-
1
-
-
0000471085
-
Cystic fibrosis of the pancreas and its relation to celiac disease. A clinical and pathological study
-
Anderson D.H. Cystic fibrosis of the pancreas and its relation to celiac disease. A clinical and pathological study. Arch Dis Child 56 (1938) 344-399
-
(1938)
Arch Dis Child
, vol.56
, pp. 344-399
-
-
Anderson, D.H.1
-
3
-
-
33847711906
-
Cystic fibrosis mortality and survival in the UK: 1947-2003
-
Dodge J.A., Lewis P.A., Stanton M., and Wilsher J. Cystic fibrosis mortality and survival in the UK: 1947-2003. Eur Respir J 29 (2007) 522-526
-
(2007)
Eur Respir J
, vol.29
, pp. 522-526
-
-
Dodge, J.A.1
Lewis, P.A.2
Stanton, M.3
Wilsher, J.4
-
5
-
-
0347812925
-
Non-genetic influences on cystic fibrosis lung disease: the role of sociodemographic characteristics, environmental exposures, and healthcare interventions
-
Schechter M.S. Non-genetic influences on cystic fibrosis lung disease: the role of sociodemographic characteristics, environmental exposures, and healthcare interventions. Semin Respir Crit Care Med 24 (2003) 639-652
-
(2003)
Semin Respir Crit Care Med
, vol.24
, pp. 639-652
-
-
Schechter, M.S.1
-
6
-
-
33745809841
-
Cystic fibrosis: terminology and diagnostic algorithms
-
De Boeck K., Wilschanski M., Castellani C., et al. Cystic fibrosis: terminology and diagnostic algorithms. Thorax 61 (2006) 627-635
-
(2006)
Thorax
, vol.61
, pp. 627-635
-
-
De Boeck, K.1
Wilschanski, M.2
Castellani, C.3
-
7
-
-
0033870680
-
Health status and sociodemographic characteristics of adults receiving a cystic fibrosis diagnosis after age 18 years
-
Widerman E., Millner L., Sexauer W., and Fiel S. Health status and sociodemographic characteristics of adults receiving a cystic fibrosis diagnosis after age 18 years. Chest 118 (2000) 427-433
-
(2000)
Chest
, vol.118
, pp. 427-433
-
-
Widerman, E.1
Millner, L.2
Sexauer, W.3
Fiel, S.4
-
8
-
-
6344231597
-
Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood
-
Gilljam M., Ellis L., Corey M., Zielenski J., Durie P., and Tullis D.E. Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood. Chest 126 (2004) 1215-1224
-
(2004)
Chest
, vol.126
, pp. 1215-1224
-
-
Gilljam, M.1
Ellis, L.2
Corey, M.3
Zielenski, J.4
Durie, P.5
Tullis, D.E.6
-
9
-
-
0028806462
-
Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years
-
Gan K.H., Geus W.P., Bakker W., Lamers C.B., and Heijerman H.G. Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years. Thorax 50 (1995) 1301-1304
-
(1995)
Thorax
, vol.50
, pp. 1301-1304
-
-
Gan, K.H.1
Geus, W.P.2
Bakker, W.3
Lamers, C.B.4
Heijerman, H.G.5
-
10
-
-
0021987550
-
Newly diagnosed cystic fibrosis in middle and later life
-
Hunt B., and Geddes D.M. Newly diagnosed cystic fibrosis in middle and later life. Thorax 40 (1985) 23-26
-
(1985)
Thorax
, vol.40
, pp. 23-26
-
-
Hunt, B.1
Geddes, D.M.2
-
11
-
-
0018837203
-
Prolonged survival in an adult with cystic fibrosis
-
Sanders J.S., Pryor T.D., and Wedel M.K. Prolonged survival in an adult with cystic fibrosis. Chest 77 (1980) 226-227
-
(1980)
Chest
, vol.77
, pp. 226-227
-
-
Sanders, J.S.1
Pryor, T.D.2
Wedel, M.K.3
-
12
-
-
20144385873
-
Late diagnosis defines a unique population of long-term survivors of cystic fibrosis
-
Rodman D.M., Polis J.M., Heltshe S.L., et al. Late diagnosis defines a unique population of long-term survivors of cystic fibrosis. Am J Respir Crit Care Med 171 (2005) 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
-
14
-
-
0027402790
-
Standardised lung function testing
-
Gibson G.J. Standardised lung function testing. Eur Respir J 6 (1993) 155-157
-
(1993)
Eur Respir J
, vol.6
, pp. 155-157
-
-
Gibson, G.J.1
-
15
-
-
0026316543
-
Cystic fibrosis: current survival and population estimates to the year 2000
-
Elborn J.S., Shale D.J., and Britton J.R. Cystic fibrosis: current survival and population estimates to the year 2000. Thorax 46 (1991) 881-885
-
(1991)
Thorax
, vol.46
, pp. 881-885
-
-
Elborn, J.S.1
Shale, D.J.2
Britton, J.R.3
-
16
-
-
0027517995
-
Correlation between genotype and phenotype in patients with cystic fibrosis. The cystic fibrosis genotype-phenotype consortium
-
Correlation between genotype and phenotype in patients with cystic fibrosis. The cystic fibrosis genotype-phenotype consortium. N Engl J Med 329 (1993) 1308-1313
-
(1993)
N Engl J Med
, vol.329
, pp. 1308-1313
-
-
-
17
-
-
0036320272
-
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis
-
Emerson J., Rosenfeld M., McNamara S., Ramsey B., and Gibson R.L. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 34 (2002) 91-100
-
(2002)
Pediatr Pulmonol
, vol.34
, pp. 91-100
-
-
Emerson, J.1
Rosenfeld, M.2
McNamara, S.3
Ramsey, B.4
Gibson, R.L.5
-
18
-
-
0032797445
-
Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype
-
Parad R.B., Gerard C.J., Zurakowski D., Nichols D.P., and Pier G.B. Pulmonary outcome in cystic fibrosis is influenced primarily by mucoid Pseudomonas aeruginosa infection and immune status and only modestly by genotype. Infect Immun 67 (1999) 4744-4750
-
(1999)
Infect Immun
, vol.67
, pp. 4744-4750
-
-
Parad, R.B.1
Gerard, C.J.2
Zurakowski, D.3
Nichols, D.P.4
Pier, G.B.5
-
19
-
-
0029120290
-
The age at onset of chronic Pseudomonas aeruginosa colonization in cystic fibrosis - prognostic significance
-
Aebi C., Bracher R., Liechti-Gallati S., Tschappeler H., Rudeberg A., and Kraemer R. The age at onset of chronic Pseudomonas aeruginosa colonization in cystic fibrosis - prognostic significance. Eur J Pediatr 154 (1995) S69-S73
-
(1995)
Eur J Pediatr
, vol.154
-
-
Aebi, C.1
Bracher, R.2
Liechti-Gallati, S.3
Tschappeler, H.4
Rudeberg, A.5
Kraemer, R.6
-
20
-
-
0029016495
-
Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection
-
Demko C.A., Byard P.J., and Davis P.B. Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection. J Clin Epidemiol 48 (1995) 1041-1049
-
(1995)
J Clin Epidemiol
, vol.48
, pp. 1041-1049
-
-
Demko, C.A.1
Byard, P.J.2
Davis, P.B.3
-
22
-
-
0035129011
-
Methicillin resistant Staphylococcus aureus (MRSA) infection in cystic fibrosis
-
Miall L.S., McGinley N.T., Brownlee K.G., and Conway S.P. Methicillin resistant Staphylococcus aureus (MRSA) infection in cystic fibrosis. Arch Dis Child 84 (2001) 160-162
-
(2001)
Arch Dis Child
, vol.84
, pp. 160-162
-
-
Miall, L.S.1
McGinley, N.T.2
Brownlee, K.G.3
Conway, S.P.4
-
23
-
-
0031756804
-
Methicillin-resistant Staphylococcus aureus: impact at a national cystic fibrosis centre
-
Thomas S.R., Gyi K.M., Gaya H., and Hodson M.E. Methicillin-resistant Staphylococcus aureus: impact at a national cystic fibrosis centre. J Hosp Infect 40 (1998) 203-209
-
(1998)
J Hosp Infect
, vol.40
, pp. 203-209
-
-
Thomas, S.R.1
Gyi, K.M.2
Gaya, H.3
Hodson, M.E.4
-
24
-
-
14844303461
-
Prospective evaluation of emerging bacteria in cystic fibrosis
-
Steinkamp G., Wiedemann B., Rietschel E., et al. Prospective evaluation of emerging bacteria in cystic fibrosis. J Cyst Fibros 4 (2005) 41-48
-
(2005)
J Cyst Fibros
, vol.4
, pp. 41-48
-
-
Steinkamp, G.1
Wiedemann, B.2
Rietschel, E.3
-
25
-
-
0031903084
-
Abnormal glucose metabolism in cystic fibrosis
-
Moran A., Doherty L., Wang X., and Thomas W. Abnormal glucose metabolism in cystic fibrosis. J Pediatr 133 (1998) 10-17
-
(1998)
J Pediatr
, vol.133
, pp. 10-17
-
-
Moran, A.1
Doherty, L.2
Wang, X.3
Thomas, W.4
-
26
-
-
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 45 (1999) 61-73
-
(1999)
Diabetes Res Clin Pract
, vol.45
, pp. 61-73
-
-
Moran, A.1
Hardin, D.2
Rodman, D.3
-
27
-
-
0028978492
-
Glucose tolerance in patients with cystic fibrosis: five year prospective study
-
Lanng S., Hansen A., Thorsteinsson B., Nerup J., and Koch C. Glucose tolerance in patients with cystic fibrosis: five year prospective study. BMJ 311 (1995) 655-659
-
(1995)
BMJ
, vol.311
, pp. 655-659
-
-
Lanng, S.1
Hansen, A.2
Thorsteinsson, B.3
Nerup, J.4
Koch, C.5
-
28
-
-
0023866543
-
Diabetes mellitus associated with cystic fibrosis
-
Finkelstein S.M., Wielinski C.L., Elliott G.R., et al. Diabetes mellitus associated with cystic fibrosis. J Pediatr 112 (1988) 373-377
-
(1988)
J Pediatr
, vol.112
, pp. 373-377
-
-
Finkelstein, S.M.1
Wielinski, C.L.2
Elliott, G.R.3
-
29
-
-
24144434990
-
Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis
-
Milla C.E., Billings J., and Moran A. Diabetes is associated with dramatically decreased survival in female but not male subjects with cystic fibrosis. Diabetes Care 28 (2005) 2141-2144
-
(2005)
Diabetes Care
, vol.28
, pp. 2141-2144
-
-
Milla, C.E.1
Billings, J.2
Moran, A.3
-
30
-
-
23744470766
-
Pneumothorax in cystic fibrosis
-
Flume P.A., Strange C., Ye X., Ebeling M., Hulsey T., and Clark L.L. Pneumothorax in cystic fibrosis. Chest 128 (2005) 720-728
-
(2005)
Chest
, vol.128
, pp. 720-728
-
-
Flume, P.A.1
Strange, C.2
Ye, X.3
Ebeling, M.4
Hulsey, T.5
Clark, L.L.6
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