-
2
-
-
0024317145
-
DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis
-
Kerem B.S., Buchanan J.A., Durie P., et al. DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis. Am J Hum Genet 44 (1989) 827-834
-
(1989)
Am J Hum Genet
, vol.44
, pp. 827-834
-
-
Kerem, B.S.1
Buchanan, J.A.2
Durie, P.3
-
3
-
-
0034083024
-
Pancreatic aspects of cystic fibrosis and other inherited causes of pancreatic dysfunction
-
Durie P.R. Pancreatic aspects of cystic fibrosis and other inherited causes of pancreatic dysfunction. Med Clin North Am 84 (2000) 609-620
-
(2000)
Med Clin North Am
, vol.84
, pp. 609-620
-
-
Durie, P.R.1
-
4
-
-
0019131826
-
Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosis
-
Shepherd R., Cooksley W.G., and Cooke W.D. Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosis. J Pediatr 97 3 (1980) 351-357
-
(1980)
J Pediatr
, vol.97
, Issue.3
, pp. 351-357
-
-
Shepherd, R.1
Cooksley, W.G.2
Cooke, W.D.3
-
5
-
-
0022995617
-
Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease
-
Shepherd R.W., Holt T.L., Thomas B.J., et al. Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease. J Pediatr 109 5 (1986) 788-794
-
(1986)
J Pediatr
, vol.109
, Issue.5
, pp. 788-794
-
-
Shepherd, R.W.1
Holt, T.L.2
Thomas, B.J.3
-
6
-
-
0026666330
-
Malnutrition and age-specific nutritional management in cystic fibrosis
-
Dodge J.A. Malnutrition and age-specific nutritional management in cystic fibrosis. Neth J Med 41 3-4 (1992) 127-129
-
(1992)
Neth J Med
, vol.41
, Issue.3-4
, pp. 127-129
-
-
Dodge, J.A.1
-
7
-
-
0029101397
-
Nutritional growth retardation is associated with defective lung growth in cystic fibrosis: a preventable determinant of progressive pulmonary dysfunction
-
Thomson M.A., Quirk P., Swanson C.E., et al. Nutritional growth retardation is associated with defective lung growth in cystic fibrosis: a preventable determinant of progressive pulmonary dysfunction. Nutrition 11 4 (1995) 350-354
-
(1995)
Nutrition
, vol.11
, Issue.4
, pp. 350-354
-
-
Thomson, M.A.1
Quirk, P.2
Swanson, C.E.3
-
8
-
-
0033669816
-
Pathogenesis of malnutrition in cystic fibrosis, and its treatment
-
Pencharz P.B., and Durie P.R. Pathogenesis of malnutrition in cystic fibrosis, and its treatment. Clin Nutr 19 6 (2000) 387-394
-
(2000)
Clin Nutr
, vol.19
, Issue.6
, pp. 387-394
-
-
Pencharz, P.B.1
Durie, P.R.2
-
9
-
-
0033827478
-
Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry
-
Zemel B.S., Jawad A.F., FitzSimmons S., and Stallings V.A. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry. J Pediatr 137 3 (2000 Sep) 374-380
-
(2000)
J Pediatr
, vol.137
, Issue.3
, pp. 374-380
-
-
Zemel, B.S.1
Jawad, A.F.2
FitzSimmons, S.3
Stallings, V.A.4
-
10
-
-
0036311232
-
Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project
-
Steinkamp G., and Wiedemann B. Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project. Thorax 57 7 (2002) 596-601
-
(2002)
Thorax
, vol.57
, Issue.7
, pp. 596-601
-
-
Steinkamp, G.1
Wiedemann, B.2
-
11
-
-
0037795302
-
Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis
-
Konstan M.W., Butler S.M., Wohl M.E., et al. Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis. J Pediatr 142 6 (2003) 624-630
-
(2003)
J Pediatr
, vol.142
, Issue.6
, pp. 624-630
-
-
Konstan, M.W.1
Butler, S.M.2
Wohl, M.E.3
-
12
-
-
0027395872
-
The changing epidemiology of cystic fibrosis
-
FitzSimmons S.C. The changing epidemiology of cystic fibrosis. J Pediatr 122 1 (1993) 1-9
-
(1993)
J Pediatr
, vol.122
, Issue.1
, pp. 1-9
-
-
FitzSimmons, S.C.1
-
13
-
-
0003926985
-
-
Cystic Fibrosis Foundation Patient Registry, Bethesda, Maryland
-
Cystic Fibrosis Foundation Patient Registry. Annual Data Report (2007), Bethesda, Maryland
-
(2007)
Annual Data Report
-
-
-
14
-
-
0023836170
-
Study to compare the enzyme activity, acid resistance and dissolution characteristics of currently available pancreatic enzyme preparations
-
Whitehead A.M. Study to compare the enzyme activity, acid resistance and dissolution characteristics of currently available pancreatic enzyme preparations. Pharm Weekbl Sci 10 1 (1988) 12-16
-
(1988)
Pharm Weekbl Sci
, vol.10
, Issue.1
, pp. 12-16
-
-
Whitehead, A.M.1
-
15
-
-
0028332006
-
Clinical pharmacology of pancreatic enzymes in patients with cystic fibrosis and in vitro performance of microencapsulated formulations
-
Kraisinger M., Hochhaus G., Stecenko A., Bowser E., and Hendeles L. Clinical pharmacology of pancreatic enzymes in patients with cystic fibrosis and in vitro performance of microencapsulated formulations. J Clin Pharmacol 34 2 (1994) 158-166
-
(1994)
J Clin Pharmacol
, vol.34
, Issue.2
, pp. 158-166
-
-
Kraisinger, M.1
Hochhaus, G.2
Stecenko, A.3
Bowser, E.4
Hendeles, L.5
-
16
-
-
14244268571
-
Enzyme content and acid stability of enteric-coated pancreatic enzyme products in vitro
-
Case C.L., Henniges F., and Barkin J.S. Enzyme content and acid stability of enteric-coated pancreatic enzyme products in vitro. Pancreas 30 2 (2005) 180-183
-
(2005)
Pancreas
, vol.30
, Issue.2
, pp. 180-183
-
-
Case, C.L.1
Henniges, F.2
Barkin, J.S.3
-
17
-
-
13444252444
-
Gastrointestinal outcomes and confounders in cystic fibrosis
-
Borowitz D., Durie P.R., Clarke L.L., et al. Gastrointestinal outcomes and confounders in cystic fibrosis. J Pediatr 146 2 (2005) 189-193
-
(2005)
J Pediatr
, vol.146
, Issue.2
, pp. 189-193
-
-
Borowitz, D.1
Durie, P.R.2
Clarke, L.L.3
-
18
-
-
0028827338
-
Fibrosing colonopathy in cystic fibrosis: results of a case-control study
-
Smyth R.L., Ashby D., O'Hea U., et al. Fibrosing colonopathy in cystic fibrosis: results of a case-control study. Lancet 346 (1995) 1247-1251
-
(1995)
Lancet
, vol.346
, pp. 1247-1251
-
-
Smyth, R.L.1
Ashby, D.2
O'Hea, U.3
-
19
-
-
0030782086
-
Patterns of use of pancreatic enzyme supplements in fibrosing colonopathy: implications for pathogenesis
-
Bakowski M.T., and Prescott P. Patterns of use of pancreatic enzyme supplements in fibrosing colonopathy: implications for pathogenesis. Pharmacoepidemiol Drug Saf 6 (1997) 347-358
-
(1997)
Pharmacoepidemiol Drug Saf
, vol.6
, pp. 347-358
-
-
Bakowski, M.T.1
Prescott, P.2
-
20
-
-
0030905117
-
High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis
-
FitzSimmons S.C., Burkhart G.A., Borowitz D., et al. High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis. N Engl J Med 336 (1997) 1283-1289
-
(1997)
N Engl J Med
, vol.336
, pp. 1283-1289
-
-
FitzSimmons, S.C.1
Burkhart, G.A.2
Borowitz, D.3
-
21
-
-
70450221785
-
-
Center for Drug Evaluation and Research. Guidance for industry: exocrine pancreatic insufficiency drug products-submitting NDAs. April, Available at:, Accessed June 27, 2008
-
U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for industry: exocrine pancreatic insufficiency drug products-submitting NDAs. April 2006. Available at: http://www.fda.gov/cder/guidance/6275fnl.htm. Accessed June 27, 2008.
-
(2006)
-
-
-
22
-
-
0023106926
-
Pancreatic enzyme supplementation as acid-resistant microspheres versus enteric-coated granules in cystic fibrosis. A double placebo controlled cross-over study
-
Petersen W., Heilmann C., and Garne S. Pancreatic enzyme supplementation as acid-resistant microspheres versus enteric-coated granules in cystic fibrosis. A double placebo controlled cross-over study. Acta Paediatr Scand 76 (1987) 66-69
-
(1987)
Acta Paediatr Scand
, vol.76
, pp. 66-69
-
-
Petersen, W.1
Heilmann, C.2
Garne, S.3
-
23
-
-
0024488402
-
High compared with standard dose lipase pancreatic supplement
-
Robinson P.J., Olinsky A., Smith A.L., et al. High compared with standard dose lipase pancreatic supplement. Arch Dis Child 64 (1989) 143-145
-
(1989)
Arch Dis Child
, vol.64
, pp. 143-145
-
-
Robinson, P.J.1
Olinsky, A.2
Smith, A.L.3
-
24
-
-
0026761748
-
Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosis
-
Morrison G., Morrison J.M., Redmond A.O., et al. Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosis. Aliment Pharmacol Ther 6 (1992) 549-555
-
(1992)
Aliment Pharmacol Ther
, vol.6
, pp. 549-555
-
-
Morrison, G.1
Morrison, J.M.2
Redmond, A.O.3
-
25
-
-
0027983501
-
Comparison of weight-based dosages of enteric-coated microtablet enzyme preparations in patients with cystic fibrosis
-
Beker L.T., Fink R.J., Shamsa F.H., et al. Comparison of weight-based dosages of enteric-coated microtablet enzyme preparations in patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 19 (1994) 191-197
-
(1994)
J Pediatr Gastroenterol Nutr
, vol.19
, pp. 191-197
-
-
Beker, L.T.1
Fink, R.J.2
Shamsa, F.H.3
-
26
-
-
0036900686
-
Creon 10,000 minimicrospheres vs. Creon 8,000 microspheres-an open randomised crossover preference study
-
Patchell C.J., Desai M., Weller P.H., et al. Creon 10,000 minimicrospheres vs. Creon 8,000 microspheres-an open randomised crossover preference study. J Cyst Fibros 1 4 (2002) 287-291
-
(2002)
J Cyst Fibros
, vol.1
, Issue.4
, pp. 287-291
-
-
Patchell, C.J.1
Desai, M.2
Weller, P.H.3
-
27
-
-
0028885145
-
Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy, Consensus Committee
-
Borowitz D.S., Grand R.J., and Durie P.R. Use of pancreatic enzyme supplements for patients with cystic fibrosis in the context of fibrosing colonopathy, Consensus Committee. J Pediatr 127 (1995) 681-684
-
(1995)
J Pediatr
, vol.127
, pp. 681-684
-
-
Borowitz, D.S.1
Grand, R.J.2
Durie, P.R.3
-
28
-
-
0036735017
-
Consensus report on nutrition for pediatric patients with cystic fibrosis
-
Borowitz D., Baker R.D., and Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 35 (2002) 246-259
-
(2002)
J Pediatr Gastroenterol Nutr
, vol.35
, pp. 246-259
-
-
Borowitz, D.1
Baker, R.D.2
Stallings, V.3
-
29
-
-
0345119248
-
Gastric, pancreatic, and intestinal function
-
Burtis C.A., and Ashwood E.R. (Eds), WB Saunders, Philadelphia
-
Henderson A.R., and Rinker A.D. Gastric, pancreatic, and intestinal function. In: Burtis C.A., and Ashwood E.R. (Eds). Tietz textbook of clinical chemistry. 3rd ed (1999), WB Saunders, Philadelphia 1293-1295
-
(1999)
Tietz textbook of clinical chemistry. 3rd ed
, pp. 1293-1295
-
-
Henderson, A.R.1
Rinker, A.D.2
-
30
-
-
0028022699
-
Steatocrit: a reliable semiquantitative method for detection of steatorrhea
-
Sugai E., Srur G., Vazquez H., et al. Steatocrit: a reliable semiquantitative method for detection of steatorrhea. J Clin Gastroenterol 19 3 (1994) 206-209
-
(1994)
J Clin Gastroenterol
, vol.19
, Issue.3
, pp. 206-209
-
-
Sugai, E.1
Srur, G.2
Vazquez, H.3
-
33
-
-
0242404303
-
Lipid, nitrogen, water and energy content of a single stool sample in healthy children and children with cystic fibrosis
-
Van den Neucker A.M., Forget P.P., and van Kreel B. Lipid, nitrogen, water and energy content of a single stool sample in healthy children and children with cystic fibrosis. Eur J Pediatr 162 11 (2003) 764-766
-
(2003)
Eur J Pediatr
, vol.162
, Issue.11
, pp. 764-766
-
-
Van den Neucker, A.M.1
Forget, P.P.2
van Kreel, B.3
-
34
-
-
0027057788
-
Fecal fat concentration in the screening of steatorrhea
-
Benini L., Caliari S., Bonfante F., et al. Fecal fat concentration in the screening of steatorrhea. Digestion 53 1-2 (1992) 94-100
-
(1992)
Digestion
, vol.53
, Issue.1-2
, pp. 94-100
-
-
Benini, L.1
Caliari, S.2
Bonfante, F.3
-
35
-
-
0030732216
-
Acid steatocrit: a simple, rapid gravimetric method to determine steatorrhea
-
Amann S.T., Josephson S.A., and Toskes P.P. Acid steatocrit: a simple, rapid gravimetric method to determine steatorrhea. Am J Gastroenterol 92 12 (1997) 2280-2284
-
(1997)
Am J Gastroenterol
, vol.92
, Issue.12
, pp. 2280-2284
-
-
Amann, S.T.1
Josephson, S.A.2
Toskes, P.P.3
-
38
-
-
27644550517
-
Update on the evaluation of pancreatic exocrine status in cystic fibrosis
-
Borowitz D. Update on the evaluation of pancreatic exocrine status in cystic fibrosis. Curr Opin Pulm Med 11 6 (2005) 524-527
-
(2005)
Curr Opin Pulm Med
, vol.11
, Issue.6
, pp. 524-527
-
-
Borowitz, D.1
-
39
-
-
0034094974
-
Control of malabsorption in cystic fibrosis
-
Littlewood J.M., and Wolfe S.P. Control of malabsorption in cystic fibrosis. Paediatr Drugs 2 3 (2000) 205-222
-
(2000)
Paediatr Drugs
, vol.2
, Issue.3
, pp. 205-222
-
-
Littlewood, J.M.1
Wolfe, S.P.2
-
40
-
-
0020333990
-
Comparison of effectiveness of pancreatic enzyme preparations in cystic fibrosis
-
Mischler E.H., Parrell S., Farrell P.M., and Odell G.B. Comparison of effectiveness of pancreatic enzyme preparations in cystic fibrosis. Am J Dis Child 136 (1982) 1060-1063
-
(1982)
Am J Dis Child
, vol.136
, pp. 1060-1063
-
-
Mischler, E.H.1
Parrell, S.2
Farrell, P.M.3
Odell, G.B.4
-
41
-
-
11144346971
-
Ultrase MT12 and Ultrase MT20 in the treatment of exocrine pancreatic insufficiency in cystic fibrosis: safety and efficacy
-
Konstan M.W., Stern R.C., Trout J.R., et al. Ultrase MT12 and Ultrase MT20 in the treatment of exocrine pancreatic insufficiency in cystic fibrosis: safety and efficacy. Aliment Pharmacol Ther 20 (2004) 1365-1371
-
(2004)
Aliment Pharmacol Ther
, vol.20
, pp. 1365-1371
-
-
Konstan, M.W.1
Stern, R.C.2
Trout, J.R.3
-
42
-
-
0033897668
-
A comparison of the efficacy and tolerance of pancrelipase and placebo in the treatment of steatorrhea in cystic fibrosis patients with clinical exocrine pancreatic insufficiency
-
Stern R.C., Eisenberg J.D., Wagener J.S., et al. A comparison of the efficacy and tolerance of pancrelipase and placebo in the treatment of steatorrhea in cystic fibrosis patients with clinical exocrine pancreatic insufficiency. Am J Gastroenterol 95 (2000) 1932-1938
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 1932-1938
-
-
Stern, R.C.1
Eisenberg, J.D.2
Wagener, J.S.3
-
43
-
-
33746089930
-
An enteric-coated high-buffered pancrelipase reduces steatorrhea in patients with cystic fibrosis: a prospective, randomized study
-
Brady M.S., Garson J.L., Krug S.K., et al. An enteric-coated high-buffered pancrelipase reduces steatorrhea in patients with cystic fibrosis: a prospective, randomized study. J Am Diet Assoc 106 8 (2006) 1181-1186
-
(2006)
J Am Diet Assoc
, vol.106
, Issue.8
, pp. 1181-1186
-
-
Brady, M.S.1
Garson, J.L.2
Krug, S.K.3
-
44
-
-
33751119814
-
Study of a novel pancreatic enzyme replacement therapy in pancreatic insufficient subjects with cystic fibrosis
-
Borowitz D., Goss C.H., Limauro S., et al. Study of a novel pancreatic enzyme replacement therapy in pancreatic insufficient subjects with cystic fibrosis. J Pediatr 149 5 (2006) 658-662
-
(2006)
J Pediatr
, vol.149
, Issue.5
, pp. 658-662
-
-
Borowitz, D.1
Goss, C.H.2
Limauro, S.3
|