-
3
-
-
0033870680
-
Health status and sociodemographic characteristics of adults receiving a cystic fibrosis diagnosis after age 18 years
-
Widerman E, Millner L, Sexauer W, Fiel S. Health status and sociodemographic characteristics of adults receiving a cystic fibrosis diagnosis after age 18 years. Chest. 2000;118(2):427-433. (Pubitemid 30637811)
-
(2000)
Chest
, vol.118
, Issue.2
, pp. 427-433
-
-
Widerman, E.1
Millner, L.2
Sexauer, W.3
Fiel, S.4
-
4
-
-
6344231597
-
Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood
-
DOI 10.1378/chest.126.4.1215
-
Gilljam M, Ellis L, Corey M, Zielenski J, Durie P, Tullis DE. Clinical manifestations of cystic fibrosis among patients with diagnosis in adulthood. Chest. 2004;126(4):1215-1224. (Pubitemid 39391253)
-
(2004)
Chest
, vol.126
, Issue.4
, pp. 1215-1224
-
-
Gilljam, M.1
Ellis, L.2
Corey, M.3
Zielenski, J.4
Durie, P.5
Tullis, D.E.6
-
5
-
-
0033839380
-
Clinical features associated with a delayed diagnosis of cystic fibrosis
-
McCloskey M, Redmond AO, Hill A, Elborn JS. Clinical features associated with a delayed diagnosis of cystic fibrosis. Respiration. 2000;67(4):402-407. (Pubitemid 30666002)
-
(2000)
Respiration
, vol.67
, Issue.4
, pp. 402-407
-
-
McCloskey, M.1
Redmond, A.O.B.2
Hill, A.3
Elborn, J.S.4
-
6
-
-
0028806462
-
Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years
-
Gan KH, Geus WP, Bakker W, Lamers CB, Heijerman HG. Genetic and clinical features of patients with cystic fibrosis diagnosed after the age of 16 years. Thorax. 1995;50(12):1301-1304.
-
(1995)
Thorax
, vol.50
, Issue.12
, pp. 1301-1304
-
-
Gan, K.H.1
Geus, W.P.2
Bakker, W.3
Lamers, C.B.4
Heijerman, H.G.5
-
7
-
-
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(6):621-626.
-
(2005)
Am J Respir Crit Care Med
, vol.171
, Issue.6
, pp. 621-626
-
-
Rodman, D.M.1
Polis, J.M.2
Heltshe, S.L.3
-
8
-
-
0032926069
-
Spirometric reference values from a sample of the general U.S. population
-
Hankinson JL, Odencrantz JR, Fedan KB. Spirometric reference values from a sample of the general U.S. population. Am J Respir Crit Care Med. 1999;159(1):179-187.
-
(1999)
Am J Respir Crit Care Med
, vol.159
, Issue.1
, pp. 179-187
-
-
Hankinson, J.L.1
Odencrantz, J.R.2
Fedan, K.B.3
-
9
-
-
0033779665
-
Type I. Type I, II, III, IV, and V cystic fibrosis transmembrane conductance regulator defects and opportunities for therapy
-
Choo-Kang LR, Zeitlin PL, Type I. Type I, II, III, IV, and V cystic fibrosis transmembrane conductance regulator defects and opportunities for therapy. Curr Opin Pulm Med. 2000;6(6):521-529.
-
(2000)
Curr Opin Pulm Med
, vol.6
, Issue.6
, pp. 521-529
-
-
Choo-Kang, L.R.1
Zeitlin, P.L.2
-
11
-
-
0037445273
-
Nontuberculous mycobacteria. I: Multicenter prevalence study in cystic fibrosis
-
Nontuberculous Mycobacteria in Cystic Fibrosis Study Group
-
Olivier KN, Weber DJ, Wallace RJ Jr, et al; Nontuberculous Mycobacteria in Cystic Fibrosis Study Group. Nontuberculous mycobacteria. I: multicenter prevalence study in cystic fibrosis. Am J Respir Crit Care Med. 2003;167(6):828-834.
-
(2003)
Am J Respir Crit Care Med
, vol.167
, Issue.6
, pp. 828-834
-
-
Olivier, K.N.1
Weber, D.J.2
Wallace Jr., R.J.3
-
12
-
-
0026019534
-
Severity of cystic fibrosis in patients homozygous and heterozygous for delta F508 mutation
-
Johansen HK, Nir M, Høiby N, Koch C, Schwartz M. Severity of cystic fibrosis in patients homozygous and heterozygous for delta F508 mutation. Lancet. 1991;337(8742):631-634.
-
(1991)
Lancet
, vol.337
, Issue.8742
, pp. 631-634
-
-
Johansen, H.K.1
Nir, M.2
Høiby, N.3
Koch, C.4
Schwartz, M.5
-
13
-
-
0025241696
-
The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (delta F508)
-
Kerem E, Corey M, Kerem BS, et al. The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (delta F508). N Engl J Med. 1990;323(22):1517-1522.
-
(1990)
N Engl J Med
, vol.323
, Issue.22
, pp. 1517-1522
-
-
Kerem, E.1
Corey, M.2
Kerem, B.S.3
-
14
-
-
0028177981
-
DeltaF508 genotype does not predict disease severity in an ethnically diverse cystic fibrosis population
-
Lester LA, Kraut J, Lloyd-Still J, et al. Delta F508 genotype does not predict disease severity in an ethnically diverse cystic fibrosis population. Pediatrics. 1994;93(1):114-118. (Pubitemid 2037062)
-
(1994)
Pediatrics
, vol.93
, Issue.1
, pp. 114-118
-
-
Lester, L.A.1
Kraut, J.2
Lloyd-Still, J.3
Karrison, T.4
Mott, C.5
Billstrand, C.6
Lemke, A.7
Ober, C.8
-
15
-
-
0027517995
-
Correlation between genotype and phenotype in patients with cystic fibrosis
-
The Cystic Fibrosis Genotype-Phenotype Consortium
-
The Cystic Fibrosis Genotype-Phenotype Consortium. Correlation between genotype and phenotype in patients with cystic fibrosis. N Engl J Med. 1993;329(18):1308-1313.
-
(1993)
N Engl J Med
, vol.329
, Issue.18
, pp. 1308-1313
-
-
-
16
-
-
33751242495
-
CFTR genotype as a predictor of prognosis in cystic fibrosis
-
DOI 10.1378/chest.130.5.1441
-
McKone EF, Goss CH, Aitken ML. CFTR genotype as a predictor of prognosis in cystic fibrosis. Chest. 2006;130(5):1441-1447. (Pubitemid 44786738)
-
(2006)
Chest
, vol.130
, Issue.5
, pp. 1441-1447
-
-
McKone, E.F.1
Goss, C.H.2
Aitken, M.L.3
-
17
-
-
40549083327
-
Complex two-gene modulation of lung disease severity in children with cystic fibrosis
-
DOI 10.1172/JCI33754
-
Dorfman R, Sandford A, Taylor C, et al. Complex two-gene modulation of lung disease severity in children with cystic fibrosis. J Clin Invest. 2008;118(3):1040-1049. (Pubitemid 351364611)
-
(2008)
Journal of Clinical Investigation
, vol.118
, Issue.3
, pp. 1040-1049
-
-
Dorfman, R.1
Sandford, A.2
Taylor, C.3
Huang, B.4
Frangolias, D.5
Wang, Y.6
Sang, R.7
Pereira, L.8
Sun, L.9
Berthiaume, Y.10
Tsui, L.-C.11
Pare, P.D.12
Durie, P.13
Corey, M.14
Zielenski, J.15
-
18
-
-
25844491194
-
Genetic modifiers of lung disease in cystic fibrosis
-
Gene Modifier Study Group
-
Drumm ML, Konstan MW, Schluchter MD, et al; Gene Modifier Study Group. Genetic modifiers of lung disease in cystic fibrosis. N Engl J Med. 2005;353(14):1443-1453.
-
(2005)
N Engl J Med
, vol.353
, Issue.14
, pp. 1443-1453
-
-
Drumm, M.L.1
Konstan, M.W.2
Schluchter, M.D.3
-
19
-
-
0037323317
-
End-organ dysfunction in cystic fibrosis: Association with angiotensin I converting enzyme and cytokine gene polymorphisms
-
DOI 10.1164/rccm.200204-364OC
-
Arkwright PD, Pravica V, Geraghty PJ, et al. End-organ dysfunction in cystic fibrosis: association with angiotensin I converting enzyme and cytokine gene polymorphisms. Am J Respir Crit Care Med. 2003;167(3):384-389. (Pubitemid 36216420)
-
(2003)
American Journal of Respiratory and Critical Care Medicine
, vol.167
, Issue.3
, pp. 384-389
-
-
Arkwright, P.D.1
Pravica, V.2
Geraghty, P.J.3
Super, M.4
Webb, A.K.5
Schwarz, M.6
Hutchinson, I.V.7
-
20
-
-
0027278161
-
Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849+10 kb C→T mutation
-
DOI 10.1016/0140-6736(93)91885-P
-
Augarten A, Kerem BS, Yahav Y, et al. Mild cystic fibrosis and normal or borderline sweat test in patients with the 3849 + 10 kb C→T mutation. Lancet. 1993;342(8862):25-26. (Pubitemid 23183919)
-
(1993)
Lancet
, vol.342
, Issue.8862
, pp. 25-26
-
-
Augarten, A.1
Kerem, B.-S.2
Yahav, Y.3
Noiman, S.4
Rivlin, Y.5
Tal, A.6
Blau, H.7
Ben-Tur, L.8
Szeinberg, A.9
Kerem, E.10
Gazit, E.11
-
21
-
-
33644931158
-
Cystic fibrosis mutations with widely variable phenotype: The D1152H example
-
Mussaffi H, Prais D, Mei-Zahav M, Blau H. Cystic fibrosis mutations with widely variable phenotype: the D1152H example. Pediatr Pulmonol. 2006;41(3):250-254.
-
(2006)
Pediatr Pulmonol
, vol.41
, Issue.3
, pp. 250-254
-
-
Mussaffi, H.1
Prais, D.2
Mei-Zahav, M.3
Blau, H.4
-
22
-
-
1842603903
-
CFTR genotypes in patients with normal or borderline sweat chloride levels
-
Feldmann D, Couderc R, Audrezet MP, et al. CFTR genotypes in patients with normal or borderline sweat chloride levels. Hum Mutat. 2003;22(4):340.
-
(2003)
Hum Mutat
, vol.22
, Issue.4
, pp. 340
-
-
Feldmann, D.1
Couderc, R.2
Audrezet, M.P.3
-
23
-
-
0142074353
-
Nonclassic cystic fibrosis and CFTR-related diseases
-
Boyle MP. Nonclassic cystic fibrosis and CFTR-related diseases. Curr Opin Pulm Med. 2003;9(6):498-503. (Pubitemid 37268214)
-
(2003)
Current Opinion in Pulmonary Medicine
, vol.9
, Issue.6
, pp. 498-503
-
-
Boyle, M.P.1
-
24
-
-
47049115524
-
Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report
-
Cystic Fibrosis Foundation
-
Farrell PM, Rosenstein BJ, White TB, et al; Cystic Fibrosis Foundation. Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report. J Pediatr. 2008;153(2):S4-S14.
-
(2008)
J Pediatr
, vol.153
, Issue.2
-
-
Farrell, P.M.1
Rosenstein, B.J.2
White, T.B.3
-
25
-
-
0029016495
-
Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection
-
Demko CA, Byard PJ, Davis PB. Gender differences in cystic fibrosis: Pseudomonas aeruginosa infection. J Clin Epidemiol. 1995;48(8):1041-1049.
-
(1995)
J Clin Epidemiol
, vol.48
, Issue.8
, pp. 1041-1049
-
-
Demko, C.A.1
Byard, P.J.2
Davis, P.B.3
-
26
-
-
43249118265
-
Predictors of mucoid Pseudomonas colonization in cystic fibrosis patients
-
DOI 10.1002/ppul.20794
-
Levy H, Kalish LA, Cannon CL, et al. Predictors of mucoid Pseudomonas colonization in cystic fibrosis patients. Pediatr Pulmonol. 2008;43(5):463-471. (Pubitemid 351657313)
-
(2008)
Pediatric Pulmonology
, vol.43
, Issue.5
, pp. 463-471
-
-
Levy, H.1
Kalish, L.A.2
Cannon, C.L.3
Garcia, K.C.4
Gerard, C.5
Goldmann, D.6
Pier, G.B.7
Weiss, S.T.8
Colin, A.A.9
-
27
-
-
0030967472
-
Gender gap in cystic fibrosis mortality
-
Rosenfeld M, Davis R, FitzSimmons S, Pepe M, Ramsey B. Gender gap in cystic fibrosis mortality. Am J Epidemiol. 1997;145(9):794-803. (Pubitemid 27188516)
-
(1997)
American Journal of Epidemiology
, vol.145
, Issue.9
, pp. 794-803
-
-
Rosenfeld, M.1
Davis, R.2
Fitzsimmons, S.3
Pepe, M.4
Ramsey, B.5
-
28
-
-
27144501047
-
Is there still a gender gap in cystic fibrosis?
-
DOI 10.1378/chest.128.4.2824
-
Verma N, Bush A, Buchdahl R. Is there still a gender gap in cystic fibrosis? Chest. 2005;128(4):2824-2834. (Pubitemid 41507646)
-
(2005)
Chest
, vol.128
, Issue.4
, pp. 2824-2834
-
-
Verma, N.1
Bush, A.2
Buchdahl, R.3
-
29
-
-
0025181586
-
Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program
-
Waters DL, Dorney SF, Gaskin KJ, Gruca MA, O'Halloran M, Wilcken B. Pancreatic function in infants identified as having cystic fibrosis in a neonatal screening program. N Engl J Med. 1990;322(5):303-308. (Pubitemid 20046333)
-
(1990)
New England Journal of Medicine
, vol.322
, Issue.5
, pp. 303-308
-
-
Waters, D.L.1
Dorney, S.F.A.2
Gaskin, K.J.3
Gruca, M.A.4
O'Halloran, M.5
Wilcken, B.6
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