-
1
-
-
0037406739
-
Haemochromatosis
-
Suppl.
-
Pietrangelo A. Haemochromatosis. Gut 2003 52 (Suppl. 2 ii23 30.
-
(2003)
Gut
, vol.52
, Issue.2
, pp. 23-30
-
-
Pietrangelo, A.1
-
2
-
-
0035737072
-
Phenotype of CF and the effects of possible modifier genes
-
Acton JD, Wilmott RW. Phenotype of CF and the effects of possible modifier genes. Paediatr. Respir. Rev. 2001 2 : 332 339.
-
(2001)
Paediatr. Respir. Rev.
, vol.2
, pp. 332-339
-
-
Acton, J.D.1
Wilmott, R.W.2
-
5
-
-
33750454431
-
Disease modifying genes in cystic fibrosis: Therapeutic option or one-way road?
-
Buscher R, Grasemann H. Disease modifying genes in cystic fibrosis: therapeutic option or one-way road? Naunyn Schmiedebergs Arch. Pharmacol. 2006 374 : 65 77.
-
(2006)
Naunyn Schmiedebergs Arch. Pharmacol.
, vol.374
, pp. 65-77
-
-
Buscher, R.1
Grasemann, H.2
-
6
-
-
0037388124
-
Modifier genes in cystic fibrosis lung disease
-
Merlo CA, Boyle MP. Modifier genes in cystic fibrosis lung disease. J. Lab. Clin. Med. 2003 141 : 237 241.
-
(2003)
J. Lab. Clin. Med.
, vol.141
, pp. 237-241
-
-
Merlo, C.A.1
Boyle, M.P.2
-
7
-
-
33750954504
-
Polymorphisms of TGF-beta1 in cystic fibrosis patients
-
Brazova J, Sismova K, Vavrova V et al. Polymorphisms of TGF-beta1 in cystic fibrosis patients. Clin. Immunol. 2006 121 : 350 357.
-
(2006)
Clin. Immunol.
, vol.121
, pp. 350-357
-
-
Brazova, J.1
Sismova, K.2
Vavrova, V.3
-
8
-
-
34147103990
-
Variants in mannose-binding lectin and tumor necrosis factor {alpha} affect survival in cystic fibrosis
-
Buranawuti K, Boyle MP, Cheng S et al. Variants in mannose-binding lectin and tumor necrosis factor {alpha} affect survival in cystic fibrosis. J. Med. Genet. 2007 44 : 209 214.
-
(2007)
J. Med. Genet.
, vol.44
, pp. 209-214
-
-
Buranawuti, K.1
Boyle, M.P.2
Cheng, S.3
-
9
-
-
13544273186
-
Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: Bacterial colonization may be decisive for a relationship
-
Carlsson M, Sjoholm AG, Eriksson L et al. Deficiency of the mannan-binding lectin pathway of complement and poor outcome in cystic fibrosis: bacterial colonization may be decisive for a relationship. Clin. Exp. Immunol. 2005 139 : 306 313.
-
(2005)
Clin. Exp. Immunol.
, vol.139
, pp. 306-313
-
-
Carlsson, M.1
Sjoholm, A.G.2
Eriksson, L.3
-
10
-
-
8644255090
-
Impaired pulmonary status in cystic fibrosis adults with two mutated MBL-2 alleles
-
Davies JC, Turner MW, Klein N. Impaired pulmonary status in cystic fibrosis adults with two mutated MBL-2 alleles. Eur. Respir. J. 2004 24 : 798 804.
-
(2004)
Eur. Respir. J.
, vol.24
, pp. 798-804
-
-
Davies, J.C.1
Turner, M.W.2
Klein, N.3
-
11
-
-
0037477694
-
HFE alleles in an Irish cystic fibrosis population
-
DOI 10.1089/109065703322146876
-
Devaney J, Maher M, Smith T et al. HFE alleles in an Irish cystic fibrosis population. Genet. Test. 2003 7 : 155 158. (Pubitemid 36842207)
-
(2003)
Genetic Testing
, vol.7
, Issue.2
, pp. 155-158
-
-
Devaney, J.1
Maher, M.2
Smith, T.3
Houghton, J.A.4
Glennon, M.5
-
12
-
-
0032250506
-
Is the hemochromatosis gene a modifier locus for cystic fibrosis?
-
Rohlfs EM, Shaheen NJ, Silverman LM. Is the hemochromatosis gene a modifier locus for cystic fibrosis? Genet. Test. 1998 2 : 85 8.
-
(1998)
Genet. Test.
, vol.2
, pp. 85-8
-
-
Rohlfs, E.M.1
Shaheen, N.J.2
Silverman, L.M.3
-
13
-
-
34547590582
-
Increased airway iron as a potential factor in the persistence of Pseudomonas aeruginosa infection in cystic fibrosis
-
Reid DW, Carroll V, O'May C et al. Increased airway iron as a potential factor in the persistence of Pseudomonas aeruginosa infection in cystic fibrosis. Eur. Respir. J. 2007 30 : 286 292.
-
(2007)
Eur. Respir. J.
, vol.30
, pp. 286-292
-
-
Reid, D.W.1
Carroll, V.2
O'May, C.3
-
14
-
-
4344675647
-
Airway iron and iron-regulatory cytokines in cystic fibrosis
-
Reid DW, Lam QT, Schneider H et al. Airway iron and iron-regulatory cytokines in cystic fibrosis. Eur. Respir. J. 2004 24 : 286 291.
-
(2004)
Eur. Respir. J.
, vol.24
, pp. 286-291
-
-
Reid, D.W.1
Lam, Q.T.2
Schneider, H.3
-
15
-
-
0036152945
-
Iron deficiency in cystic fibrosis: Relationship to lung disease severity and chronic Pseudomonas aeruginosa infection
-
Reid DW, Withers NJ, Francis L et al. Iron deficiency in cystic fibrosis: relationship to lung disease severity and chronic Pseudomonas aeruginosa infection. Chest 2002 121 : 48 54.
-
(2002)
Chest
, vol.121
, pp. 48-54
-
-
Reid, D.W.1
Withers, N.J.2
Francis, L.3
-
16
-
-
0032827424
-
Increased concentrations of iron and isoferritins in the lower respiratory tract of patients with stable cystic fibrosis
-
Stites SW, Plautz MW, Bailey K et al. Increased concentrations of iron and isoferritins in the lower respiratory tract of patients with stable cystic fibrosis. Am. J. Respir. Crit. Care Med. 1999 160 : 796 801.
-
(1999)
Am. J. Respir. Crit. Care Med.
, vol.160
, pp. 796-801
-
-
Stites, S.W.1
Plautz, M.W.2
Bailey, K.3
-
17
-
-
49049089612
-
The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability
-
37.
-
Moreau-Marquis S, Bomberger JM, Anderson GG et al. The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability. Am. J. Physiol. Lung Cell Mol. Physiol. 2008 295 : L25 37.
-
(2008)
Am. J. Physiol. Lung Cell Mol. Physiol.
, vol.295
, pp. 25
-
-
Moreau-Marquis, S.1
Bomberger, J.M.2
Anderson, G.G.3
-
19
-
-
0037298439
-
A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population
-
Malecki MT, Klupa T, Walus M et al. A search for association between hereditary hemochromatosis HFE gene mutations and type 2 diabetes mellitus in a Polish population. Med. Sci. Monit. 2003 9 : BR91 95.
-
(2003)
Med. Sci. Monit.
, vol.9
, pp. 91-95
-
-
Malecki, M.T.1
Klupa, T.2
Walus, M.3
-
20
-
-
34248583747
-
Importance of hereditary haemochromatosis in the care of diabetes mellitus
-
Wittmann I, Wagner L, Marko L et al. Importance of hereditary haemochromatosis in the care of diabetes mellitus Orv. Hetil. 2007 148 : 111 115.
-
(2007)
Orv. Hetil.
, vol.148
, pp. 111-115
-
-
Wittmann, I.1
Wagner, L.2
Marko, L.3
-
21
-
-
0346158239
-
A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes
-
DOI 10.1007/s10038-003-0094-3
-
Peterlin B, Globocnik Petrovic M, Makuc J et al. A hemochromatosis- causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes. J. Hum. Genet. 2003 48 : 646 649. (Pubitemid 38031308)
-
(2003)
Journal of Human Genetics
, vol.48
, Issue.12
, pp. 646-649
-
-
Peterlin, B.1
Petrovic, M.G.2
Makuc, J.3
Hawlina, M.4
Petrovic, D.5
-
22
-
-
0035403064
-
Role of hemochromatosis C282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy
-
Moczulski DK, Grzeszczak W, Gawlik B. Role of hemochromatosis C282Y and H63D mutations in HFE gene in development of type 2 diabetes and diabetic nephropathy. Diabetes Care 2001 24 : 1187 1191.
-
(2001)
Diabetes Care
, vol.24
, pp. 1187-1191
-
-
Moczulski, D.K.1
Grzeszczak, W.2
Gawlik, B.3
-
23
-
-
0037252230
-
Factors influencing outcomes in cystic fibrosis: A center-based analysis
-
Johnson C, Butler SM, Konstan MW et al. Factors influencing outcomes in cystic fibrosis: a center-based analysis. Chest 2003 123 : 20 7.
-
(2003)
Chest
, vol.123
, pp. 20-7
-
-
Johnson, C.1
Butler, S.M.2
Konstan, M.W.3
-
24
-
-
0036163928
-
Case-mix adjustment for evaluation of mortality in cystic fibrosis
-
O'Connor GT, Quinton HB, Kahn R et al. Case-mix adjustment for evaluation of mortality in cystic fibrosis. Pediatr. Pulmonol. 2002 33 : 99 105.
-
(2002)
Pediatr. Pulmonol.
, vol.33
, pp. 99-105
-
-
O'Connor, G.T.1
Quinton, H.B.2
Kahn, R.3
-
25
-
-
17244382014
-
New criteria for impaired fasting glucose and screening for diabetes in cystic fibrosis
-
Mueller-Brandes C, Holl RW, Nastoll M et al. New criteria for impaired fasting glucose and screening for diabetes in cystic fibrosis. Eur. Respir. J. 2005 25 : 715 717.
-
(2005)
Eur. Respir. J.
, vol.25
, pp. 715-717
-
-
Mueller-Brandes, C.1
Holl, R.W.2
Nastoll, M.3
-
26
-
-
33846920612
-
The use of soluble transferrin receptor to assess iron deficiency in adults with cystic fibrosis
-
Khalid S, McGrowder D, Kemp M et al. The use of soluble transferrin receptor to assess iron deficiency in adults with cystic fibrosis. Clin. Chim. Acta 2007 378 : 194 200.
-
(2007)
Clin. Chim. Acta
, vol.378
, pp. 194-200
-
-
Khalid, S.1
McGrowder, D.2
Kemp, M.3
-
27
-
-
0034976902
-
Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis
-
Lucotte G. Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis. Blood Cells Mol. Dis. 2001 27 : 549 556.
-
(2001)
Blood Cells Mol. Dis.
, vol.27
, pp. 549-556
-
-
Lucotte, G.1
-
28
-
-
0033862923
-
Celtic origin of the C282Y mutation of hemochromatosis
-
Lucotte G, Mercier G. Celtic origin of the C282Y mutation of hemochromatosis. Genet. Test. 2000 4 : 163 169.
-
(2000)
Genet. Test.
, vol.4
, pp. 163-169
-
-
Lucotte, G.1
Mercier, G.2
-
30
-
-
38349079861
-
Iron-overload-related disease in HFE hereditary hemochromatosis
-
Allen KJ, Gurrin LC, Constantine CC et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N. Engl. J. Med. 2008 358 : 221 230.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 221-230
-
-
Allen, K.J.1
Gurrin, L.C.2
Constantine, C.C.3
-
31
-
-
0002865686
-
Cystic fibrosis-related diabetes: An approach to diagnosis and management
-
Moran A. Cystic fibrosis-related diabetes: an approach to diagnosis and management. Pediatr. Diabetes 2000 1 : 41 8.
-
(2000)
Pediatr. Diabetes
, vol.1
, pp. 41-8
-
-
Moran, A.1
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