-
1
-
-
0031053826
-
Geographical differences in prevalence of hepatitis C virus infection in PCT
-
Malina M, Stransky J, Zdarsky E: Geographical differences in prevalence of hepatitis C virus infection in PCT. Br J Dermatol 1997; 136:291-292.
-
(1997)
Br J Dermatol
, vol.136
, pp. 291-292
-
-
Malina, M.1
Stransky, J.2
Zdarsky, E.3
-
3
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, Tsuchiashi Z, Ruddy DA, Basava A: A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 1996;13:399-408.
-
(1996)
Nat Genet
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
Tsuchiashi, Z.4
Ruddy, D.A.5
Basava, A.6
-
4
-
-
0033561342
-
HFE mutation analysis in 711 hemochromatosis probands: Evidence for S65C implication in a mild form of hemochromatosis
-
Mura C, Raguenes O, Férec C: HFE mutation analysis in 711 hemochromatosis probands: Evidence for S65C implication in a mild form of hemochromatosis. Blood 1999;93:2502-2505.
-
(1999)
Blood
, vol.93
, pp. 2502-2505
-
-
Mura, C.1
Raguenes, O.2
Férec, C.3
-
5
-
-
13144282684
-
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
-
Feder JN, Penny DM, Irrinki A, Lee V, Lebron J, Watson N, Tsuchihashi Z, Sigal E, Bjorkman P, Schatzman R: The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proc Natl Acad Sci USA 1998;95:1472-1477.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 1472-1477
-
-
Feder, J.N.1
Penny, D.M.2
Irrinki, A.3
Lee, V.4
Lebron, J.5
Watson, N.6
Tsuchihashi, Z.7
Sigal, E.8
Bjorkman, P.9
Schatzman, R.10
-
6
-
-
0037117603
-
Iron uptake from plasma transferrin by the duodenum is impaired in the HFE knockout mouse
-
Trinder D, Olynyk JK, Sly WS, Morgan EH: Iron uptake from plasma transferrin by the duodenum is impaired in the HFE knockout mouse. Proc Natl Acad Sci 2002;99:5622-5626.
-
(2002)
Proc Natl Acad Sci
, vol.99
, pp. 5622-5626
-
-
Trinder, D.1
Olynyk, J.K.2
Sly, W.S.3
Morgan, E.H.4
-
7
-
-
85033510543
-
Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload
-
Elder GH, Worwood M: Mutations in the hemochromatosis gene, porphyria cutanea tarda, and iron overload. Hepatology 1998;27:181.
-
(1998)
Hepatology
, vol.27
, pp. 181
-
-
Elder, G.H.1
Worwood, M.2
-
8
-
-
0031022078
-
The frequency of haemochromatosis associated alleles is increased in British patients with sporadic porphyria cutanea tarda
-
Roberts AG, Whatley SD, Nicklin S, Worwood M, Pointon J, Stone C, Elder G: The frequency of haemochromatosis associated alleles is increased in British patients with sporadic porphyria cutanea tarda. Hepatology 1997;25: 159-161.
-
(1997)
Hepatology
, vol.25
, pp. 159-161
-
-
Roberts, A.G.1
Whatley, S.D.2
Nicklin, S.3
Worwood, M.4
Pointon, J.5
Stone, C.6
Elder, G.7
-
9
-
-
0031016791
-
Increase frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
-
Roberts A, Whatley S, Morgan R, Worwood M, Elder G: Increase frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda. Lancet 1997;349:321-323.
-
(1997)
Lancet
, vol.349
, pp. 321-323
-
-
Roberts, A.1
Whatley, S.2
Morgan, R.3
Worwood, M.4
Elder, G.5
-
10
-
-
0032030738
-
The C282Y mutation in the haemochromatosis gene and hepatitis virus infection are independent cofactors for porphyria cutanea tarda in Australian patients
-
Stuart KA, Busfield F, Jazwinska EC, Gibson P, Butterworth L, Cooksley WG, Powell L, Crawford D: The C282Y mutation in the haemochromatosis gene and hepatitis virus infection are independent cofactors for porphyria cutanea tarda in Australian patients. J Hepatol 1998;28:404-409.
-
(1998)
J Hepatol
, vol.28
, pp. 404-409
-
-
Stuart, K.A.1
Busfield, F.2
Jazwinska, E.C.3
Gibson, P.4
Butterworth, L.5
Cooksley, W.G.6
Powell, L.7
Crawford, D.8
-
11
-
-
0033638582
-
Porphyria cutanea tarda in Brazilian patients: Association with hemochromatosis C282Y mutation and hepatitis C virus infection
-
Martinelli AL, Zago MA, Roselino AM, Filho AB, Villanova MG, Secaf M, Tavella MH, Ramalho LN, Zucoloto S, Franco RF: Porphyria cutanea tarda in Brazilian patients: Association with hemochromatosis C282Y mutation and hepatitis C virus infection. Am J Gastroenterol 2000;95:3516-3521.
-
(2000)
Am J Gastroenterol
, vol.95
, pp. 3516-3521
-
-
Martinelli, A.L.1
Zago, M.A.2
Roselino, A.M.3
Filho, A.B.4
Villanova, M.G.5
Secaf, M.6
Tavella, M.H.7
Ramalho, L.N.8
Zucoloto, S.9
Franco, R.F.10
-
12
-
-
0031982781
-
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda
-
Sampietro M, Piperno A, Lupica L, Arosio C, Vergani A, Corbetta N, Malosio I, Mattioli M, Fracanzani AL, Cappellini D, Fiorelli G, Fargion S: High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda. Hepatology 1998;27:181-184.
-
(1998)
Hepatology
, vol.27
, pp. 181-184
-
-
Sampietro, M.1
Piperno, A.2
Lupica, L.3
Arosio, C.4
Vergani, A.5
Corbetta, N.6
Malosio, I.7
Mattioli, M.8
Fracanzani, A.L.9
Cappellini, D.10
Fiorelli, G.11
Fargion, S.12
-
13
-
-
0032858374
-
The most frequent HFE allele linked to porphyria cutanea tarda in Mediterraneans is Hi63Asp
-
Enriquez de Salamanca R, Morales P, Castro M, Rojo R, Gonzalez M, Arnaiz-Villena A: The most frequent HFE allele linked to porphyria cutanea tarda in Mediterraneans is Hi63Asp. Hepatology 1999;30:819-820.
-
(1999)
Hepatology
, vol.30
, pp. 819-820
-
-
Enriquez de Salamanca, R.1
Morales, P.2
Castro, M.3
Rojo, R.4
Gonzalez, M.5
Arnaiz-Villena, A.6
-
14
-
-
0029903136
-
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: Possible explanation for iron overload
-
Fargion S, Fracanzani AL, Romano R, Cappellini M, Faré M, Mattioli M, Piperno A, Ronchi G, Fiorelli G: Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: Possible explanation for iron overload. J Hepatol 1996;24:564-569.
-
(1996)
J Hepatol
, vol.24
, pp. 564-569
-
-
Fargion, S.1
Fracanzani, A.L.2
Romano, R.3
Cappellini, M.4
Faré, M.5
Mattioli, M.6
Piperno, A.7
Ronchi, G.8
Fiorelli, G.9
-
15
-
-
85048354015
-
Are His63Asp or Cys282Tyr HFE mutations associated with porphyria cutanea tarda? Data of patients from central and southern Italy
-
D'Amato M, Macri A, Griso D, Biolcati G, Ameglio F: Are His63Asp or Cys282Tyr HFE mutations associated with porphyria cutanea tarda? Data of patients from central and southern Italy. J Invest Dermatol 1998;111:1242-1243.
-
(1998)
J Invest Dermatol
, vol.111
, pp. 1242-1243
-
-
D'Amato, M.1
Macri, A.2
Griso, D.3
Biolcati, G.4
Ameglio, F.5
-
16
-
-
0035087466
-
HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: A prospective study of 36 cases from southern France
-
Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou JJ: HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: A prospective study of 36 cases from southern France. Br J Dermatol 2001;14:533-539.
-
(2001)
Br J Dermatol
, vol.14
, pp. 533-539
-
-
Dereure, O.1
Aguilar-Martinez, P.2
Bessis, D.3
Perney, P.4
Vallat, C.5
Guillot, B.6
Blanc, F.7
Guilhou, J.J.8
-
17
-
-
0027458392
-
Porphyria cutanea tarda and antibodies to hepatitis C virus
-
Lacour JPH, Bodokh I, Castanet J: Porphyria cutanea tarda and antibodies to hepatitis C virus. Br J Dermatol 1993;128:121-123.
-
(1993)
Br J Dermatol
, vol.128
, pp. 121-123
-
-
Lacour, J.P.H.1
Bodokh, I.2
Castanet, J.3
-
18
-
-
0031891753
-
Hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda patients: The influence of virus C infection
-
Moran MJ, Fontanellas A, Brudieux E, Hombrados I, De Ledingjen V, Couzigou P, De Verneuil H, Enriquez de Salamanca R: Hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda patients: The influence of virus C infection. Hepatology 1998; 27:584-589.
-
(1998)
Hepatology
, vol.27
, pp. 584-589
-
-
Moran, M.J.1
Fontanellas, A.2
Brudieux, E.3
Hombrados, I.4
De Ledingjen, V.5
Couzigou, P.6
De Verneuil, H.7
Enriquez de Salamanca, R.8
-
19
-
-
0032793401
-
Porphyria cutanea tarda and hepatitis C virus: A case control study and meta-analysis of the literature
-
Chuang T, Brashear R, Lewis C: Porphyria cutanea tarda and hepatitis C virus: A case control study and meta-analysis of the literature. J Am Acad Dermatol 1999;41:31-36.
-
(1999)
J Am Acad Dermatol
, vol.41
, pp. 31-36
-
-
Chuang, T.1
Brashear, R.2
Lewis, C.3
-
20
-
-
0032947967
-
The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C
-
Kazemi-Shirazi L, Datz C, Maier-Dobersberger T, Kaserer K, Hackl F, Polli C, Steindl P, Penner E, Ferenci P: The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C. Gastroenterology 1999;116:127-134.
-
(1999)
Gastroenterology
, vol.116
, pp. 127-134
-
-
Kazemi-Shirazi, L.1
Datz, C.2
Maier-Dobersberger, T.3
Kaserer, K.4
Hackl, F.5
Polli, C.6
Steindl, P.7
Penner, E.8
Ferenci, P.9
-
21
-
-
0031891521
-
Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda
-
Lamoril J, Andant C, Bogard C, Puy H, Gouya L, Pawlotsky JM, Da Silva V, Soulé JC, Deybach JC, Nordmann Y: Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda. Hepatology 1998;27:848-852.
-
(1998)
Hepatology
, vol.27
, pp. 848-852
-
-
Lamoril, J.1
Andant, C.2
Bogard, C.3
Puy, H.4
Gouya, L.5
Pawlotsky, J.M.6
Da Silva, V.7
Soulé, J.C.8
Deybach, J.C.9
Nordmann, Y.10
-
22
-
-
0031409432
-
High prevalence of hepatitis C virus type 1b in Italian patients with porphyria cutanea tarda
-
Sampietro M, Fracanzani AL, Corbetta N: High prevalence of hepatitis C virus type 1b in Italian patients with porphyria cutanea tarda. Ital J Gastroenterol Hepatol 1997;29:543-547.
-
(1997)
Ital J Gastroenterol Hepatol
, vol.29
, pp. 543-547
-
-
Sampietro, M.1
Fracanzani, A.L.2
Corbetta, N.3
-
23
-
-
0034609577
-
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic
-
Beutler E, Felitti V, Gelbart T, Ho N: The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Ann Intern Med 2000;133: 329-337.
-
(2000)
Ann Intern Med
, vol.133
, pp. 329-337
-
-
Beutler, E.1
Felitti, V.2
Gelbart, T.3
Ho, N.4
-
24
-
-
17344362638
-
Porphyria cutanea tarda, hepatitis C, and HFE mutations in North America
-
Bonkovsky HL, Poh-Fitzpatrick M, Pimstone N, Obando J, Di Bisceglie A, Tattrie C, Tortorelli K, LeClair P, Mercurio M, Lambrecht R: Porphyria cutanea tarda, hepatitis C, and HFE mutations in North America. Hepatology 1998;27:1661-1669.
-
(1998)
Hepatology
, vol.27
, pp. 1661-1669
-
-
Bonkovsky, H.L.1
Poh-Fitzpatrick, M.2
Pimstone, N.3
Obando, J.4
Di Bisceglie, A.5
Tattrie, C.6
Tortorelli, K.7
LeClair, P.8
Mercurio, M.9
Lambrecht, R.10
-
25
-
-
0034634505
-
Interaction of the ectodomain of HFE with the transferring receptor are critical for iron homeostasis in cells
-
Roy C, Carlson E, Anderson E, Basava A, Starnes S, Feder J, Enns C: Interaction of the ectodomain of HFE with the transferring receptor are critical for iron homeostasis in cells. FEBS Lett 2000;484; 271-274.
-
(2000)
FEBS Lett
, vol.484
, pp. 271-274
-
-
Roy, C.1
Carlson, E.2
Anderson, E.3
Basava, A.4
Starnes, S.5
Feder, J.6
Enns, C.7
-
26
-
-
0034022636
-
The gene TRF2 is mutated in a new type of haemochromatosis mapping to 7q22
-
Camaschella C, Roetto A, Cali A, De Gobbi M, Garozzo G, Carella M, Majorano N, Totaro A, Gasparini P: The gene TRF2 is mutated in a new type of haemochromatosis mapping to 7q22. Nat Genet 2000;25:14-15.
-
(2000)
Nat Genet
, vol.25
, pp. 14-15
-
-
Camaschella, C.1
Roetto, A.2
Cali, A.3
De Gobbi, M.4
Garozzo, G.5
Carella, M.6
Majorano, N.7
Totaro, A.8
Gasparini, P.9
-
27
-
-
17944380796
-
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene
-
Montosi G, Donovan A, Totaro A, Garuti C, Pignatti E, Cassanelli S, Trenor CC, Gasparini P, Andrews NC, Pietrangelo A: Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. J Clin Invest 2001;108:619-623.
-
(2001)
J Clin Invest
, vol.108
, pp. 619-623
-
-
Montosi, G.1
Donovan, A.2
Totaro, A.3
Garuti, C.4
Pignatti, E.5
Cassanelli, S.6
Trenor, C.C.7
Gasparini, P.8
Andrews, N.C.9
Pietrangelo, A.10
-
28
-
-
0036213785
-
No evidence of Y250X transferrin receptor type 2 mutation in patients with porphyria cutanea tarda: A study of 38 cases
-
Dereure O, Esculier C, Aguilar-Martinez P, Dessis D, Guillot B, Guilhou JJ: No evidence of Y250X transferrin receptor type 2 mutation in patients with porphyria cutanea tarda: A study of 38 cases. Dermatology 2002;204:158-159.
-
(2002)
Dermatology
, vol.204
, pp. 158-159
-
-
Dereure, O.1
Esculier, C.2
Aguilar-Martinez, P.3
Dessis, D.4
Guillot, B.5
Guilhou, J.J.6
-
29
-
-
0034999045
-
Variable phenotypic presentation of iron overload in H63D homozygotes: Are genetic modifiers the cause?
-
Martinez PA, Bismuth M, Picot MC, Thelcide C, Pageaux GP, Blanc F, Blanc P, Sched JF, Larrey D: Variable phenotypic presentation of iron overload in H63D homozygotes: Are genetic modifiers the cause? Gut 2001;48:836-842.
-
(2001)
Gut
, vol.48
, pp. 836-842
-
-
Martinez, P.A.1
Bismuth, M.2
Picot, M.C.3
Thelcide, C.4
Pageaux, G.P.5
Blanc, F.6
Blanc, P.7
Sched, J.F.8
Larrey, D.9
-
30
-
-
0037006654
-
Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease and secondary iron overload
-
Townsend A, Drakesmith H: Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease and secondary iron overload. Lancet 2002:359:786-790.
-
(2002)
Lancet
, vol.359
, pp. 786-790
-
-
Townsend, A.1
Drakesmith, H.2
|