-
1
-
-
0026526840
-
Cystic fibrosis: Beyond the gene to therapy
-
Tizzano EF, Buchwald M. Cystic fibrosis: beyond the gene to therapy. J Pediatr 1992;120:337-49.
-
(1992)
J Pediatr
, vol.120
, pp. 337-349
-
-
Tizzano, E.F.1
Buchwald, M.2
-
3
-
-
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: 1073-80.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
-
4
-
-
0025314653
-
Statement on population screening for the cystic fibrosis gene
-
National Institutes of Health. Statement on population screening for the cystic fibrosis gene. N Engl J Med 1990;323:70-1.
-
(1990)
N Engl J Med
, vol.323
, pp. 70-71
-
-
-
6
-
-
15844428786
-
-
Toronto: Canadian Cystic Fibrosis Foundation
-
Canadian Cystic Fibrosis Foundation. Report of the Canadian Patient Data Registry 1992. Toronto: Canadian Cystic Fibrosis Foundation, 1994.
-
(1994)
Report of the Canadian Patient Data Registry 1992
-
-
-
7
-
-
15844379208
-
-
Ottawa: Statistics Canada, Statistics Canada catalogue no. 11-402E
-
Statistics Canada. Canada year book 1990. Ottawa: Statistics Canada, 1990. (Statistics Canada catalogue no. 11-402E).
-
(1990)
Canada Year Book 1990
-
-
-
8
-
-
85035171091
-
-
Health Reports
-
Statistics Canada. Births 1989. Health Reports, suppl no. 14, 1991.
-
(1991)
Births 1989
, Issue.14 SUPPL.
-
-
-
9
-
-
15844411366
-
-
Ottawa: Statistics Canada
-
Statistics Canada. Causes of death 1965-1989. Ottawa: Statistics Canada, 1967-1991.
-
(1967)
Causes of Death 1965-1989
-
-
-
10
-
-
33845382806
-
Nonparametric estimation from incomplete observations
-
Kaplan EL, Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc 1958;53:457-81.
-
(1958)
J Am Stat Assoc
, vol.53
, pp. 457-481
-
-
Kaplan, E.L.1
Meier, P.2
-
11
-
-
0000336139
-
Regression models and life-tables
-
Cox DR. Regression models and life-tables (with discussion). J R Stat Soc [B] 1972;34:187-220.
-
(1972)
J R Stat Soc [B]
, vol.34
, pp. 187-220
-
-
Cox, D.R.1
-
12
-
-
0017097945
-
Five to seven year course of pulmonary function in cystic fibrosis
-
Corey M, Levison H, Crozier D. Five to seven year course of pulmonary function in cystic fibrosis. Am Rev Respir Dis 1976;114:1085-92.
-
(1976)
Am Rev Respir Dis
, vol.114
, pp. 1085-1092
-
-
Corey, M.1
Levison, H.2
Crozier, D.3
-
13
-
-
0013977629
-
Standards from birth to maturity for height, weight, height velocity and weight velocity
-
Tanner JM, Whitehouse RH, Takaishi M. Standards from birth to maturity for height, weight, height velocity and weight velocity. Arch Dis Child 1966;41:613-35.
-
(1966)
Arch Dis Child
, vol.41
, pp. 613-635
-
-
Tanner, J.M.1
Whitehouse, R.H.2
Takaishi, M.3
-
14
-
-
0019366004
-
The pathogenesis and treatment of pulmonary infections in patients with cystic fibrosis
-
Marks MI. The pathogenesis and treatment of pulmonary infections in patients with cystic fibrosis. J Pediatr 1981;98: 173-9.
-
(1981)
J Pediatr
, vol.98
, pp. 173-179
-
-
Marks, M.I.1
-
15
-
-
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;104:206-10.
-
(1984)
J Pediatr
, vol.104
, pp. 206-210
-
-
Isles, A.1
Maclusky, I.2
Corey, M.3
-
20
-
-
0020070795
-
Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption
-
Gaskin K, Gurwitz D, Durie P, et al. Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. J Pediatr 1982;100:857-62.
-
(1982)
J Pediatr
, vol.100
, pp. 857-862
-
-
Gaskin, K.1
Gurwitz, D.2
Durie, P.3
-
21
-
-
0026520359
-
Prediction of mortality in patients with cystic fibrosis
-
Kerem E, Reisman J, Corey M, et al. Prediction of mortality in patients with cystic fibrosis. N Engl J Med 1992;326: 1187-91.
-
(1992)
N Engl J Med
, vol.326
, pp. 1187-1191
-
-
Kerem, E.1
Reisman, J.2
Corey, M.3
-
22
-
-
0026532741
-
Cystic fibrosis mutations in French Canadians: Three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis
-
Rozen R, De Braekeleer M, Daigneault J, et al. Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis. Am J Med Genet 1992;42:360-4.
-
(1992)
Am J Med Genet
, vol.42
, pp. 360-364
-
-
Rozen, R.1
De Braekeleer, M.2
Daigneault, J.3
-
23
-
-
0026734588
-
Genetic determination of exocrine pancreatic function in cystic fibrosis
-
Kristidis P, Bozon D, Corey M, et al. Genetic determination of exocrine pancreatic function in cystic fibrosis. Am J Hum Genet 1992;50:1178-84.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1178-1184
-
-
Kristidis, P.1
Bozon, D.2
Corey, M.3
-
24
-
-
0016272002
-
Cystic fibrosis: A not-so-fatal disease
-
Crozier DN. Cystic fibrosis: a not-so-fatal disease. Pediatr Clin North Am 1974;21:935-50.
-
(1974)
Pediatr Clin North Am
, vol.21
, pp. 935-950
-
-
Crozier, D.N.1
-
25
-
-
0026541404
-
Nutritional support and management in cystic fibrosis: A consensus report
-
Ramsey BW, Farrell PM, Pencharz P, and the Consensus Committee. Nutritional support and management in cystic fibrosis: a consensus report. Am J Clin Nutr 1992;55:108-16.
-
(1992)
Am J Clin Nutr
, vol.55
, pp. 108-116
-
-
Ramsey, B.W.1
Farrell, P.M.2
Pencharz, P.3
-
26
-
-
0020564247
-
Energy intakes and low-fat diets in children with cystic fibrosis
-
Pencharz PB. Energy intakes and low-fat diets in children with cystic fibrosis. (Editorial). J Pediatr Gastroenterol 1983;2: 400-2.
-
(1983)
J Pediatr Gastroenterol
, vol.2
, pp. 400-402
-
-
Pencharz, P.B.1
-
27
-
-
0027395872
-
The changing epidemiology of cystic fibrosis
-
Fitzsimmons SC. The changing epidemiology of cystic fibrosis. J Pediatr 1993:122:1-9.
-
(1993)
J Pediatr
, vol.122
, pp. 1-9
-
-
Fitzsimmons, S.C.1
-
28
-
-
0024599433
-
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus
-
Kerem E, Corey M, Durie P, et al. Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus. J Pediatr 1989;114:767-73.
-
(1989)
J Pediatr
, vol.114
, pp. 767-773
-
-
Kerem, E.1
Corey, M.2
Durie, P.3
-
29
-
-
0027173169
-
Cystic fibrosis in the United Kingdom, 1968-88: Incidence, population and survival
-
Dodge JA, Morison S, Lewis PA, et al. Cystic fibrosis in the United Kingdom, 1968-88: incidence, population and survival. Paediatr Perinatal Epidemiol 1993;7:157-66.
-
(1993)
Paediatr Perinatal Epidemiol
, vol.7
, pp. 157-166
-
-
Dodge, J.A.1
Morison, S.2
Lewis, P.A.3
-
30
-
-
0023409238
-
Are age, sex, age at diagnosis, or mode of presentation prognostic factors for cystic fibrosis?
-
Hudson I, Phelan PD. Are age, sex, age at diagnosis, or mode of presentation prognostic factors for cystic fibrosis? Pediatr Pulmonol 1987;3:288-97.
-
(1987)
Pediatr Pulmonol
, vol.3
, pp. 288-297
-
-
Hudson, I.1
Phelan, P.D.2
-
31
-
-
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;82:871-9.
-
(1987)
Am J Med
, vol.82
, pp. 871-879
-
-
Huang, N.N.1
Schidlow, D.V.2
Szatrowski, T.H.3
-
32
-
-
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; 41:583-91.
-
(1988)
J Clin Epidemiol
, vol.41
, pp. 583-591
-
-
Corey, M.1
McLaughlin, F.J.2
Williams, M.3
-
33
-
-
0023556435
-
Management of Pseudomonas aeruginosa lung infection in Danish cystic fibrosis patients
-
Pedersen SS, Jensen T, Hoiby N, et al. Management of Pseudomonas aeruginosa lung infection in Danish cystic fibrosis patients. Acta Paediatr Scand 1987;76:955-61.
-
(1987)
Acta Paediatr Scand
, vol.76
, pp. 955-961
-
-
Pedersen, S.S.1
Jensen, T.2
Hoiby, N.3
-
34
-
-
0025355607
-
Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa
-
Kerem E, Corey M, Gold R, et al. Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa. J Pediatr 1990; 116:714-19.
-
(1990)
J Pediatr
, vol.116
, pp. 714-719
-
-
Kerem, E.1
Corey, M.2
Gold, R.3
-
35
-
-
0025013016
-
Effect of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients
-
Lewin LO, Byard PJ, Davis PB. Effect of Pseudomonas cepacia colonization on survival and pulmonary function of cystic fibrosis patients. J Clin Epidemiol 1990;43:125-31.
-
(1990)
J Clin Epidemiol
, vol.43
, pp. 125-131
-
-
Lewin, L.O.1
Byard, P.J.2
Davis, P.B.3
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