-
1
-
-
0025982350
-
Exercise performance and breathing patterns in cystic fibrosis: Male-female differences and the influence of resting pulmonary function
-
Orenstein DM, Nixon PA. Exercise performance and breathing patterns in cystic fibrosis: male-female differences and the influence of resting pulmonary function. Pediatr Pulmonol 1991; 10:101-05
-
(1991)
Pediatr Pulmonol
, vol.10
, pp. 101-105
-
-
Orenstein, D.M.1
Nixon, P.A.2
-
2
-
-
0027494891
-
Endurance exercise capacity in adults with cystic fibrosis
-
Freeman W, Stableforth DE, Cayton RM, et al. Endurance exercise capacity in adults with cystic fibrosis. Respir Med 1993; 87:541-49
-
(1993)
Respir Med
, vol.87
, pp. 541-549
-
-
Freeman, W.1
Stableforth, D.E.2
Cayton, R.M.3
-
3
-
-
0026732845
-
Analysis of factors limiting maximal exercise performance in cystic fibrosis
-
Lands LC, Heigenhauser JF, Jones NL. Analysis of factors limiting maximal exercise performance in cystic fibrosis. Clin Sci 1992; 83:391-97
-
(1992)
Clin Sci
, vol.83
, pp. 391-397
-
-
Lands, L.C.1
Heigenhauser, J.F.2
Jones, N.L.3
-
4
-
-
0022778966
-
Multiple factors limit exercise capacity in cystic fibrosis
-
Marcotte JE, Grisdale BA, Levison H, et al. Multiple factors limit exercise capacity in cystic fibrosis. Pediatr Pulmonol 1986; 2:274-81
-
(1986)
Pediatr Pulmonol
, vol.2
, pp. 274-281
-
-
Marcotte, J.E.1
Grisdale, B.A.2
Levison, H.3
-
5
-
-
0015043620
-
Pulmonary function and response to exercise in cystic fibrosis
-
Godfrey S, Mearns M. Pulmonary function and response to exercise in cystic fibrosis. Arch Dis Child 1971; 46:144-51
-
(1971)
Arch Dis Child
, vol.46
, pp. 144-151
-
-
Godfrey, S.1
Mearns, M.2
-
6
-
-
0018865171
-
The role of nutritional status, airway obstruction, hypoxia and abnormalities of serum lipid composition in limiting exercise tolerance in children with cystic fibrosis
-
Coates AL, Boyee P, Muller D, et al. The role of nutritional status, airway obstruction, hypoxia and abnormalities of serum lipid composition in limiting exercise tolerance in children with cystic fibrosis. Acta Paediatr Scand 1980; 69:353-58
-
(1980)
Acta Paediatr Scand
, vol.69
, pp. 353-358
-
-
Coates, A.L.1
Boyee, P.2
Muller, D.3
-
7
-
-
0017097945
-
Five- to 7-year course of pulmonary function in cystic fibrosis
-
Corey M, Levison H, Crozier D. Five- to 7-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
-
8
-
-
0023268189
-
Cystic fibrosis in adolescents and adults
-
Penketh ARL, Wise A, Mearns MB, et al. Cystic fibrosis in adolescents and adults. Thorax 1987; 42:526-32
-
(1987)
Thorax
, vol.42
, pp. 526-532
-
-
Penketh, A.R.L.1
Wise, A.2
Mearns, M.B.3
-
9
-
-
0025013016
-
Effect of Pseudomonas cepacia colonisation on survival and pulmonary function of cystic fibrosis patients
-
Lewin LO, Byard PJ, Davies BD. Effect of Pseudomonas cepacia colonisation 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
Davies, B.D.3
-
10
-
-
0020585150
-
Changes in the normal maximum expiratory flow-volume curve with growth and ageing
-
Knudson RJ, Lebowitz MD, Hollberg CJ, et al. Changes in the normal maximum expiratory flow-volume curve with growth and ageing. Am Rev Respir Dis 1983; 127:725-34
-
(1983)
Am Rev Respir Dis
, vol.127
, pp. 725-734
-
-
Knudson, R.J.1
Lebowitz, M.D.2
Hollberg, C.J.3
-
13
-
-
0023753168
-
The natural history of forced expiratory volumes: Effect of cigarette smoking and respiratory symptoms
-
Tager IB, Segal MR, Speizer FE, et al. The natural history of forced expiratory volumes: effect of cigarette smoking and respiratory symptoms. Am Rev Respir Dis 1988; 138:837-49
-
(1988)
Am Rev Respir Dis
, vol.138
, pp. 837-849
-
-
Tager, I.B.1
Segal, M.R.2
Speizer, F.E.3
-
14
-
-
0024437991
-
On temporal relations between lung function and somatic growth
-
Sherril DL, Camilli A, Lebowitz MD. On temporal relations between lung function and somatic growth. Am Rev Respir Dis 1989; 140:638-44
-
(1989)
Am Rev Respir Dis
, vol.140
, pp. 638-644
-
-
Sherril, D.L.1
Camilli, A.2
Lebowitz, M.D.3
-
15
-
-
0028438616
-
The adolescent growth spurt in children with cystic fibrosis
-
Byard PJ. The adolescent growth spurt in children with cystic fibrosis. Ann Hum Biol 1994; 21:229-40
-
(1994)
Ann Hum Biol
, vol.21
, pp. 229-240
-
-
Byard, P.J.1
-
16
-
-
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
-
18
-
-
0017843165
-
Relative underweight in cystic fibrosis and it's prognostic value
-
Kraemer R, Rudeberg A, Hadorn B, et al. Relative underweight in cystic fibrosis and it's prognostic value. Acta Paediatr Scand 1978; 67:33-7
-
(1978)
Acta Paediatr Scand
, vol.67
, pp. 33-37
-
-
Kraemer, R.1
Rudeberg, A.2
Hadorn, B.3
-
19
-
-
0023425424
-
Energy expenditure of patients with cystic fibrosis
-
Vaisman N, Pencharz PB, Corey M, et al. Energy expenditure of patients with cystic fibrosis. J Pediatr 1987; 111:496-99
-
(1987)
J Pediatr
, vol.111
, pp. 496-499
-
-
Vaisman, N.1
Pencharz, P.B.2
Corey, M.3
-
20
-
-
0020070795
-
Improved respiratory prognosis in patients with normal fat absorption
-
Gaskin K, Gurwitz D, Durie P, et al. Improved respiratory prognosis in patients 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
-
-
0025720681
-
The cystic fibrosis gene and resting energy expenditure
-
Fried MD, Durie PR, Tsui L, et al. The cystic fibrosis gene and resting energy expenditure. J Pediatr 1991; 119:913-16
-
(1991)
J Pediatr
, vol.119
, pp. 913-916
-
-
Fried, M.D.1
Durie, P.R.2
Tsui, L.3
-
23
-
-
0026651569
-
Eight-year follow-up of pulmonary function and oxygen uptake during exercise in 16-year-old males with cystic fibrosis
-
Stranghelle JK, Skyberg D, Haanaes OC. Eight-year follow-up of pulmonary function and oxygen uptake during exercise in 16-year-old males with cystic fibrosis. Acta Paediatr Scand 1992; 81:527-31
-
(1992)
Acta Paediatr Scand
, vol.81
, pp. 527-531
-
-
Stranghelle, J.K.1
Skyberg, D.2
Haanaes, O.C.3
-
24
-
-
0004240703
-
-
Bethesda, Md: Cystic Fibrosis Foundation, August
-
Cystic Fibrosis Foundation. Patient registry 1994 annual data report. Bethesda, Md: Cystic Fibrosis Foundation, August 1995
-
(1995)
Patient Registry 1994 Annual Data Report
-
-
-
25
-
-
0019487340
-
Exercise conditioning and cardiopulmonary fitness in cystic fibrosis: The effects of a 3 month supervised running program
-
Orenstein DM, Franklin BA, Doershuk CF, et al. Exercise conditioning and cardiopulmonary fitness in cystic fibrosis: the effects of a 3 month supervised running program. Chest 1981; 80:392-98
-
(1981)
Chest
, vol.80
, pp. 392-398
-
-
Orenstein, D.M.1
Franklin, B.A.2
Doershuk, C.F.3
-
26
-
-
0022495599
-
Effects of a swimming program on children with cystic fibrosis
-
Edlund LD, French RW, Herbst JJ, et al. Effects of a swimming program on children with cystic fibrosis. Am J Dis Child 1986; 140:80-3
-
(1986)
Am J Dis Child
, vol.140
, pp. 80-83
-
-
Edlund, L.D.1
French, R.W.2
Herbst, J.J.3
-
27
-
-
0024844327
-
Effects of exercise and physiotherapy in aiding sputum expectoration in adults with cystic fibrosis
-
Sahl W, Bilton D, Dodd M, et al. Effects of exercise and physiotherapy in aiding sputum expectoration in adults with cystic fibrosis. Thorax 1989; 44:1006-08
-
(1989)
Thorax
, vol.44
, pp. 1006-1008
-
-
Sahl, W.1
Bilton, D.2
Dodd, M.3
|