-
1
-
-
0028053928
-
Epidemiology, clinical spectrum and prognosis of hemochromatosis
-
Niederau C, Strohmeyer G, Stremmel W. Epidemiology, clinical spectrum and prognosis of hemochromatosis. Adv Exp Med Biol 1994;356:293-302.
-
(1994)
Adv Exp Med Biol
, vol.356
, pp. 293-302
-
-
Niederau, C.1
Strohmeyer, G.2
Stremmel, W.3
-
3
-
-
0031836302
-
Classification and diagnosis of iron overload
-
Piperno A. Classification and diagnosis of iron overload. Hematologica 1998;83:447-55.
-
(1998)
Hematologica
, vol.83
, pp. 447-455
-
-
Piperno, A.1
-
4
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder JN, Gnirke A, Thomas W, 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
-
5
-
-
17644434333
-
The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression
-
Feder JN, Tsuchihashi Z, Irrinki A, et al. The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression. J Biol Chem 1997;272: 14025-8.
-
(1997)
J Biol Chem
, vol.272
, pp. 14025-14028
-
-
Feder, J.N.1
Tsuchihashi, Z.2
Irrinki, A.3
-
6
-
-
0030732164
-
Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells
-
Waheed A, Parkkila S, Zhou XY, et al. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proc Natl Acad Sci U S A 1997;94:12384-9.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 12384-12389
-
-
Waheed, A.1
Parkkila, S.2
Zhou, X.Y.3
-
7
-
-
0030221927
-
Mutation analysis in hereditary hemochromatosis
-
Beutler E, Gelbart T, West C, et al. Mutation analysis in hereditary hemochromatosis. Blood Cells Mol Dis 1996;22:187-94.
-
(1996)
Blood Cells Mol Dis
, vol.22
, pp. 187-194
-
-
Beutler, E.1
Gelbart, T.2
West, C.3
-
9
-
-
0032496881
-
Hereditary hemochromatosis: Gene discovery and its implication for population-based screening
-
Burke W, Thomson E, Koury MJ, et al. Hereditary hemochromatosis: gene discovery and its implication for population-based screening. JAMA 1998;280:172-8.
-
(1998)
JAMA
, vol.280
, pp. 172-178
-
-
Burke, W.1
Thomson, E.2
Koury, M.J.3
-
10
-
-
0031419386
-
A candidate gene for hemochromatosis: Frequency of the C282Y and H63D mutations
-
Jouanolle AM, Fergelot P, Gandon G, et al. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations. Hum Genet 1997;100:544-7.
-
(1997)
Hum Genet
, vol.100
, pp. 544-547
-
-
Jouanolle, A.M.1
Fergelot, P.2
Gandon, G.3
-
11
-
-
0032988517
-
Genotyping as a diagnostic aid in genetic haemochromatosis
-
Rossi E, Henderson S, Chin CY, et al. Genotyping as a diagnostic aid in genetic haemochromatosis. J Gastroenterol Hepatol 1999;14:427-30.
-
(1999)
J Gastroenterol Hepatol
, vol.14
, pp. 427-430
-
-
Rossi, E.1
Henderson, S.2
Chin, C.Y.3
-
12
-
-
0030814039
-
Genetic and clinical description of hemochromatosis probands and heterozygotes: Evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis
-
Barton JC, Shih W, Hirai J, et al. Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis. Blood Cells Mol Dis 1997;23:135-45.
-
(1997)
Blood Cells Mol Dis
, vol.23
, pp. 135-145
-
-
Barton, J.C.1
Shih, W.2
Hirai, J.3
-
13
-
-
0033561342
-
HFE mutations analysis in 711 hemochromatosis probands: Evidence for S65C implication in mild form of hemochromatosis
-
Mura C, Raguénes O, Férec C. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis. Blood 1999;93:2502-5.
-
(1999)
Blood
, vol.93
, pp. 2502-2505
-
-
Mura, C.1
Raguénes, O.2
Férec, C.3
-
14
-
-
0033150066
-
Two novel missense mutations of the HFE gene (1105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands
-
Barton JC, Sawada-Hirai R, Rothenberg BE, et al. Two novel missense mutations of the HFE gene (1105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands. Blood Cells Mol Dis 1997;25:147-55.
-
(1997)
Blood Cells Mol Dis
, vol.25
, pp. 147-155
-
-
Barton, J.C.1
Sawada-Hirai, R.2
Rothenberg, B.E.3
-
15
-
-
0035425811
-
HFE gene and hereditary hemochromatosis: A HuGE review
-
Hanson EH, Imperatore G, Burke W. HFE gene and hereditary hemochromatosis: a HuGE review. Am J Epidemiol 2001;154: 193-206.
-
(2001)
Am J Epidemiol
, vol.154
, pp. 193-206
-
-
Hanson, E.H.1
Imperatore, G.2
Burke, W.3
-
16
-
-
0037164344
-
Genetics of haemochromatosis
-
Bomford A. Genetics of haemochromatosis. Lancet 2002;360: 1673-81.
-
(2002)
Lancet
, vol.360
, pp. 1673-1681
-
-
Bomford, A.1
-
17
-
-
0033517343
-
A population-based study of the clinical expression of the hemochromatosis gene
-
Olynyk JK, Cullen DJ, Aquilia S, et al. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med 1999;341:718-24.
-
(1999)
N Engl J Med
, vol.341
, pp. 718-724
-
-
Olynyk, J.K.1
Cullen, D.J.2
Aquilia, S.3
-
19
-
-
0031927156
-
Hemochromatosis: Genetics helps to define a multifactorial disease
-
Burke W, Press N, McDonnell SM. Hemochromatosis: genetics helps to define a multifactorial disease. Clin Genet 1998;54:1-9.
-
(1998)
Clin Genet
, vol.54
, pp. 1-9
-
-
Burke, W.1
Press, N.2
McDonnell, S.M.3
-
20
-
-
0027095744
-
Liver damage in Italian patients with hereditary hemochromatosis is highly influenced by hepatitis B and C virus infection
-
Piperno A, Fargion S, D'Alba R, et al. Liver damage in Italian patients with hereditary hemochromatosis is highly influenced by hepatitis B and C virus infection. J Hepatol 1992;16:364-8.
-
(1992)
J Hepatol
, vol.16
, pp. 364-368
-
-
Piperno, A.1
Fargion, S.2
D'Alba, R.3
-
21
-
-
0031433062
-
Phenotype-genotype correlation in haemochromatosis subjects
-
Mura C, Nousbaum JB, Verger P, et al. Phenotype-genotype correlation in haemochromatosis subjects. Hum Genet 1997; 101:271-6.
-
(1997)
Hum Genet
, vol.101
, pp. 271-276
-
-
Mura, C.1
Nousbaum, J.B.2
Verger, P.3
-
22
-
-
0034859463
-
Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC
-
Le Gac G, Mura C, Férec C. Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC. Clin Chem 2001;47:1633-40.
-
(2001)
Clin Chem
, vol.47
, pp. 1633-1640
-
-
Le Gac, G.1
Mura, C.2
Férec, C.3
-
23
-
-
0026732182
-
Liver fibrosis in genetic hemochromatosis respective roles of iron and non-iron-related factors in 127 homozygous patients
-
Loréal O, Deugnier Y, Moirand R, et al. Liver fibrosis in genetic hemochromatosis respective roles of iron and non-iron-related factors in 127 homozygous patients. J Hepatol 1992;16: 122-7.
-
(1992)
J Hepatol
, vol.16
, pp. 122-127
-
-
Loréal, O.1
Deugnier, Y.2
Moirand, R.3
-
25
-
-
0029927660
-
Alcoholism in hereditary hemochromatosis revisited: Prevalence and clinical consequences among homozygous siblings
-
Adams PC, Agnew S. Alcoholism in hereditary hemochromatosis revisited: prevalence and clinical consequences among homozygous siblings. Hepatology 1996;23:724-7.
-
(1996)
Hepatology
, vol.23
, pp. 724-727
-
-
Adams, P.C.1
Agnew, S.2
-
26
-
-
0027243247
-
Validity and reliability of self-reported drinking behavior: Dealing with the problem of response bias
-
Embree BG, Whitehead PC. Validity and reliability of self-reported drinking behavior: dealing with the problem of response bias. J Stud Alcohol 1993;54:334-44.
-
(1993)
J Stud Alcohol
, vol.54
, pp. 334-344
-
-
Embree, B.G.1
Whitehead, P.C.2
-
27
-
-
0036774940
-
Concurrent validity of alcohol consumption measurement in a "healthy" population; quantity questionnaire v. dietary historian interview
-
Koppes LL, Twisk JW, Snel J, et al. Concurrent validity of alcohol consumption measurement in a "healthy" population; quantity questionnaire v. dietary historian interview. Br J Nutr 2002;88:427-34.
-
(2002)
Br J Nutr
, vol.88
, pp. 427-434
-
-
Koppes, L.L.1
Twisk, J.W.2
Snel, J.3
-
28
-
-
0036163634
-
Excess alcohol greatly increases the prevalence of cirrhosis in hereditary hemochromatosis
-
Fletcher LM, Dixon JL, Purdie DM, et al. Excess alcohol greatly increases the prevalence of cirrhosis in hereditary hemochromatosis. Gastroenterology 2002;122:281-9.
-
(2002)
Gastroenterology
, vol.122
, pp. 281-289
-
-
Fletcher, L.M.1
Dixon, J.L.2
Purdie, D.M.3
-
29
-
-
0036161159
-
Hereditary hemochromatosis and alcohol: A fibrogenic cocktail
-
Britton RS, Bacon ER. Hereditary hemochromatosis and alcohol: a fibrogenic cocktail. Gastroenterology 2002;122:563-5.
-
(2002)
Gastroenterology
, vol.122
, pp. 563-565
-
-
Britton, R.S.1
Bacon, E.R.2
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