-
1
-
-
0032697718
-
Hereditary hemochromatosis: Impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease
-
Press RD. Hereditary hemochromatosis: impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease. Arch Pathol Lab Med 1999;123:1053-1059.
-
(1999)
Arch Pathol Lab Med
, vol.123
, pp. 1053-1059
-
-
Press, R.D.1
-
2
-
-
0032401683
-
Hemochromatosis-associated mortality in the United States from 1979 to 1992: An analysis of multiple-cause mortality data
-
Yang Q, McDonnell SM, Khoury MJ, Cono J, Parrish RG. Hemochromatosis-associated mortality in the United States from 1979 to 1992: an analysis of Multiple-Cause Mortality Data. Ann Intern Med 1998;129:946-953.
-
(1998)
Ann Intern Med
, vol.129
, pp. 946-953
-
-
Yang, Q.1
McDonnell, S.M.2
Khoury, M.J.3
Cono, J.4
Parrish, R.G.5
-
3
-
-
0022368621
-
Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis
-
Niederau C, Fischer R, Sonnenberg A, Stremmel W, Trampisch HJ. Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis. N Engl J Med 1985;313:1256-1262.
-
(1985)
N Engl J Med
, vol.313
, pp. 1256-1262
-
-
Niederau, C.1
Fischer, R.2
Sonnenberg, A.3
Stremmel, W.4
Trampisch, H.J.5
-
4
-
-
0025913745
-
Long-term survival analysis in hereditary hemochromatosis
-
Adams PC, Speechley M, Kertesz AE. Long-term survival analysis in hereditary hemochromatosis. Gastroenterology 1991;101:368-372.
-
(1991)
Gastroenterology
, vol.101
, pp. 368-372
-
-
Adams, P.C.1
Speechley, M.2
Kertesz, A.E.3
-
5
-
-
0029913626
-
Long-term survival in patients with hereditary hemochromatosis
-
Niederau C, Fischer R, Purschel A, Stremmel W, Haussinger D. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology 1996;110:1107-1119.
-
(1996)
Gastroenterology
, vol.110
, pp. 1107-1119
-
-
Niederau, C.1
Fischer, R.2
Purschel, A.3
Stremmel, W.4
Haussinger, D.5
-
6
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Domingo R, et al. 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
Tsuchihashi, Z.4
Ruddy, D.A.5
Basava, A.6
Domingo, R.7
-
7
-
-
0032478524
-
Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor
-
Lebron JA, Bennett MJ, Vaughn DE, Chirino AJ, Snow PM, Mintier GA, Bjorkman PJ. Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor. Cell 1998;93: 111-123.
-
(1998)
Cell
, vol.93
, pp. 111-123
-
-
Lebron, J.A.1
Bennett, M.J.2
Vaughn, D.E.3
Chirino, A.J.4
Snow, P.M.5
Mintier, G.A.6
Bjorkman, P.J.7
-
8
-
-
13144282684
-
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding
-
Feder JN, Penny DM, Irrinki A, Lee VK, Lebron JA, Watson N, Sigal E, et al. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. Proc Natl Acad Sci U S A 1998;95:1472-1477.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 1472-1477
-
-
Feder, J.N.1
Penny, D.M.2
Irrinki, A.3
Lee, V.K.4
Lebron, J.A.5
Watson, N.6
Sigal, E.7
-
9
-
-
0033517343
-
A population-based study of the clinical expression of the hemochromatosis gene
-
Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med 1999;341:718-724.
-
(1999)
N Engl J Med
, vol.341
, pp. 718-724
-
-
Olynyk, J.K.1
Cullen, D.J.2
Aquilia, S.3
Rossi, E.4
Summerville, L.5
Powell, L.W.6
-
10
-
-
0001376313
-
HFE gene knockout produces mouse model of hereditary hemochromatosis
-
Zhou XY, Tomatsu S, Fleming RE, Parkkila S, Waheed A, Jiang J, Fei Y, et al. HFE gene knockout produces mouse model of hereditary hemochromatosis. Proc Natl Acad Sci U S A 1998;95:2492-2497.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 2492-2497
-
-
Zhou, X.Y.1
Tomatsu, S.2
Fleming, R.E.3
Parkkila, S.4
Waheed, A.5
Jiang, J.6
Fei, Y.7
-
11
-
-
0031969395
-
Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation
-
Crawford DH, Jazwinska EC, Cullen LM, Powell LW. Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation. Gastroenterology 1998;114:1003-1008.
-
(1998)
Gastroenterology
, vol.114
, pp. 1003-1008
-
-
Crawford, D.H.1
Jazwinska, E.C.2
Cullen, L.M.3
Powell, L.W.4
-
12
-
-
0032775931
-
Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis
-
Jeffrey GP, Chakrabarti S, Hegele RA, Adams PC. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis. Nat Genet 1999;22:325-326.
-
(1999)
Nat Genet
, vol.22
, pp. 325-326
-
-
Jeffrey, G.P.1
Chakrabarti, S.2
Hegele, R.A.3
Adams, P.C.4
-
13
-
-
0032729592
-
Significance of linkage disequilibrium between mutation C282Y and an Msel polymorphism in population screening and DNA diagnosis of hemochromatosis
-
deVilliers JNP, Kotze M. Significance of linkage disequilibrium between mutation C282Y and an Msel polymorphism in population screening and DNA diagnosis of hemochromatosis. Blood Cells Mol Dis 1999;25: 250-252.
-
(1999)
Blood Cells Mol Dis
, vol.25
, pp. 250-252
-
-
DeVilliers, J.N.P.1
Kotze, M.2
-
14
-
-
0008266874
-
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
-
Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, et al. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nat Genet 1999;23: 271.
-
(1999)
Nat Genet
, vol.23
, pp. 271
-
-
Merryweather-Clarke, A.T.1
Pointon, J.J.2
Shearman, J.D.3
Robson, K.J.4
Jouanolle, A.M.5
Mosser, A.6
David, V.7
-
15
-
-
0008266874
-
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
-
Noll WW, Belloni DR, Stenzel TT, Grody WW. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nat Genet 1999;23:271-272.
-
(1999)
Nat Genet
, vol.23
, pp. 271-272
-
-
Noll, W.W.1
Belloni, D.R.2
Stenzel, T.T.3
Grody, W.W.4
-
16
-
-
0033229571
-
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
-
Gomez PS, Parks S, Ries R, Tran TC, Gomez PF, Press RD. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nat Genet 1999;23:272.
-
(1999)
Nat Genet
, vol.23
, pp. 272
-
-
Gomez, P.S.1
Parks, S.2
Ries, R.3
Tran, T.C.4
Gomez, P.F.5
Press, R.D.6
-
17
-
-
0033365536
-
An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis
-
Somerville MJ, Sprysak KA, Hicks M, Elyas BG, Vicen-Wyhony L. An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis. Am J Hum Genet 1999;65:924-926.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 924-926
-
-
Somerville, M.J.1
Sprysak, K.A.2
Hicks, M.3
Elyas, B.G.4
Vicen-Wyhony, L.5
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