-
1
-
-
0002310747
-
Bronchiectasis
-
Murray JF, Nadel JA, eds. Philadelphia: WB Saunders
-
Luce JM. Bronchiectasis. In: Murray JF, Nadel JA, eds. Textbook of Respiratory Medicine. 2nd ed. Philadelphia: WB Saunders; 1994:1398-1417
-
(1994)
Textbook of Respiratory Medicine. 2nd Ed.
, pp. 1398-1417
-
-
Luce, J.M.1
-
2
-
-
0000149569
-
Obstructive diseases
-
Murray JF, Nadel JA, eds. Philadelphia: WB Saunders
-
Nadel JA. Obstructive diseases. In: Murray JF, Nadel JA, eds. Textbook of Respiratory Medicine. 2nd ed. Philadelphia: WB Saunders; 1994:1245-1258
-
(1994)
Textbook of Respiratory Medicine. 2nd Ed.
, pp. 1245-1258
-
-
Nadel, J.A.1
-
3
-
-
0033773862
-
An investigation into causative factors in patients with bronchiectasis
-
Pasteur MC, Helliwell SM, Houghton SJ, et al. An investigation into causative factors in patients with bronchiectasis. Am J Respir Crit Care Med 2000;162:1277-1284
-
(2000)
Am J Respir Crit Care Med
, vol.162
, pp. 1277-1284
-
-
Pasteur, M.C.1
Helliwell, S.M.2
Houghton, S.J.3
-
4
-
-
0032469810
-
Genetics of chronic obstructive pulmonary disease and disseminated bronchiectasis
-
Luisetti M, Gilè SL, Bombieri C, Benetazzo MG, Pignatti PF. Genetics of chronic obstructive pulmonary disease and disseminated bronchiectasis. Monaldi Arch Chest Dis 1998;53:614-616
-
(1998)
Monaldi Arch Chest Dis
, vol.53
, pp. 614-616
-
-
Luisetti, M.1
Gilè, S.L.2
Bombieri, C.3
Benetazzo, M.G.4
Pignatti, P.F.5
-
5
-
-
0025391789
-
The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary disease
-
Gasparini P, Savoia A, Luisetti M, Peona V, Pignatti PF. The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol 1990;2:297-299
-
(1990)
Am J Respir Cell Mol Biol
, vol.2
, pp. 297-299
-
-
Gasparini, P.1
Savoia, A.2
Luisetti, M.3
Peona, V.4
Pignatti, P.F.5
-
6
-
-
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;245:1073-1080
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
-
7
-
-
0025885175
-
Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease
-
Poller W, Faber J-P, Scholz S, Olek K, Müller K-M. Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Klin Wochenschr 1991;69:657-663
-
(1991)
Klin Wochenschr
, vol.69
, pp. 657-663
-
-
Poller, W.1
Faber, J.-P.2
Scholz, S.3
Olek, K.4
Müller, K.-M.5
-
8
-
-
0027360503
-
Sweat chloride and ΔF508 mutation in chronic bronchitis or bronchiectasis
-
Gervais R, Lafitte J-J, Dumur V, et al. Sweat chloride and ΔF508 mutation in chronic bronchitis or bronchiectasis. Lancet 1993;342:997
-
(1993)
Lancet
, vol.342
, pp. 997
-
-
Gervais, R.1
Lafitte, J.-J.2
Dumur, V.3
-
9
-
-
0028958565
-
Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis
-
Pignatti PF, Bombieri C, Marigo C, Benetazzo MG, Luisetti M. Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis. Hum Mol Genet 1995;4:635-639
-
(1995)
Hum Mol Genet
, vol.4
, pp. 635-639
-
-
Pignatti, P.F.1
Bombieri, C.2
Marigo, C.3
Benetazzo, M.G.4
Luisetti, M.5
-
10
-
-
0029960243
-
CFTR gene variant IVS8-5T in disseminated bronchiectasis
-
Pignatti PF, Bombieri C, Benetazzo MG, et al. CFTR gene variant IVS8-5T in disseminated bronchiectasis. Am J Hum Genet 1996;58:889-892
-
(1996)
Am J Hum Genet
, vol.58
, pp. 889-892
-
-
Pignatti, P.F.1
Bombieri, C.2
Benetazzo, M.G.3
-
11
-
-
0032435286
-
Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease
-
Bombieri C, Benetazzo MG, Saccomani A, et al. Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease. Hum Genet 1998;103:718-722
-
(1998)
Hum Genet
, vol.103
, pp. 718-722
-
-
Bombieri, C.1
Benetazzo, M.G.2
Saccomani, A.3
-
12
-
-
12644300645
-
CFTR gene mutations in adults with disseminated bronchiectasis
-
Girodon E, Cazeneuve C, Labargy F, et al. CFTR gene mutations in adults with disseminated bronchiectasis. Eur J Hum Genet 1997;5:149-155
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 149-155
-
-
Girodon, E.1
Cazeneuve, C.2
Labargy, F.3
-
13
-
-
0035070082
-
CFTR gene mutations - Including three novel nucleotide substitutions - And haplotype background in patients with asthma, disseminated bronchiectasis, and chronic obstructive pulmonary disease
-
Tzetis M, Efthymiadou A, Strofalis S, et al. CFTR gene mutations - including three novel nucleotide substitutions - and haplotype background in patients with asthma, disseminated bronchiectasis, and chronic obstructive pulmonary disease. Hum Genet 2001;108:216-221
-
(2001)
Hum Genet
, vol.108
, pp. 216-221
-
-
Tzetis, M.1
Efthymiadou, A.2
Strofalis, S.3
-
14
-
-
0038181743
-
-
Cystic Fibrosis Genetic Analysis Consortium Web site: http://www.genet.sickkids.on.ca/cftr. Accessed March 2002
-
-
-
-
15
-
-
0027502580
-
Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
-
Chu C-S, Trapnell BC, Curristin S, Cutting GR, Crystal RG. Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nat Genet 1993;3:151-156
-
(1993)
Nat Genet
, vol.3
, pp. 151-156
-
-
Chu, C.-S.1
Trapnell, B.C.2
Curristin, S.3
Cutting, G.R.4
Crystal, R.G.5
-
16
-
-
0028086056
-
A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat test chloride concentrations
-
Highsmith WE, Burch LH, Zhou Z, et al. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat test chloride concentrations. N Engl J Med 1994;331:974-980
-
(1994)
N Engl J Med
, vol.331
, pp. 974-980
-
-
Highsmith, W.E.1
Burch, L.H.2
Zhou, Z.3
-
17
-
-
0032518518
-
Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes: The polymorphic (TG)m locus explains the partial penetrance of the 5T polymorphism as a disease mutation
-
Cuppens H, Lin W, Jaspers M, et al. Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes: the polymorphic (TG)m locus explains the partial penetrance of the 5T polymorphism as a disease mutation. J Clin Invest 1998;101:487-496
-
(1998)
J Clin Invest
, vol.101
, pp. 487-496
-
-
Cuppens, H.1
Lin, W.2
Jaspers, M.3
-
18
-
-
0032877043
-
Alpha 1-antitrypsin TAQI polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease
-
Benetazzo MG, Gilè LS, Bombieri C, et al. Alpha 1-antitrypsin TAQI polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease. Respir Med 1999;93:648-654
-
(1999)
Respir Med
, vol.93
, pp. 648-654
-
-
Benetazzo, M.G.1
Gilè, L.S.2
Bombieri, C.3
-
19
-
-
0033995116
-
Distribution of α1-antitrypsin alleles in patients with bronchiectasis
-
Cuvalier A, Muir J-F, Hellot M-F, et al. Distribution of α1-antitrypsin alleles in patients with bronchiectasis. Chest 2000;117:415-419
-
(2000)
Chest
, vol.117
, pp. 415-419
-
-
Cuvalier, A.1
Muir, J.-F.2
Hellot, M.-F.3
-
20
-
-
0034033416
-
Tumor necrosis factor gene complex in COPD and disseminated bronchiectasis
-
Patuzzo C, Gilè LS, Zorzetto M, et al. Tumor necrosis factor gene complex in COPD and disseminated bronchiectasis. Chest 2000;117:1353-1358
-
(2000)
Chest
, vol.117
, pp. 1353-1358
-
-
Patuzzo, C.1
Gilè, L.S.2
Zorzetto, M.3
-
21
-
-
0344242139
-
Increased frequency of cystic fibrosis ΔF508 mutation in bronchiectasis associated with rheumatoid arthritis
-
Puéchal X, Fajac I, Bienvenu T, et al. Increased frequency of cystic fibrosis ΔF508 mutation in bronchiectasis associated with rheumatoid arthritis. Eur Respir J 1999;13:1281-1287
-
(1999)
Eur Respir J
, vol.13
, pp. 1281-1287
-
-
Puéchal, X.1
Fajac, I.2
Bienvenu, T.3
-
22
-
-
0033638696
-
Increased frequency of HLA-DRB1*0401 in patients with RA and bronchiectasis
-
Toussirot E, Despaux J, Wendling D. Increased frequency of HLA-DRB1*0401 in patients with RA and bronchiectasis. Ann Rheum Dis 2000;59:1002-1003
-
(2000)
Ann Rheum Dis
, vol.59
, pp. 1002-1003
-
-
Toussirot, E.1
Despaux, J.2
Wendling, D.3
-
23
-
-
0034109607
-
Genotype and phenotype in cystic fibrosis
-
Zielenski J. Genotype and phenotype in cystic fibrosis. Respiration 2000;67:117-133
-
(2000)
Respiration
, vol.67
, pp. 117-133
-
-
Zielenski, J.1
-
24
-
-
0029896266
-
Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis
-
Weiner Miller P, Hamosh A, Macek M Jr, et al. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis. Am J Hum Genet 1996;59:45-51
-
(1996)
Am J Hum Genet
, vol.59
, pp. 45-51
-
-
Weiner Miller, P.1
Hamosh, A.2
Macek M., Jr.3
-
25
-
-
0030919876
-
Genetic risk factors for chronic obstructive pulmonary disease
-
Sandford AJ, Weir TD, Paré PD. Genetic risk factors for chronic obstructive pulmonary disease. Eur Respir J 1997;10:1380-1391
-
(1997)
Eur Respir J
, vol.10
, pp. 1380-1391
-
-
Sandford, A.J.1
Weir, T.D.2
Paré, P.D.3
-
26
-
-
0033093103
-
Molecular genetics of chronic obstructive pulmonary disease
-
Barnes PJ. Molecular genetics of chronic obstructive pulmonary disease. Thorax 1999;54:245-252
-
(1999)
Thorax
, vol.54
, pp. 245-252
-
-
Barnes, P.J.1
-
27
-
-
0027462536
-
Management of chronic obstructive pulmonary disease
-
Ferguson GT, Cherniack RM. Management of chronic obstructive pulmonary disease. N Engl J Med 1993;328:1017-1022
-
(1993)
N Engl J Med
, vol.328
, pp. 1017-1022
-
-
Ferguson, G.T.1
Cherniack, R.M.2
-
28
-
-
0033925717
-
Physiological and radiological characterisation of patients diagnosed with chronic obstructive pulmonary disease in primary care
-
O'Brien C, Guest PJ, Hill SL, Stockley RA. Physiological and radiological characterisation of patients diagnosed with chronic obstructive pulmonary disease in primary care. Thorax 2000;55:635-642
-
(2000)
Thorax
, vol.55
, pp. 635-642
-
-
O'Brien, C.1
Guest, P.J.2
Hill, S.L.3
Stockley, R.A.4
-
29
-
-
0033910486
-
The heterogeneity of chronic obstructive pulmonary disease
-
Wedzicha JA. The heterogeneity of chronic obstructive pulmonary disease. Thorax 2000;55:631-632
-
(2000)
Thorax
, vol.55
, pp. 631-632
-
-
Wedzicha, J.A.1
-
30
-
-
0029616734
-
Cystic fibrosis: Genotypic and phenotypic variations
-
Zielenski J, Tsui LC. Cystic fibrosis: genotypic and phenotypic variations. Annu Rev Genet 1995;29:777-807
-
(1995)
Annu Rev Genet
, vol.29
, pp. 777-807
-
-
Zielenski, J.1
Tsui, L.C.2
-
31
-
-
0024988766
-
Abnormal distribution of the CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens [Letter]
-
Dumur V, Gervais R, Rigot JM, et al. Abnormal distribution of the CF delta F508 allele in azoospermic men with congenital aplasia of epididymis and vas deferens [Letter]. Lancet 1990;336:512
-
(1990)
Lancet
, vol.336
, pp. 512
-
-
Dumur, V.1
Gervais, R.2
Rigot, J.M.3
-
32
-
-
0033724681
-
Lung disease associated with the IVS8 5T allele of the CFTR gene
-
Noone PG, Pue CA, Zhou Z, et al. Lung disease associated with the IVS8 5T allele of the CFTR gene. Am J Respir Crit Care Med 2000;162:1919-1924
-
(2000)
Am J Respir Crit Care Med
, vol.162
, pp. 1919-1924
-
-
Noone, P.G.1
Pue, C.A.2
Zhou, Z.3
-
33
-
-
0038181738
-
Unique presentations and chronic complications in adult cystic fibrosis: Do they teach anything about CFTR?
-
Boyle MP. Unique presentations and chronic complications in adult cystic fibrosis: do they teach anything about CFTR? Respir Res 2000;1:133-135
-
(2000)
Respir Res
, vol.1
, pp. 133-135
-
-
Boyle, M.P.1
-
34
-
-
0035722764
-
"CFTR-opathies": Disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations
-
Noone PG, Knowles MR. "CFTR-opathies": disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations. Respir Res 2001;2:328-332
-
(2001)
Respir Res
, vol.2
, pp. 328-332
-
-
Noone, P.G.1
Knowles, M.R.2
-
35
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillon M, Casals T, Mercier B, et al. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N Engl J Med 1995;332:1475-1480
-
(1995)
N Engl J Med
, vol.332
, pp. 1475-1480
-
-
Chillon, M.1
Casals, T.2
Mercier, B.3
-
36
-
-
0029151485
-
CFTR gene variant for patients with congenital absence of vas deferens
-
Zielenski J, Patrizio P, Corey M, et al. CFTR gene variant for patients with congenital absence of vas deferens. Am J Hum Genet 1995;57:958-960
-
(1995)
Am J Hum Genet
, vol.57
, pp. 958-960
-
-
Zielenski, J.1
Patrizio, P.2
Corey, M.3
|