-
1
-
-
59349096268
-
-
Cystic Fibrosis Foundation. Cystic Fibrosis Foundation Patient Registry, 2006 Annual Data Report. Bethesda, Maryland, 2006.
-
Cystic Fibrosis Foundation. Cystic Fibrosis Foundation Patient Registry, 2006 Annual Data Report. Bethesda, Maryland, 2006.
-
-
-
-
2
-
-
0141615605
-
The phenotypic consequences of CFTR mutations
-
Rowntree R.K., and Harris A. The phenotypic consequences of CFTR mutations. Ann Hum Genet 67 (2003) 471-485
-
(2003)
Ann Hum Genet
, vol.67
, pp. 471-485
-
-
Rowntree, R.K.1
Harris, A.2
-
4
-
-
0033724681
-
Lung disease associated with the IVS8 5T allele of the CFTR gene
-
Noone P.G., Pue C.A., Zhou Z., et al. Lung disease associated with the IVS8 5T allele of the CFTR gene. Am J Respir Crit Care Med 162 (2000) 1919-1924
-
(2000)
Am J Respir Crit Care Med
, vol.162
, pp. 1919-1924
-
-
Noone, P.G.1
Pue, C.A.2
Zhou, Z.3
-
5
-
-
1642493936
-
Airway inflammation and infection in congenital bilateral absence of the vas deferens
-
Epub 2003 Oct 9
-
Gilljam M., Moltyaner Y., Downey G.P., et al. Airway inflammation and infection in congenital bilateral absence of the vas deferens. Am J Respir Crit Care Med 169 (2004) 174-179 Epub 2003 Oct 9
-
(2004)
Am J Respir Crit Care Med
, vol.169
, pp. 174-179
-
-
Gilljam, M.1
Moltyaner, Y.2
Downey, G.P.3
-
6
-
-
0027517995
-
-
Correlation between genotype and phenotype in patients with cystic fibrosis. The Cystic Fibrosis Genotype-Phenotype Consortium. N Engl J Med 1993;329:1308-1313.
-
Correlation between genotype and phenotype in patients with cystic fibrosis. The Cystic Fibrosis Genotype-Phenotype Consortium. N Engl J Med 1993;329:1308-1313.
-
-
-
-
7
-
-
33751242495
-
CFTR genotype as a predictor of prognosis in cystic fibrosis
-
McKone E.F., Goss C.H., and Aitken M.L. CFTR genotype as a predictor of prognosis in cystic fibrosis. Chest 130 (2006) 1441-1447
-
(2006)
Chest
, vol.130
, pp. 1441-1447
-
-
McKone, E.F.1
Goss, C.H.2
Aitken, M.L.3
-
8
-
-
33749328098
-
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis
-
Epub 2006 Jul 24
-
Blackman S.M., Deering-Brose R., et al. Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis. Gastroenterology 131 (2006) 1030-1039 Epub 2006 Jul 24
-
(2006)
Gastroenterology
, vol.131
, pp. 1030-1039
-
-
Blackman, S.M.1
Deering-Brose, R.2
-
10
-
-
0037157787
-
Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes
-
Salvatore F., Scudiero O., and Castaldo G. Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes. Am J Med Genet 111 (2002) 88-95
-
(2002)
Am J Med Genet
, vol.111
, pp. 88-95
-
-
Salvatore, F.1
Scudiero, O.2
Castaldo, G.3
-
11
-
-
25844491194
-
Genetic modifiers of lung disease in cystic fibrosis
-
for the Gene Modifier Study Group
-
Drumm M.L., Konstan M.W., Schluchter M.D., et al., for the Gene Modifier Study Group. Genetic modifiers of lung disease in cystic fibrosis. N Engl J Med 3531 (2005) 1443-1453
-
(2005)
N Engl J Med
, vol.3531
, pp. 1443-1453
-
-
Drumm, M.L.1
Konstan, M.W.2
Schluchter, M.D.3
-
12
-
-
0347812948
-
Genetics of cystic fibrosis
-
Gallati S. Genetics of cystic fibrosis. Semin Respir Crit Care Med 24 (2003) 629-638
-
(2003)
Semin Respir Crit Care Med
, vol.24
, pp. 629-638
-
-
Gallati, S.1
-
13
-
-
0037208909
-
Genes in the vicinity of CFTR modulate the cystic fibrosis phenotype in highly concordant or discordant F508del homozygous sib pairs
-
Mekus F., Laabs U., Veeze H., and Tümmler B. Genes in the vicinity of CFTR modulate the cystic fibrosis phenotype in highly concordant or discordant F508del homozygous sib pairs. Hum Genet 112 (2003) 1-11
-
(2003)
Hum Genet
, vol.112
, pp. 1-11
-
-
Mekus, F.1
Laabs, U.2
Veeze, H.3
Tümmler, B.4
-
14
-
-
33747285792
-
Modifier effect of the Toll-like receptor 4 D299G polymorphism in children with cystic fibrosis
-
Urquhart D.S., Allen J., Elrayess M., Fidler K., Klein N., and Jaffe A. Modifier effect of the Toll-like receptor 4 D299G polymorphism in children with cystic fibrosis. Archivum Immunologiae et Therapiae Experimentalis 54 (2006) 271-276
-
(2006)
Archivum Immunologiae et Therapiae Experimentalis
, vol.54
, pp. 271-276
-
-
Urquhart, D.S.1
Allen, J.2
Elrayess, M.3
Fidler, K.4
Klein, N.5
Jaffe, A.6
-
15
-
-
0036163928
-
Case-mix adjustment for evaluation of mortality in cystic fibrosis
-
for the Northern New England Cystic Fibrosis Consortium
-
O'Connor G.T., Quinton H.B., Kahn R., et al., for the Northern New England Cystic Fibrosis Consortium. Case-mix adjustment for evaluation of mortality in cystic fibrosis. Pediatr Pulmonol 33 (2002) 99-105
-
(2002)
Pediatr Pulmonol
, vol.33
, pp. 99-105
-
-
O'Connor, G.T.1
Quinton, H.B.2
Kahn, R.3
-
16
-
-
0030967472
-
Gender gap in cystic fibrosis mortality
-
Rosenfeld M., Davis R., FitzSimmons S., Pepe M., and Ramsey B. Gender gap in cystic fibrosis mortality. Am J Epidemiol 145 (1997) 794-803
-
(1997)
Am J Epidemiol
, vol.145
, pp. 794-803
-
-
Rosenfeld, M.1
Davis, R.2
FitzSimmons, S.3
Pepe, M.4
Ramsey, B.5
-
17
-
-
27144501047
-
Is there still a gender gap in cystic fibrosis?
-
Verma N., Bush A., and Buchdahl R. Is there still a gender gap in cystic fibrosis?. Chest 128 (2005) 2824-2834
-
(2005)
Chest
, vol.128
, pp. 2824-2834
-
-
Verma, N.1
Bush, A.2
Buchdahl, R.3
-
18
-
-
12244306198
-
Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening
-
Maselli J.H., Sontag M.K., Norris J.M., MacKenzie T., Wagener J.S., and Accurso F.J. Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening. Pediatr Pulmonol 35 (2003) 257-262
-
(2003)
Pediatr Pulmonol
, vol.35
, pp. 257-262
-
-
Maselli, J.H.1
Sontag, M.K.2
Norris, J.M.3
MacKenzie, T.4
Wagener, J.S.5
Accurso, F.J.6
-
19
-
-
0037238549
-
Differences in resting energy expenditure between male and female children with cystic fibrosis
-
Allen J.R., McCauley J.C., Selby A.M., et al. Differences in resting energy expenditure between male and female children with cystic fibrosis. J Pediatr 142 (2003) 15-19
-
(2003)
J Pediatr
, vol.142
, pp. 15-19
-
-
Allen, J.R.1
McCauley, J.C.2
Selby, A.M.3
-
20
-
-
0034873470
-
Gendered embodiment and survival for young people with cystic fibrosis
-
Willis E., Miller R., and Wyn J. Gendered embodiment and survival for young people with cystic fibrosis. Soc Sci Med 53 (2001) 1163-1174
-
(2001)
Soc Sci Med
, vol.53
, pp. 1163-1174
-
-
Willis, E.1
Miller, R.2
Wyn, J.3
-
21
-
-
17544389292
-
Body image and dieting behavior in cystic fibrosis
-
Truby H., and Paxton A.S. Body image and dieting behavior in cystic fibrosis. Pediatrics 107 (2001) e92
-
(2001)
Pediatrics
, vol.107
-
-
Truby, H.1
Paxton, A.S.2
-
22
-
-
0027178197
-
Socioeconomic inequalities in health. No easy solution
-
Adler N.E., Boyce W.T., Chesney M.A., Folkman S., and Syme S.L. Socioeconomic inequalities in health. No easy solution. JAMA 269 (1993) 3140-3145
-
(1993)
JAMA
, vol.269
, pp. 3140-3145
-
-
Adler, N.E.1
Boyce, W.T.2
Chesney, M.A.3
Folkman, S.4
Syme, S.L.5
-
23
-
-
0024590336
-
Effects of social class, sex, and region of residence on age at death from cystic fibrosis
-
Britton J.R. Effects of social class, sex, and region of residence on age at death from cystic fibrosis. BMJ 298 (1989) 483-487
-
(1989)
BMJ
, vol.298
, pp. 483-487
-
-
Britton, J.R.1
-
24
-
-
0034987271
-
The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States
-
Schechter M.S., Shelton B.J., Margolis P.A., and Fitzsimmons S.C. The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States. Am J Respir Crit Care Med 163 (2001) 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
Fitzsimmons, S.C.4
-
25
-
-
0037390820
-
Median household income and mortality rate in cystic fibrosis
-
O'Connor G.T., Quinton H.B., Kneeland T., et al. Median household income and mortality rate in cystic fibrosis. Pediatrics 111 (2003) e333-e339
-
(2003)
Pediatrics
, vol.111
-
-
O'Connor, G.T.1
Quinton, H.B.2
Kneeland, T.3
-
26
-
-
0026556587
-
Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion
-
Campbell III P.W., Parker R.A., Roberts B.T., Krishnamani M.R., and Phillips III J.A. Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion. J Pediatr 120 (1992) 261-264
-
(1992)
J Pediatr
, vol.120
, pp. 261-264
-
-
Campbell III, P.W.1
Parker, R.A.2
Roberts, B.T.3
Krishnamani, M.R.4
Phillips III, J.A.5
-
27
-
-
0025007903
-
Exposure of children with cystic fibrosis to environmental tobacco smoke
-
Rubin B.K. Exposure of children with cystic fibrosis to environmental tobacco smoke. N Engl J Med 323 (1990) 782-788
-
(1990)
N Engl J Med
, vol.323
, pp. 782-788
-
-
Rubin, B.K.1
-
28
-
-
0027331557
-
Passive smoking and lung function in cystic fibrosis
-
Kovesi T., Corey M., and Levison H. Passive smoking and lung function in cystic fibrosis. Am Rev Respir Dis 148 (1993) 1266-1271
-
(1993)
Am Rev Respir Dis
, vol.148
, pp. 1266-1271
-
-
Kovesi, T.1
Corey, M.2
Levison, H.3
-
29
-
-
0031887257
-
The impact of individual and area characteristics on urban socioeconomic differences in health and smoking
-
Reijneveld S.A. The impact of individual and area characteristics on urban socioeconomic differences in health and smoking. Int J Epidemiol 27 (1998) 33-40
-
(1998)
Int J Epidemiol
, vol.27
, pp. 33-40
-
-
Reijneveld, S.A.1
-
30
-
-
4444367099
-
The effect of air pollution on lung development from 10 to 18 years of age
-
Gauderman W.J., Avol E., Gilliland F., et al. The effect of air pollution on lung development from 10 to 18 years of age. N Engl J Med 351 (2004) 1057-1067
-
(2004)
N Engl J Med
, vol.351
, pp. 1057-1067
-
-
Gauderman, W.J.1
Avol, E.2
Gilliland, F.3
-
31
-
-
0028911083
-
Particulate air pollution as a predictor of mortality in a prospective study of U
-
Pope III C.A., Thun M.J., Namboodiri M.M., et al. Particulate air pollution as a predictor of mortality in a prospective study of U. S. adults. Am J Respir Crit Care Med 151 (1995) 669-674
-
(1995)
S. adults. Am J Respir Crit Care Med
, vol.151
, pp. 669-674
-
-
Pope III, C.A.1
Thun, M.J.2
Namboodiri, M.M.3
-
32
-
-
27344454718
-
Environmental equity, air quality, socioeconomic status, and respiratory health: a linkage analysis of routine data from the Health Survey for England
-
Wheeler B.W., and Ben-Shlomo Y. Environmental equity, air quality, socioeconomic status, and respiratory health: a linkage analysis of routine data from the Health Survey for England. J Epidemiol Community Health 59 (2005) 948-954
-
(2005)
J Epidemiol Community Health
, vol.59
, pp. 948-954
-
-
Wheeler, B.W.1
Ben-Shlomo, Y.2
-
33
-
-
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
-
34
-
-
0035002870
-
Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis
-
Nixon G.M., Armstrong D.S., Carzino R., et al. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J Pediatr 138 (2001) 699-704
-
(2001)
J Pediatr
, vol.138
, pp. 699-704
-
-
Nixon, G.M.1
Armstrong, D.S.2
Carzino, R.3
-
35
-
-
0034785481
-
Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition
-
Kosorok M.R., Zeng L., West S.E., et al. Acceleration of lung disease in children with cystic fibrosis after Pseudomonas aeruginosa acquisition. Pediatr Pulmonol 32 (2001) 277-287
-
(2001)
Pediatr Pulmonol
, vol.32
, pp. 277-287
-
-
Kosorok, M.R.1
Zeng, L.2
West, S.E.3
-
36
-
-
34447530328
-
Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis
-
for the Scientific Advisory Group, the Investigators, Coordinators of the Epidemiologic Study of Cystic Fibrosis 139.e1. Epub 2007 Jun 22
-
Konstan M.W., Morgan W.J., Butler S.M., et al., for the Scientific Advisory Group, the Investigators, Coordinators of the Epidemiologic Study of Cystic Fibrosis. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis. J Pediatr 151 (2007) 134-139 139.e1. Epub 2007 Jun 22
-
(2007)
J Pediatr
, vol.151
, pp. 134-139
-
-
Konstan, M.W.1
Morgan, W.J.2
Butler, S.M.3
-
37
-
-
0036220978
-
Antibiotic prophylaxis in infants and young children with cystic fibrosis: a randomized controlled trial
-
Stutman H.R., Lieberman J.M., Nussbaum E., and Marks M.I. Antibiotic prophylaxis in infants and young children with cystic fibrosis: a randomized controlled trial. J Pediatr 140 (2002) 299-305
-
(2002)
J Pediatr
, vol.140
, pp. 299-305
-
-
Stutman, H.R.1
Lieberman, J.M.2
Nussbaum, E.3
Marks, M.I.4
-
38
-
-
0035125425
-
Effect of continuous antistaphylococcal therapy on the rate of P. aeruginosa acquisition in patients with cystic fibrosis
-
for the German Board of the European Registry for Cystic Fibrosis (ERCF)
-
Ratjen F., Comes G., Paul K., Posselt H.G., Wagner T.O., Harms K., and for the German Board of the European Registry for Cystic Fibrosis (ERCF). Effect of continuous antistaphylococcal therapy on the rate of P. aeruginosa acquisition in patients with cystic fibrosis. Pediatr Pulmonol 31 (2001) 13-16
-
(2001)
Pediatr Pulmonol
, vol.31
, pp. 13-16
-
-
Ratjen, F.1
Comes, G.2
Paul, K.3
Posselt, H.G.4
Wagner, T.O.5
Harms, K.6
-
39
-
-
0036846398
-
Increased treatment requirements of patients with cystic fibrosis who harbour a highly transmissible strain of Pseudomonas aeruginosa
-
Jones A.M., Dodd M.E., Doherty C.J., Govan J.R., and Webb A.K. Increased treatment requirements of patients with cystic fibrosis who harbour a highly transmissible strain of Pseudomonas aeruginosa. Thorax 57 (2002) 924-925
-
(2002)
Thorax
, vol.57
, pp. 924-925
-
-
Jones, A.M.1
Dodd, M.E.2
Doherty, C.J.3
Govan, J.R.4
Webb, A.K.5
-
40
-
-
0026000699
-
Nosocomial acquisition of Pseudomonas aeruginosa by cystic fibrosis patients
-
Tümmler B., Koopmann U., Grothues D., Weissbrodt H., Steinkamp G., and von der Hardt H. Nosocomial acquisition of Pseudomonas aeruginosa by cystic fibrosis patients. J Clin Microbiol 29 (1991) 1265-1267
-
(1991)
J Clin Microbiol
, vol.29
, pp. 1265-1267
-
-
Tümmler, B.1
Koopmann, U.2
Grothues, D.3
Weissbrodt, H.4
Steinkamp, G.5
von der Hardt, H.6
-
41
-
-
0031873820
-
Comprehensive analysis of risk factors for acquisition of Pseudomonas aeruginosa in young children with cystic fibrosis
-
Kosorok M.R., Jalaluddin M., Farrell P.M., et al. Comprehensive analysis of risk factors for acquisition of Pseudomonas aeruginosa in young children with cystic fibrosis. Pediatr Pulmonol 26 (1998) 81-88
-
(1998)
Pediatr Pulmonol
, vol.26
, pp. 81-88
-
-
Kosorok, M.R.1
Jalaluddin, M.2
Farrell, P.M.3
-
42
-
-
0024605489
-
Estimated risk of cross-infection with Pseudomonas aeruginosa in Danish cystic fibrosis patients
-
Høiby N., and Pedersen S.S. Estimated risk of cross-infection with Pseudomonas aeruginosa in Danish cystic fibrosis patients. Acta Paediatr Scand 78 (1989) 395-404
-
(1989)
Acta Paediatr Scand
, vol.78
, pp. 395-404
-
-
Høiby, N.1
Pedersen, S.S.2
-
43
-
-
0022504440
-
Does centralized treatment of cystic fibrosis increase the risk of Pseudomonas aeruginosa infection?
-
Pedersen S.S., Jensen T., Pressler T., Høiby N., and Rosendal K. Does centralized treatment of cystic fibrosis increase the risk of Pseudomonas aeruginosa infection?. Acta Paediatr Scand 75 (1986) 840-845
-
(1986)
Acta Paediatr Scand
, vol.75
, pp. 840-845
-
-
Pedersen, S.S.1
Jensen, T.2
Pressler, T.3
Høiby, N.4
Rosendal, K.5
-
44
-
-
0025313244
-
Risk factors for Pseudomonas aeruginosa colonization in cystic fibrosis patients
-
Kerem E., Corey M., Stein R., Gold R., and Levison H. Risk factors for Pseudomonas aeruginosa colonization in cystic fibrosis patients. Pediatr Infect Dis J 9 (1990) 494-498
-
(1990)
Pediatr Infect Dis J
, vol.9
, pp. 494-498
-
-
Kerem, E.1
Corey, M.2
Stein, R.3
Gold, R.4
Levison, H.5
-
45
-
-
0032424454
-
Severe viral respiratory infections in infants with cystic fibrosis
-
Armstrong D., Grimwood K., Carlin J.B., et al. Severe viral respiratory infections in infants with cystic fibrosis. Pediatr Pulmonol 26 (1998) 371-379
-
(1998)
Pediatr Pulmonol
, vol.26
, pp. 371-379
-
-
Armstrong, D.1
Grimwood, K.2
Carlin, J.B.3
-
46
-
-
0035503325
-
Infection with Burkholderia cepacia complex genomovars in patients with cystic fibrosis: virulent transmissible strains of genomovar III can replace Burkholderia multivorans
-
Epub 2001 Oct 4
-
Mahenthiralingam E., Vandamme P., Campbell M.E., et al. Infection with Burkholderia cepacia complex genomovars in patients with cystic fibrosis: virulent transmissible strains of genomovar III can replace Burkholderia multivorans. Clin Infect Dis 33 (2001) 1469-1475 Epub 2001 Oct 4
-
(2001)
Clin Infect Dis
, vol.33
, pp. 1469-1475
-
-
Mahenthiralingam, E.1
Vandamme, P.2
Campbell, M.E.3
-
47
-
-
0035944832
-
Burkholderia cepacia complex genomovars and pulmonary transplantation outcomes in patients with cystic fibrosis
-
De Soyza A., McDowell A., Archer L., et al. Burkholderia cepacia complex genomovars and pulmonary transplantation outcomes in patients with cystic fibrosis. Lancet 358 (2001) 1780-1781
-
(2001)
Lancet
, vol.358
, pp. 1780-1781
-
-
De Soyza, A.1
McDowell, A.2
Archer, L.3
-
48
-
-
0035659459
-
Lung transplantation for cystic fibrosis patients with Burkholderia cepacia complex. Survival linked to genomovar type
-
Aris R.M., Routh J.C., LiPuma J.J., Heath D.G., and Gilligan P.H. Lung transplantation for cystic fibrosis patients with Burkholderia cepacia complex. Survival linked to genomovar type. Am J Respir Crit Care Med 164 (2001) 2102-2106
-
(2001)
Am J Respir Crit Care Med
, vol.164
, pp. 2102-2106
-
-
Aris, R.M.1
Routh, J.C.2
LiPuma, J.J.3
Heath, D.G.4
Gilligan, P.H.5
-
49
-
-
34848890028
-
Update on the epidemiology and management of Staphylococcus aureus, including methicillin-resistant Staphylococcus aureus, in patients with cystic fibrosis
-
Stone A., and Saiman L. Update on the epidemiology and management of Staphylococcus aureus, including methicillin-resistant Staphylococcus aureus, in patients with cystic fibrosis. Curr Opin Pulm Med 13 (2007) 515-521
-
(2007)
Curr Opin Pulm Med
, vol.13
, pp. 515-521
-
-
Stone, A.1
Saiman, L.2
-
50
-
-
34249880451
-
Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function
-
for the Investigators, Coordinators of the Epidemiologic Study of Cystic Fibrosis
-
Ren C.L., Morgan W.J., Konstan M.W., et al., for the Investigators, Coordinators of the Epidemiologic Study of Cystic Fibrosis. Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function. Pediatr Pulmonol 42 (2007) 513-518
-
(2007)
Pediatr Pulmonol
, vol.42
, pp. 513-518
-
-
Ren, C.L.1
Morgan, W.J.2
Konstan, M.W.3
-
51
-
-
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
-
52
-
-
0029027898
-
Effect of respiratory virus infections including rhinovirus on clinical status in cystic fibrosis
-
Smyth A.R., Smyth R.L., Tong C.Y., Hart C.A., and Heaf D.P. Effect of respiratory virus infections including rhinovirus on clinical status in cystic fibrosis. Arch Dis Child 73 (1995) 117-120
-
(1995)
Arch Dis Child
, vol.73
, pp. 117-120
-
-
Smyth, A.R.1
Smyth, R.L.2
Tong, C.Y.3
Hart, C.A.4
Heaf, D.P.5
-
53
-
-
0029805758
-
Effects of upper respiratory tract infections in patients with cystic fibrosis
-
Collinson J., Nicholson K.G., Cancio E., et al. Effects of upper respiratory tract infections in patients with cystic fibrosis. Thorax 51 (1996) 1115-1122
-
(1996)
Thorax
, vol.51
, pp. 1115-1122
-
-
Collinson, J.1
Nicholson, K.G.2
Cancio, E.3
-
54
-
-
0021687443
-
Association of respiratory viral infections with pulmonary deterioration in patients with cystic fibrosis
-
Wang E.E., Prober C.G., Manson B., Corey M., and Levison H. Association of respiratory viral infections with pulmonary deterioration in patients with cystic fibrosis. N Engl J Med 311 (1984) 1653-1658
-
(1984)
N Engl J Med
, vol.311
, pp. 1653-1658
-
-
Wang, E.E.1
Prober, C.G.2
Manson, B.3
Corey, M.4
Levison, H.5
-
55
-
-
0033064891
-
Effects of viral lower respiratory tract infection on lung function in infants with cystic fibrosis
-
Hiatt P.W., Grace S.C., Kozinetz C.A., et al. Effects of viral lower respiratory tract infection on lung function in infants with cystic fibrosis. Pediatrics 103 (1999) 619-626
-
(1999)
Pediatrics
, vol.103
, pp. 619-626
-
-
Hiatt, P.W.1
Grace, S.C.2
Kozinetz, C.A.3
-
56
-
-
0030022826
-
Compliance with treatment in adult patients with cystic fibrosis
-
Conway S.P., Pond M.N., Hamnett T., and Watson A. Compliance with treatment in adult patients with cystic fibrosis. Thorax 51 (1996) 29-33
-
(1996)
Thorax
, vol.51
, pp. 29-33
-
-
Conway, S.P.1
Pond, M.N.2
Hamnett, T.3
Watson, A.4
-
57
-
-
0002952740
-
Measuring adherence to medical treatments in childhood chronic illness: considering multiple methods and sources of information
-
Quittner A.L., Espelage D.L., Ievers-Landis C., and Drotar D. Measuring adherence to medical treatments in childhood chronic illness: considering multiple methods and sources of information. J Clin Psychol Med Settings 7 (2000) 41-54
-
(2000)
J Clin Psychol Med Settings
, vol.7
, pp. 41-54
-
-
Quittner, A.L.1
Espelage, D.L.2
Ievers-Landis, C.3
Drotar, D.4
-
58
-
-
0029802115
-
Health perceptions and treatment adherence in adults with cystic fibrosis
-
Abbott J., Dodd M., and Webb A.K. Health perceptions and treatment adherence in adults with cystic fibrosis. Thorax 51 (1996) 1233-1238
-
(1996)
Thorax
, vol.51
, pp. 1233-1238
-
-
Abbott, J.1
Dodd, M.2
Webb, A.K.3
-
59
-
-
0021241325
-
Overview of patient compliance with medication dosing: a literature review
-
Greenberg R.N. Overview of patient compliance with medication dosing: a literature review. Clin Ther 6 (1984) 592-599
-
(1984)
Clin Ther
, vol.6
, pp. 592-599
-
-
Greenberg, R.N.1
-
61
-
-
0026210624
-
Perceptions of medical compliance in children and adolescents with cystic fibrosis
-
Gudas L.J., Koocher G.P., and Wypij D. Perceptions of medical compliance in children and adolescents with cystic fibrosis. J Dev Behav Pediatr 12 (1991) 236-242
-
(1991)
J Dev Behav Pediatr
, vol.12
, pp. 236-242
-
-
Gudas, L.J.1
Koocher, G.P.2
Wypij, D.3
-
62
-
-
0027518559
-
Family correlates of a 10-year pulmonary health trend in cystic fibrosis
-
Patterson J.M., Budd J., Goetz D., and Warwick W.J. Family correlates of a 10-year pulmonary health trend in cystic fibrosis. Pediatrics 91 (1993) 383-389
-
(1993)
Pediatrics
, vol.91
, pp. 383-389
-
-
Patterson, J.M.1
Budd, J.2
Goetz, D.3
Warwick, W.J.4
-
63
-
-
0025132149
-
The impact of family functioning on health changes in children with cystic fibrosis
-
Patterson J.M., McCubbin H.I., and Warwick W.J. The impact of family functioning on health changes in children with cystic fibrosis. Soc Sci Med 31 (1990) 159-164
-
(1990)
Soc Sci Med
, vol.31
, pp. 159-164
-
-
Patterson, J.M.1
McCubbin, H.I.2
Warwick, W.J.3
-
64
-
-
0028008502
-
Enhancing patient adherence to medical recommendations
-
DiMatteo M.R. Enhancing patient adherence to medical recommendations. JAMA 271 (1994) 79-82
-
(1994)
JAMA
, vol.271
, pp. 79-82
-
-
DiMatteo, M.R.1
-
65
-
-
0033209403
-
Knowledge of physician prescriptions and adherence to treatment among children with cystic fibrosis and their mothers
-
Ievers C.E., Brown R.T., Drotar D., Caplan D., Pishevar B.S., and Lambert R.G. Knowledge of physician prescriptions and adherence to treatment among children with cystic fibrosis and their mothers. J Dev Behav Pediatr 20 (1999) 335-343
-
(1999)
J Dev Behav Pediatr
, vol.20
, pp. 335-343
-
-
Ievers, C.E.1
Brown, R.T.2
Drotar, D.3
Caplan, D.4
Pishevar, B.S.5
Lambert, R.G.6
-
66
-
-
0028233887
-
Non-adherence to treatment in cystic fibrosis
-
Lask B. Non-adherence to treatment in cystic fibrosis. J R Soc Med 87 Suppl 21 (1994) 25-27
-
(1994)
J R Soc Med
, vol.87
, Issue.SUPPL. 21
, pp. 25-27
-
-
Lask, B.1
-
67
-
-
0002339580
-
Adherence to medical treatments in adolescents with cystic fibrosis: the development and evaluation of family-based interventions
-
Drotar D. (Ed), Erlbaum Associates, Mahwah, NJ
-
Quittner A.L., Drotar D., Ievers-Landis C., Seidner D., Slocum N., and Jacobsen J. Adherence to medical treatments in adolescents with cystic fibrosis: the development and evaluation of family-based interventions. In: Drotar D. (Ed). Promoting Adherence to Medical Treatment in Childhood Chronic Illness: Concepts, Methods, and Interventions (2000), Erlbaum Associates, Mahwah, NJ
-
(2000)
Promoting Adherence to Medical Treatment in Childhood Chronic Illness: Concepts, Methods, and Interventions
-
-
Quittner, A.L.1
Drotar, D.2
Ievers-Landis, C.3
Seidner, D.4
Slocum, N.5
Jacobsen, J.6
-
68
-
-
0033391698
-
Psychosocial predictors of adherence to nutritional recommendations and growth outcomes in children with cystic fibrosis
-
Anthony H., Paxton S., Bines J., and Phelan P. Psychosocial predictors of adherence to nutritional recommendations and growth outcomes in children with cystic fibrosis. J Psychosom Res 47 (1999) 623-634
-
(1999)
J Psychosom Res
, vol.47
, pp. 623-634
-
-
Anthony, H.1
Paxton, S.2
Bines, J.3
Phelan, P.4
-
69
-
-
17744372496
-
Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group
-
Farrell P.M., Kosorok M.R., Rock M.J., et al. Early diagnosis of cystic fibrosis through neonatal screening prevents severe malnutrition and improves long-term growth. Wisconsin Cystic Fibrosis Neonatal Screening Study Group. Pediatrics 107 (2001) 1-13
-
(2001)
Pediatrics
, vol.107
, pp. 1-13
-
-
Farrell, P.M.1
Kosorok, M.R.2
Rock, M.J.3
-
70
-
-
33846910543
-
Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy
-
for the United Kingdom Cystic Fibrosis Database Steering Committee
-
Sims E.J., Clark A., McCormick J., Mehta G., Connett G., Mehta A., and for the United Kingdom Cystic Fibrosis Database Steering Committee. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy. Pediatrics 119 (2007) 19-28
-
(2007)
Pediatrics
, vol.119
, pp. 19-28
-
-
Sims, E.J.1
Clark, A.2
McCormick, J.3
Mehta, G.4
Connett, G.5
Mehta, A.6
-
71
-
-
34047269755
-
Economic implications of newborn screening for cystic fibrosis: a cost of illness retrospective cohort study
-
for the UK Cystic Fibrosis Database Steering Committee
-
Sims E.J., Mugford M., Clark A., et al., for the UK Cystic Fibrosis Database Steering Committee. Economic implications of newborn screening for cystic fibrosis: a cost of illness retrospective cohort study. Lancet 369 (2007) 1187-1195
-
(2007)
Lancet
, vol.369
, pp. 1187-1195
-
-
Sims, E.J.1
Mugford, M.2
Clark, A.3
-
72
-
-
25844453964
-
The influence of newborn screening for cystic fibrosis on pulmonary outcomes in New South Wales
-
McKay K.O., Waters D.L., and Gaskin K.J. The influence of newborn screening for cystic fibrosis on pulmonary outcomes in New South Wales. J Pediatr 147 Suppl 1 (2005) S47-S50
-
(2005)
J Pediatr
, vol.147
, Issue.SUPPL. 1
-
-
McKay, K.O.1
Waters, D.L.2
Gaskin, K.J.3
-
73
-
-
20144385873
-
Late diagnosis defines a unique population of long-term survivors of cystic fibrosis
-
Epub 2004 Dec 10
-
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 Epub 2004 Dec 10
-
(2005)
Am J Respir Crit Care Med.
, vol.171
, pp. 621-626
-
-
Rodman, D.M.1
Polis, J.M.2
Heltshe, S.L.3
-
74
-
-
0037100471
-
Delayed diagnosis of US females with cystic fibrosis
-
Lai H.C., Kosorok M.R., Laxova A., Makholm L.M., and Farrell P.M. Delayed diagnosis of US females with cystic fibrosis. Am J Epidemiol 156 (2002) 165-173
-
(2002)
Am J Epidemiol
, vol.156
, pp. 165-173
-
-
Lai, H.C.1
Kosorok, M.R.2
Laxova, A.3
Makholm, L.M.4
Farrell, P.M.5
-
75
-
-
35349017871
-
Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs
-
Farrell P., Joffe S., Foley L., Canny G.J., Mayne P., and Rosenberg M. Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs. Ir Med J 100 (2007) 557-560
-
(2007)
Ir Med J
, vol.100
, pp. 557-560
-
-
Farrell, P.1
Joffe, S.2
Foley, L.3
Canny, G.J.4
Mayne, P.5
Rosenberg, M.6
-
76
-
-
0034987271
-
The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States
-
Schechter M.S., Shelton B.J., Margolis P.A., and FitzSimmons S.C. The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States. Am J Respir Crit Care Med 163 (2001) 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
FitzSimmons, S.C.4
-
77
-
-
0032770883
-
Normal growth in cystic fibrosis associated with a specialised centre
-
Collins C.E., MacDonald-Wicks L., Rowe S., O'Loughlin E.V., and Henry R.L. Normal growth in cystic fibrosis associated with a specialised centre. Arch Dis Child 81 (1999) 241-246
-
(1999)
Arch Dis Child
, vol.81
, pp. 241-246
-
-
Collins, C.E.1
MacDonald-Wicks, L.2
Rowe, S.3
O'Loughlin, E.V.4
Henry, R.L.5
-
78
-
-
0032513942
-
Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study
-
Mahadeva R., Webb K., Westerbeek R.C., et al. Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study. BMJ 316 (1998) 1771-1775
-
(1998)
BMJ
, vol.316
, pp. 1771-1775
-
-
Mahadeva, R.1
Webb, K.2
Westerbeek, R.C.3
-
79
-
-
0037252230
-
Factors influencing outcomes in cystic fibrosis: a centre-based analysis
-
Johnson C., Butler S.M., Konstan M.W., Morgan W., and Wohl M.E. Factors influencing outcomes in cystic fibrosis: a centre-based analysis. Chest 123 (2003) 20-27
-
(2003)
Chest
, vol.123
, pp. 20-27
-
-
Johnson, C.1
Butler, S.M.2
Konstan, M.W.3
Morgan, W.4
Wohl, M.E.5
|