL, et al. Late diagnosis defines a unique population of long-term survivors of cystic fibrosis. Am J Respir Crit Care Med 2005; 171: 621-626.
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 621-626
-
-
Rodman, D.M.1
Polis, J.M.2
Heltshe, S.L.3
-
12
-
-
0031916045
-
Relationship between socioeconomic status and disease severity in cystic fibrosis
-
Schechter MS, Margolis PA. Relationship between socioeconomic status and disease severity in cystic fibrosis. J Pediatr 1998; 132: 260-264.
-
(1998)
J Pediatr
, vol.132
, pp. 260-264
-
-
Schechter, M.S.1
Margolis, P.A.2
-
13
-
-
0034987271
-
The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States
-
Schechter MS, Shelton BJ, Margolis PA, et al. The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States. Am J Respir Crit Care Med 2001; 163: 1331-1337.
-
(2001)
Am J Respir Crit Care Med
, vol.163
, pp. 1331-1337
-
-
Schechter, M.S.1
Shelton, B.J.2
Margolis, P.A.3
-
14
-
-
0024590336
-
Effects of social class, sex, and region of residence on age at death from cystic fibrosis
-
Britton JR. Effects of social class, sex, and region of residence on age at death from cystic fibrosis. BMJ 1989; 298: 483-487.
-
(1989)
BMJ
, vol.298
, pp. 483-487
-
-
Britton, J.R.1
-
15
-
-
0017843165
-
Relative underweight in cystic fibrosis and its prognostic value
-
Kraemer R, Rudeberg A, Hadorn B, et al. Relative underweight in cystic fibrosis and its prognostic value. Acta Paediatr Scand 1978; 67: 33-37.
-
(1978)
Acta Paediatr Scand
, vol.67
, pp. 33-37
-
-
Kraemer, R.1
Rudeberg, A.2
Hadorn, B.3
-
16
-
-
0023923679
-
A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto
-
Corey M, McLaughlin FJ, Williams M, et al. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1988; 41: 583-591.
-
(1988)
J Clin Epidemiol
, vol.41
, pp. 583-591
-
-
Corey, M.1
McLaughlin, F.J.2
Williams, M.3
-
17
-
-
0023639146
-
Clinical features, survival rate, and prognostic factors in young adults with cystic fibrosis
-
Huang NN, Schidlow DV, Szatrowski TH, et al. Clinical features, survival rate, and prognostic factors in young adults with cystic fibrosis. Am J Med 1987; 82: 871-879.
-
(1987)
Am J Med
, vol.82
, pp. 871-879
-
-
Huang, N.N.1
Schidlow, D.V.2
Szatrowski, T.H.3
-
18
-
-
34249864458
-
Predictors of mortality in adults with cystic fibrosis
-
Courtney JM, Bradley J, Mccaughan J, et al. Predictors of mortality in adults with cystic fibrosis. Pediatr Pulmonol 2007; 42: 525-532.
-
(2007)
Pediatr Pulmonol
, vol.42
, pp. 525-532
-
-
Courtney, J.M.1
Bradley, J.2
Mccaughan, J.3
-
19
-
-
1542267792
-
Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis
-
Lai HJ, Cheng Y, Cho H, et al. Association between initial disease presentation, lung disease outcomes, and survival in patients with cystic fibrosis. Am J Epidemiol 2004; 159: 537-546.
-
(2004)
Am J Epidemiol
, vol.159
, pp. 537-546
-
-
Lai, H.J.1
Cheng, Y.2
Cho, H.3
-
21
-
-
27144501047
-
Is there still a gender gap in cystic fibrosis?
-
Verma N, Bush A, Buchdahl R. Is there still a gender gap in cystic fibrosis? Chest 2005; 128: 2824-2834.
-
(2005)
Chest
, vol.128
, pp. 2824-2834
-
-
Verma, N.1
Bush, A.2
Buchdahl, R.3
-
22
-
-
0036320272
-
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
-
Emerson J, Rosenfeld M, McNamara S, et al. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002; 34: 91-100.
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 91-100
-
-
Emerson, J.1
Rosenfeld, M.2
McNamara, S.3
-
23
-
-
0026831341
-
Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis
-
Henry RL, Mellis CM, Petrovic L. Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis. Pediatr Pulmonol 1992; 12: 158-161.
-
(1992)
Pediatr Pulmonol
, vol.12
, pp. 158-161
-
-
Henry, R.L.1
Mellis, C.M.2
Petrovic, L.3
-
24
-
-
23744479518
-
Massive hemoptysis in cystic fibrosis
-
Flume PA, Yankaskas JR, Ebeling M, et al. Massive hemoptysis in cystic fibrosis. Chest 2005; 128: 729-738.
-
(2005)
Chest
, vol.128
, pp. 729-738
-
-
Flume, P.A.1
Yankaskas, J.R.2
Ebeling, M.3
-
25
-
-
0028011754
-
C-reactive protein is not a useful indicator of intermittent bacterial colonization in early lung disease of patients with cystic fibrosis
-
Watkin SL, Elborn JS, Cordon SM, et al. C-reactive protein is not a useful indicator of intermittent bacterial colonization in early lung disease of patients with cystic fibrosis. Pediatr Pulmonol 1994; 17: 6-10.
-
(1994)
Pediatr Pulmonol
, vol.17
, pp. 6-10
-
-
Watkin, S.L.1
Elborn, J.S.2
Cordon, S.M.3
-
26
-
-
0034891408
-
Factors associated with poor pulmonary function: Cross-sectional analysis of data from the ERCF. European Epidemiologic Registry of Cystic Fibrosis
-
Navarro J, Rainisio M, Harms HK, et al. Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF. European Epidemiologic Registry of Cystic Fibrosis. Eur Respir J 2001; 18: 298-305.
-
(2001)
Eur Respir J
, vol.18
, pp. 298-305
-
-
Navarro, J.1
Rainisio, M.2
Harms, H.K.3
-
28
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem B, Rommens JM, Buchanan JA, et al. Identification of the cystic fibrosis gene: genetic analysis. Science 1989; 245: 1073-1080. (Pubitemid 19231815)
-
(1989)
Science
, vol.245
, Issue.4922
, pp. 1073-1080
-
-
Kerem, B.-S.1
Rommens, J.M.2
Buchanan, J.A.3
Markiewicz, D.4
Cox, T.K.5
Chakravarti, A.6
Buchwald, M.7
Tsui, L.-C.8
-
29
-
-
67651159527
-
-
UK Cystic Fibrosis Database. University of Dundee Date last accessed: October 4, 2010. Date last updated: April, 2: 2010
-
UK Cystic Fibrosis Database. Annual Data Report 2004. University of Dundee 2006. www.cystic-fibrosis.org.uk/pdfs/annualreport/AuditReport2004.pdf Date last accessed: October 4, 2010. Date last updated: April, 2: 2010.
-
(2006)
Annual Data Report 2004
-
-
-
30
-
-
0021340634
-
Pseudomonas cepacia infection in cystic fibrosis: An emerging problem
-
Isles A, Maclusky I, Corey M, et al. Pseudomonas cepacia infection in cystic fibrosis: an emerging problem. J Pediatr 1984; 104: 206-210.
-
(1984)
J Pediatr
, vol.104
, pp. 206-210
-
-
Isles, A.1
Maclusky, I.2
Corey, M.3
|