-
2
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder NJ, 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, N.J.1
Gnirke, A.2
Thomas, W.3
-
3
-
-
0031793132
-
The significance of haemochromatosis gene mutations in the general population: Implications for screening
-
Burt MJ, George PM, Upton JD, et al. The significance of haemochromatosis gene mutations in the general population: implications for screening. Gut. 1998;43:830-836.
-
(1998)
Gut
, vol.43
, pp. 830-836
-
-
Burt, M.J.1
George, P.M.2
Upton, J.D.3
-
4
-
-
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
-
5
-
-
0030221927
-
Mutation analysis in hereditary hemochromatosis
-
Beutler E, Gelbart T, West C, et al. Mutation analysis in hereditary hemochromatosis. Blood Cells Mol Dis. 1996;22:187-194.
-
(1996)
Blood Cells Mol Dis
, vol.22
, pp. 187-194
-
-
Beutler, E.1
Gelbart, T.2
West, C.3
-
8
-
-
0030864560
-
Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families
-
Adams PC, Campion ML, Gandon G, LeGall JY, David V, Jouanolle AM. Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families. Hepatology. 1997;26:986-990.
-
(1997)
Hepatology
, vol.26
, pp. 986-990
-
-
Adams, P.C.1
Campion, M.L.2
Gandon, G.3
LeGall, J.Y.4
David, V.5
Jouanolle, A.M.6
-
9
-
-
0005600868
-
A simple genetic test identifies 90% of UK patients with haemochromatosis
-
UK Haemochromatosis Consortium. A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut. 1997;41: 841-844.
-
(1997)
Gut
, vol.41
, pp. 841-844
-
-
-
10
-
-
0032927124
-
Phenotypic expression of HFE mutations: A French study of 1110 unrelated iron-overloaded patients and relatives
-
Moirand R, Jouanolle AM, Brissot P, LeGall JY, David V, Deugnier Y. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives. Gastroenterology. 1999;116:372-377.
-
(1999)
Gastroenterology
, vol.116
, pp. 372-377
-
-
Moirand, R.1
Jouanolle, A.M.2
Brissot, P.3
LeGall, J.Y.4
David, V.5
Deugnier, Y.6
-
11
-
-
0036177909
-
A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation
-
Gochee P, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation [published correction appears in Gastroenterology. 2002;122:1191]. Gastroenterology. 2002;122:646-651.
-
(2002)
Gastroenterology
, vol.122
, pp. 646-651
-
-
Gochee, P.1
Powell, L.W.2
Cullen, D.J.3
Du Sart, D.4
Rossi, E.5
Olynyk, J.K.6
-
12
-
-
85050706101
-
-
published correction appears
-
Gochee P, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation [published correction appears in Gastroenterology. 2002;122:1191]. Gastroenterology. 2002;122:646-651.
-
(2002)
Gastroenterology
, vol.122
, pp. 1191
-
-
-
13
-
-
0032955556
-
Molecular medicine and hemochromatosis: At the crossroads
-
Bacon BR, Powell LW, Adams PC, Kresina TF, Hoofnagle JH. Molecular medicine and hemochromatosis: at the crossroads. Gastroenterology. 1999;116:193-207.
-
(1999)
Gastroenterology
, vol.116
, pp. 193-207
-
-
Bacon, B.R.1
Powell, L.W.2
Adams, P.C.3
Kresina, T.F.4
Hoofnagle, J.H.5
-
14
-
-
0042793519
-
Penetrance of hemochromatosis
-
Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E. Penetrance of hemochromatosis. Blood Cells Mol Dis. 2002;29:418-432.
-
(2002)
Blood Cells Mol Dis
, vol.29
, pp. 418-432
-
-
Waalen, J.1
Felitti, V.2
Gelbart, T.3
Ho, N.J.4
Beutler, E.5
-
15
-
-
17944369464
-
Screening for hemochromatosis: High prevalence and low morbidity in an unselected population of 65,238 persons
-
Asberg A, Hveem K, Thorstensen K, et al. Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons. Scand J Gastroenterol. 2001;36:1108-1115.
-
(2001)
Scand J Gastroenterol
, vol.36
, pp. 1108-1115
-
-
Asberg, A.1
Hveem, K.2
Thorstensen, K.3
-
16
-
-
0036944167
-
Hereditary haemochromatosis: Only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload
-
McCune CA, Al-Jader LN, May A, Hayes SL, Jackson HA, Worwood M. Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload. Hum Genet. 2002;111:538-543.
-
(2002)
Hum Genet
, vol.111
, pp. 538-543
-
-
McCune, C.A.1
Al-Jader, L.N.2
May, A.3
Hayes, S.L.4
Jackson, H.A.5
Worwood, M.6
-
17
-
-
0037132786
-
Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA
-
Beutler E, Felitti VJ, Koziol JA, Ho NJ, Gelbart T. Penetrance of 845G→A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Lancet. 2002;359:211-218.
-
(2002)
Lancet
, vol.359
, pp. 211-218
-
-
Beutler, E.1
Felitti, V.J.2
Koziol, J.A.3
Ho, N.J.4
Gelbart, T.5
-
18
-
-
0014401225
-
Diabetes detected by blood-sugar measurement after a glucose load: Report from the Busselton survey, 1966
-
Welborn TA, Curnow DH, Wearne JT, Cullen KJ, McCall MG, Stenhouse NS. Diabetes detected by blood-sugar measurement after a glucose load: report from the Busselton survey, 1966. Med J Aust. 1968;2:778-783.
-
(1968)
Med J Aust
, vol.2
, pp. 778-783
-
-
Welborn, T.A.1
Curnow, D.H.2
Wearne, J.T.3
Cullen, K.J.4
McCall, M.G.5
Stenhouse, N.S.6
-
19
-
-
0030710191
-
Prediction of coronary heart disease mortality in Busselton, Western Australia: An evaluation of the Framingham, national health epidemiologic follow up study, and WHO ERICA risk scores
-
Knuiman MW, Vu HT. Prediction of coronary heart disease mortality in Busselton, Western Australia: an evaluation of the Framingham, national health epidemiologic follow up study, and WHO ERICA risk scores. J Epidemiol Community Health. 1997; 51:515-519.
-
(1997)
J Epidemiol Community Health
, vol.51
, pp. 515-519
-
-
Knuiman, M.W.1
Vu, H.T.2
-
20
-
-
0037481178
-
Serum ferritin and cardiovascular disease: A 17-year follow-up study in Busselton, Western Australia
-
Knuiman MW, Divitini ML, Olynyk JK, Cullen DJ, Bartholomew HC. Serum ferritin and cardiovascular disease: a 17-year follow-up study in Busselton, Western Australia. Am J Epidemiol. 2003;158:144-149.
-
(2003)
Am J Epidemiol
, vol.158
, pp. 144-149
-
-
Knuiman, M.W.1
Divitini, M.L.2
Olynyk, J.K.3
Cullen, D.J.4
Bartholomew, H.C.5
-
21
-
-
0035801682
-
High prevalence of coeliac disease in a population-based study from Western Australia: A case for screening?
-
Hovell CJ, Collett JA, Vautier G, et al. High prevalence of coeliac disease in a population-based study from Western Australia: a case for screening? Med J Aust. 2001;175:247-250.
-
(2001)
Med J Aust
, vol.175
, pp. 247-250
-
-
Hovell, C.J.1
Collett, J.A.2
Vautier, G.3
-
22
-
-
18544376989
-
Gender-specific phenotypic expression and screening strategies in C282Y-linked hemochromatosis: A study of 9396 French people
-
Deugnier Y, Jouanolle AM, Chaperon J, et al. Gender-specific phenotypic expression and screening strategies in C282Y-linked hemochromatosis: a study of 9396 French people. Br J Haematol. 2002;118:1170-1178.
-
(2002)
Br J Haematol
, vol.118
, pp. 1170-1178
-
-
Deugnier, Y.1
Jouanolle, A.M.2
Chaperon, J.3
-
23
-
-
0141961623
-
Natural history of the C282Y homozygote for the hemochromatosis gene (HFE) with a normal serum ferritin level
-
Yamashita C, Adams PC. Natural history of the C282Y homozygote for the hemochromatosis gene (HFE) with a normal serum ferritin level. Clin Gastroenterol Hepatol. 2003;1:388-391.
-
(2003)
Clin Gastroenterol Hepatol
, vol.1
, pp. 388-391
-
-
Yamashita, C.1
Adams, P.C.2
-
24
-
-
0001926618
-
Iron absorption
-
Brock JH, Halliday JW, Pippard MJ, Powell LW, eds. London, England: WB Saunders Co.
-
Skikne B, Baynes RD. Iron absorption. In: Brock JH, Halliday JW, Pippard MJ, Powell LW, eds. Iron Metabolism in Health and Disease. London, England: WB Saunders Co; 1994:151-187.
-
(1994)
Iron Metabolism in Health and Disease
, pp. 151-187
-
-
Skikne, B.1
Baynes, R.D.2
-
25
-
-
0033564146
-
HFE genotype in patients with hemochromatosis and other liver diseases
-
Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK. HFE genotype in patients with hemochromatosis and other liver diseases. Ann Intern Med. 1999;130:953-962.
-
(1999)
Ann Intern Med
, vol.130
, pp. 953-962
-
-
Bacon, B.R.1
Olynyk, J.K.2
Brunt, E.M.3
Britton, R.S.4
Wolff, R.K.5
-
26
-
-
0031707469
-
Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis
-
Guyader D, Jacquelinet C, Moirand R, et al. Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis. Gastroenterology. 1998;115:929-936.
-
(1998)
Gastroenterology
, vol.115
, pp. 929-936
-
-
Guyader, D.1
Jacquelinet, C.2
Moirand, R.3
|