-
2
-
-
0037460729
-
Cystic fibrosis
-
Ratjen F., and Doring G. Cystic fibrosis. Lancet 361 (2003) 681-689
-
(2003)
Lancet
, vol.361
, pp. 681-689
-
-
Ratjen, F.1
Doring, G.2
-
3
-
-
0029616734
-
Cystic fibrosis: genotypic and phenotypic variations
-
Zielenski J., and Tsui L.C. Cystic fibrosis: genotypic and phenotypic variations. Annu Rev Genet 29 (1995) 777-807
-
(1995)
Annu Rev Genet
, vol.29
, pp. 777-807
-
-
Zielenski, J.1
Tsui, L.C.2
-
4
-
-
0030473619
-
Genotype-phenotype correlation in cystic fibrosis
-
Kerem E., and Kerem B. Genotype-phenotype correlation in cystic fibrosis. Pediatr Pulmonol 22 (1996) 387-395
-
(1996)
Pediatr Pulmonol
, vol.22
, pp. 387-395
-
-
Kerem, E.1
Kerem, B.2
-
5
-
-
0031471090
-
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
-
Corey M., Edwards L., Levison H., and Knowles M. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis. J Pediatr 131 (1997) 809-814
-
(1997)
J Pediatr
, vol.131
, pp. 809-814
-
-
Corey, M.1
Edwards, L.2
Levison, H.3
Knowles, M.4
-
6
-
-
0037093814
-
Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients
-
Schluchter M.D., Konstan M.W., and Davis P.B. Jointly modelling the relationship between survival and pulmonary function in cystic fibrosis patients. Stat Med 21 (2002) 1271-1287
-
(2002)
Stat Med
, vol.21
, pp. 1271-1287
-
-
Schluchter, M.D.1
Konstan, M.W.2
Davis, P.B.3
-
8
-
-
0141956255
-
Allergic bronchopulmonary aspergillosis in cystic fibrosis - state of the art: Cystic Fibrosis Foundation Consensus Conference
-
Stevens D.A., Moss R.B., Kurup V.P., et al. Allergic bronchopulmonary aspergillosis in cystic fibrosis - state of the art: Cystic Fibrosis Foundation Consensus Conference. Clin Infect Dis 37 Suppl. 3 (2003) S225-S264
-
(2003)
Clin Infect Dis
, vol.37
, Issue.SUPPL. 3
-
-
Stevens, D.A.1
Moss, R.B.2
Kurup, V.P.3
-
9
-
-
0036063628
-
How useful is fecal pancreatic elastase 1 as a marker of exocrine pancreatic disease?
-
Beharry S., Ellis L., Corey M., Marcon M., and Durie P. How useful is fecal pancreatic elastase 1 as a marker of exocrine pancreatic disease?. J Pediatr 141 (2002) 84-90
-
(2002)
J Pediatr
, vol.141
, pp. 84-90
-
-
Beharry, S.1
Ellis, L.2
Corey, M.3
Marcon, M.4
Durie, P.5
-
10
-
-
0032783588
-
Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report
-
Moran A., Hardin D., Rodman D., et al. Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report. Diabetes Res Clin Pract 54 (1999) 61-73
-
(1999)
Diabetes Res Clin Pract
, vol.54
, pp. 61-73
-
-
Moran, A.1
Hardin, D.2
Rodman, D.3
-
11
-
-
0033773012
-
Consensus statement: antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus
-
Doring G., Conway S.P., Heijerman, et al. Consensus statement: antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis: a European consensus. Eur Respir J 16 (2000) 749-767
-
(2000)
Eur Respir J
, vol.16
, pp. 749-767
-
-
Doring, G.1
Conway, S.P.2
Heijerman3
-
12
-
-
0031955880
-
Circulating adhesion molecules in cystic fibrosis
-
De Rose V., Oliva A., Messore B., Grosso B., Mollar C., and Pozzi E. Circulating adhesion molecules in cystic fibrosis. Am J Respir Crit Care Med 157 (1998) 1234-1239
-
(1998)
Am J Respir Crit Care Med
, vol.157
, pp. 1234-1239
-
-
De Rose, V.1
Oliva, A.2
Messore, B.3
Grosso, B.4
Mollar, C.5
Pozzi, E.6
-
14
-
-
0029090616
-
Standardization of spirometry, 1994 update
-
American Thoracic Society. Standardization of spirometry, 1994 update. Am J Respir Crit Care Med 152 (1995) 1107-1136
-
(1995)
Am J Respir Crit Care Med
, vol.152
, pp. 1107-1136
-
-
American Thoracic Society1
-
15
-
-
19944433078
-
Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis
-
De Rose V., Arduino C., Cappello N., et al. Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis. Eur J Hum Genet 13 (2004) 96-101
-
(2004)
Eur J Hum Genet
, vol.13
, pp. 96-101
-
-
De Rose, V.1
Arduino, C.2
Cappello, N.3
-
16
-
-
33645704837
-
-
Stata Press, College Station, Texas, USA
-
Rabe-Hesketh S., and Skrondal A. Multilevel and longitudinal modeling using Stata-Cho 3-3 linear random-coefficient and growth-curve models (2005), Stata Press, College Station, Texas, USA
-
(2005)
Multilevel and longitudinal modeling using Stata-Cho 3-3 linear random-coefficient and growth-curve models
-
-
Rabe-Hesketh, S.1
Skrondal, A.2
-
18
-
-
0029016495
-
Gender difference in cystic fibrosis: Pseudomonas aeruginosa infection
-
Demko C.A., Byard P.J., and Davis P.B. Gender difference in cystic fibrosis: Pseudomonas aeruginosa infection. J Clin Epidemiol 48 (1995) 712-718
-
(1995)
J Clin Epidemiol
, vol.48
, pp. 712-718
-
-
Demko, C.A.1
Byard, P.J.2
Davis, P.B.3
-
19
-
-
0031021662
-
Identifying treatments that halt progression of pulmonary disease in cystic fibrosis
-
Davis P.B., Byard P.J., and Konstan M.W. Identifying treatments that halt progression of pulmonary disease in cystic fibrosis. Pediatr Res 41 (1997) 161-165
-
(1997)
Pediatr Res
, vol.41
, pp. 161-165
-
-
Davis, P.B.1
Byard, P.J.2
Konstan, M.W.3
-
20
-
-
0033827478
-
Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patients Registry
-
Zemel B.S., Jaward A.F., FitzSimmons S., and Stallings V.A. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patients Registry. J Pediatr 137 (2000) 374-380
-
(2000)
J Pediatr
, vol.137
, pp. 374-380
-
-
Zemel, B.S.1
Jaward, A.F.2
FitzSimmons, S.3
Stallings, V.A.4
-
21
-
-
0036311232
-
Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project
-
Steinkamp G., and Wiedemann B. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project. Thorax 57 (2002) 596-601
-
(2002)
Thorax
, vol.57
, pp. 596-601
-
-
Steinkamp, G.1
Wiedemann, B.2
-
22
-
-
0036112237
-
Predictor of deterioration of lung function in cystic fibrosis
-
Schaedel C., de Monestrol I., Hjelte L., et al. Predictor of deterioration of lung function in cystic fibrosis. Pediatr Pulmonol 33 (2002) 483-491
-
(2002)
Pediatr Pulmonol
, vol.33
, pp. 483-491
-
-
Schaedel, C.1
de Monestrol, I.2
Hjelte, L.3
-
23
-
-
0025013016
-
Effects of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients
-
Lewin L.O., Byard P.J., and Davis P.B. Effects of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients. J Clin Epidemiol 43 (1990) 125-131
-
(1990)
J Clin Epidemiol
, vol.43
, pp. 125-131
-
-
Lewin, L.O.1
Byard, P.J.2
Davis, P.B.3
-
24
-
-
0025355607
-
Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa
-
Kerem E., Corey M., Gold M., and Levison H. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa. J Pediatr 116 (1990) 1653-1658
-
(1990)
J Pediatr
, vol.116
, pp. 1653-1658
-
-
Kerem, E.1
Corey, M.2
Gold, M.3
Levison, H.4
-
25
-
-
33947263039
-
The relationship of clinical and inflammatory markers to outcome in stable patients with cystic fibrosis
-
Downey D.G., Martin S.L., Dempster M., et al. The relationship of clinical and inflammatory markers to outcome in stable patients with cystic fibrosis. Pediatr Pulmonol 42 (2007) 216-220
-
(2007)
Pediatr Pulmonol
, vol.42
, pp. 216-220
-
-
Downey, D.G.1
Martin, S.L.2
Dempster, M.3
-
26
-
-
34447530328
-
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
-
Konstan M.J., Morgan W.J., Butler S.M., et al. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr 151 (2007) 134-139
-
(2007)
J Pediatr
, vol.151
, pp. 134-139
-
-
Konstan, M.J.1
Morgan, W.J.2
Butler, S.M.3
-
27
-
-
36348949002
-
Factors associated with lung function decline in adult patients with stable non-cystic fibrosis bronchiectasis
-
Martinez-Garcia M.A., Soler-Cataluna J.J., Perpina-Tordera M., Roman-Sanchez P., and Soriano J. Factors associated with lung function decline in adult patients with stable non-cystic fibrosis bronchiectasis. Chest 132 (2007) 1565-1572
-
(2007)
Chest
, vol.132
, pp. 1565-1572
-
-
Martinez-Garcia, M.A.1
Soler-Cataluna, J.J.2
Perpina-Tordera, M.3
Roman-Sanchez, P.4
Soriano, J.5
-
28
-
-
12144266591
-
One-year outcome after severe pulmonary exacerbation in adults with cystic fibrosis
-
Ellaffi M., Vinsonneau C., Coste J., et al. One-year outcome after severe pulmonary exacerbation in adults with cystic fibrosis. Am J Respir Crit Care Med 171 (2005) 158-164
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 158-164
-
-
Ellaffi, M.1
Vinsonneau, C.2
Coste, J.3
-
29
-
-
33344468629
-
Cystic fibrosis pulmonary exacerbations
-
Ferkol T., Rosenfeld M., and Milla C.E. Cystic fibrosis pulmonary exacerbations. J Pediatr 148 (2006) 259-264
-
(2006)
J Pediatr
, vol.148
, pp. 259-264
-
-
Ferkol, T.1
Rosenfeld, M.2
Milla, C.E.3
-
30
-
-
0036175259
-
Mechanisms and markers of airways inflammation in cystic fibrosis
-
De Rose V. Mechanisms and markers of airways inflammation in cystic fibrosis. Eur Respir J 19 (2002) 333-340
-
(2002)
Eur Respir J
, vol.19
, pp. 333-340
-
-
De Rose, V.1
-
31
-
-
34547731349
-
The effect of treatment of cystic fibrosis pulmonary exacerbations on airways and systemic inflammation
-
Downey D.G., Brockbank S., Martin L., Ennis M., and Elborn J.S. The effect of treatment of cystic fibrosis pulmonary exacerbations on airways and systemic inflammation. Pediatr Pulmonol 42 (2007) 729-735
-
(2007)
Pediatr Pulmonol
, vol.42
, pp. 729-735
-
-
Downey, D.G.1
Brockbank, S.2
Martin, L.3
Ennis, M.4
Elborn, J.S.5
-
32
-
-
0034066416
-
Airflow obstruction in bronchiectasis: correlation between computed tomography features and pulmonary function tests
-
Roberts H.R., Wells A.U., Milne D.G., et al. Airflow obstruction in bronchiectasis: correlation between computed tomography features and pulmonary function tests. Thorax 55 (2000) 198-204
-
(2000)
Thorax
, vol.55
, pp. 198-204
-
-
Roberts, H.R.1
Wells, A.U.2
Milne, D.G.3
-
33
-
-
0347766074
-
Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis
-
de Jong P.A., Nakano Y., Lequin M.H., et al. Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis. Eur Respir J 23 (2004) 93-97
-
(2004)
Eur Respir J
, vol.23
, pp. 93-97
-
-
de Jong, P.A.1
Nakano, Y.2
Lequin, M.H.3
-
34
-
-
34748882395
-
Dissociation of lung function, dyspnea ratings and pulmonary extension in bronchiectasis
-
Martinez-Garcia M.A., Perpina-Tordera M., Soler-Cataluna J.J., Roman-Sanchez P., Lloris-Bayo A., and Gonzales-Molina A. Dissociation of lung function, dyspnea ratings and pulmonary extension in bronchiectasis. Respir Med 101 (2007) 2248-2253
-
(2007)
Respir Med
, vol.101
, pp. 2248-2253
-
-
Martinez-Garcia, M.A.1
Perpina-Tordera, M.2
Soler-Cataluna, J.J.3
Roman-Sanchez, P.4
Lloris-Bayo, A.5
Gonzales-Molina, A.6
-
35
-
-
0034891408
-
Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF
-
Navarro J., Rainisio M., Harms H.K., et al. Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF. Eur Respir J 18 (2001) 298-305
-
(2001)
Eur Respir J
, vol.18
, pp. 298-305
-
-
Navarro, J.1
Rainisio, M.2
Harms, H.K.3
-
36
-
-
0027991656
-
Diabetes mellitus in cystic fibrosis: effects of insulin therapy on lung function and infections
-
Lanng S., Thorsteinsson B., Nerup J., and Koch C. Diabetes mellitus in cystic fibrosis: effects of insulin therapy on lung function and infections. Acta Pediatr 83 (1994) 849-853
-
(1994)
Acta Pediatr
, vol.83
, pp. 849-853
-
-
Lanng, S.1
Thorsteinsson, B.2
Nerup, J.3
Koch, C.4
-
37
-
-
0026635730
-
Influence of the development of diabetes mellitus on clinical status in patients with cystic fibrosis
-
Lanng S., Thorsteinson B., Nerup J., and Koch C. Influence of the development of diabetes mellitus on clinical status in patients with cystic fibrosis. Eur J Pediatr 151 (1992) 684-687
-
(1992)
Eur J Pediatr
, vol.151
, pp. 684-687
-
-
Lanng, S.1
Thorsteinson, B.2
Nerup, J.3
Koch, C.4
-
38
-
-
0034759112
-
Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: data from the European Epidemiologic Registry of cystic fibrosis
-
Koch C., Rainisio M., Madessani U., et al. Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: data from the European Epidemiologic Registry of cystic fibrosis. Pediatr Pulmonol 32 (2001) 343-350
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 343-350
-
-
Koch, C.1
Rainisio, M.2
Madessani, U.3
|