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Frequency of the delta F508 mutation on cystic fibrosis chromosomes in Denmark.
Schwartz M, Johansen HK, Koch C, Brandt NJ. Schwartz M, et al. Among authors: koch c. Hum Genet. 1990 Sep;85(4):427-8. doi: 10.1007/BF02428297. Hum Genet. 1990. PMID: 2210762
The majority of the chromosomes with this mutation are found on chromosomes with the XV2c/KM19 haplotype B (97.3%), whereas 15/16 chromosomes with haplotype C have another mutation, confirming that only very few mutations will account for the majority of CF genes in the Da …
The majority of the chromosomes with this mutation are found on chromosomes with the XV2c/KM19 haplotype B (97.3%), whereas 15/16 chromosome …
Cushing's syndrome due to pharmacological interaction in a cystic fibrosis patient.
Main KM, Skov M, Sillesen IB, Dige-Petersen H, Müller J, Koch C, Lanng S. Main KM, et al. Among authors: koch c. Acta Paediatr. 2002;91(9):1008-11. doi: 10.1080/080352502760272759. Acta Paediatr. 2002. PMID: 12412882
Specific IgG2 antibodies to Pseudomonas aeruginosa lipid A and lipopolysaccharide are early markers of chronic infection in patients with cystic fibrosis.
Kronborg G, Pressler T, Fomsgaard A, Koch C, Høiby N. Kronborg G, et al. Among authors: koch c. Infection. 1993 Sep-Oct;21(5):297-302. doi: 10.1007/BF01712448. Infection. 1993. PMID: 8300245
Proinsulin, insulin, and C-peptide in cystic fibrosis after an oral glucose tolerance test.
Hartling SG, Garne S, Binder C, Heilmann C, Petersen W, Petersen KE, Koch C. Hartling SG, et al. Among authors: koch c. Diabetes Res. 1988 Apr;7(4):165-9. Diabetes Res. 1988. PMID: 3042255
The beta-cell response to an oral glucose load was studied in 22 patients with cystic fibrosis (CF) by means of insulin, C-peptide and proinsulin, and the results compared with those from 20 healthy sex and age matched controls. ...All patients showed lower insulin and …
The beta-cell response to an oral glucose load was studied in 22 patients with cystic fibrosis (CF) by means of insulin, C-peptide an …
Serum antibodies to Aspergillus fumigatus catalase in patients with cystic fibrosis.
Schønheyder H, Jensen T, Laessøe IH, Høiby N, Koch C. Schønheyder H, et al. Among authors: koch c. Eur J Clin Microbiol Infect Dis. 1988 Feb;7(1):40-4. doi: 10.1007/BF01962169. Eur J Clin Microbiol Infect Dis. 1988. PMID: 3132374
Correlation between specific IgG subclass antibodies to Pseudomonas aeruginosa and opsonic activity in serum from patients with cystic fibrosis.
Pressler T, Jensen ET, Espersen F, Pedersen SS, Høiby N, Koch C. Pressler T, et al. Among authors: koch c. Pediatr Pulmonol. 1994 Jan;17(1):31-40. doi: 10.1002/ppul.1950170107. Pediatr Pulmonol. 1994. PMID: 8108174
Cystic fibrosis; hint of linkage with F13B.
Eiberg H, Schmiegelow K, Koch C, Mohr J, Schwartz M, Niebuhr E. Eiberg H, et al. Among authors: koch c. Clin Genet. 1985 Feb;27(2):206. doi: 10.1111/j.1399-0004.1985.tb00213.x. Clin Genet. 1985. PMID: 3856494 No abstract available.
[Prevention of cystic fibrosis?].
Koch C. Koch C. Ugeskr Laeger. 1996 Aug 12;158(33):4622. Ugeskr Laeger. 1996. PMID: 8760516 Danish. No abstract available.
Glucose tolerance in patients with cystic fibrosis: five year prospective study.
Lanng S, Hansen A, Thorsteinsson B, Nerup J, Koch C. Lanng S, et al. Among authors: koch c. BMJ. 1995 Sep 9;311(7006):655-9. doi: 10.1136/bmj.311.7006.655. BMJ. 1995. PMID: 7549632 Free PMC article.
[Mortality in cystic fibrosis].
Koch C. Koch C. Ugeskr Laeger. 1997 Sep 22;159(39):5779. Ugeskr Laeger. 1997. PMID: 9340880 Danish. No abstract available.
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