-
3
-
-
0033966158
-
Iron overload in cirrhosis - HFE genotypes and outcome after liver transplantation
-
Brandhagen DJ, Alvarez W, Therneau TM et al. Iron overload in cirrhosis - HFE genotypes and outcome after liver transplantation. Hepatology 2000; 31: 456-460.
-
(2000)
Hepatology
, vol.31
, pp. 456-460
-
-
Brandhagen, D.J.1
Alvarez, W.2
Therneau, T.M.3
-
4
-
-
0032692722
-
Insulin resistance-associated hepatic iron overload
-
Mendler MH, Turlin B, Moirand R et al. Insulin resistance-associated hepatic iron overload. Gastroenterology 1999; 117: 1155-1163.
-
(1999)
Gastroenterology
, vol.117
, pp. 1155-1163
-
-
Mendler, M.H.1
Turlin, B.2
Moirand, R.3
-
5
-
-
0034883430
-
HFE mutations, iron deficiency and overload in 10 500 blood donors
-
Jackson HA, Carter K, Darke C et al. HFE mutations, iron deficiency and overload in 10 500 blood donors. British Journal of Haematology 2001; 114: 474-484.
-
(2001)
British Journal of Haematology
, vol.114
, pp. 474-484
-
-
Jackson, H.A.1
Carter, K.2
Darke, C.3
-
6
-
-
0037132786
-
Penetrance of 845G-A(C282Y) HFE hereditary haemochromatosis mutation in the USA
-
Beutler E, Felitti VJ, Koziol JA et al. 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
-
8
-
-
0018185564
-
The measurement of total and unsaturated iron binding capacity in serum
-
International Committee for Standardisation in Haematology
-
International Committee for Standardisation in Haematology. The measurement of total and unsaturated iron binding capacity in serum. British Journal of Haematology 1978; 38: 281-290.
-
(1978)
British Journal of Haematology
, vol.38
, pp. 281-290
-
-
-
9
-
-
0006586377
-
Determination of serum iron and total iron-binding capacity: Proposed standard H17-P
-
National Committee for Clinical Laboratory Standards (NCCLS) Villanova, PA: NCCLS
-
National Committee for Clinical Laboratory Standards (NCCLS). Determination of serum iron and total iron-binding capacity: proposed standard H17-P. Villanova, PA: NCCLS, 1990.
-
(1990)
-
-
-
10
-
-
0031992789
-
Transferrin saturation and screening of genetic haemochromatosis
-
Vernet M & LeGall JY. Transferrin saturation and screening of genetic haemochromatosis. Clinical Chemistry 1998; 44: 360-361.
-
(1998)
Clinical Chemistry
, vol.44
, pp. 360-361
-
-
Vernet, M.1
LeGall, J.Y.2
-
11
-
-
0029029626
-
Screening blood donors for hereditary hemochromatosis: Decision analysis model based on a 30-year database
-
Adams PC, Gregor JC, Kertesz AE & Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database. Gastroenterology 1995; 109: 177-188.
-
(1995)
Gastroenterology
, vol.109
, pp. 177-188
-
-
Adams, P.C.1
Gregor, J.C.2
Kertesz, A.E.3
Valberg, L.S.4
-
12
-
-
0034027405
-
Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis
-
Hickman PE, Hourigan LF, Powell LW et al. Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis. Gut 2000; 46: 405-409.
-
(2000)
Gut
, vol.46
, pp. 405-409
-
-
Hickman, P.E.1
Hourigan, L.F.2
Powell, L.W.3
-
13
-
-
0029021768
-
Extremely elevated serum ferritin levels in a University Hospital: Associated diseases and clinical significance
-
Lee MH & Means RT. Extremely elevated serum ferritin levels in a University Hospital: associated diseases and clinical significance. American Journal of Medicine 1995; 98: 566-571.
-
(1995)
American Journal of Medicine
, vol.98
, pp. 566-571
-
-
Lee, M.H.1
Means, R.T.2
-
15
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis
-
Feder JN, Gnirke A, Thomas W et al. A novel MHC class I-like gene is mutated in patients with hereditary hemochromatosis. Nature Genetics 1996; 13: 399-408.
-
(1996)
Nature Genetics
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
-
16
-
-
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. Nature Genetics 1999; 22: 325-326.
-
(1999)
Nature Genetics
, vol.22
, pp. 325-326
-
-
Jeffrey, G.P.1
Chakrabarti, S.2
Hegele, R.A.3
Adams, P.C.4
-
17
-
-
0008266874
-
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
-
Merryweather-Clarke AT, Pointon JJ, Shearman JD et al. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Nature Genetics 1999; 23: 271-272.
-
(1999)
Nature Genetics
, vol.23
, pp. 271-272
-
-
Merryweather-Clarke, A.T.1
Pointon, J.J.2
Shearman, J.D.3
-
18
-
-
0005600868
-
A simple genetic test identifies 90% of UK patients with haemochromatosis
-
The UK Haemochromatosis Consortium
-
The 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
-
-
-
19
-
-
0032955556
-
Molecular medicine and hemochromatosis: At the crossroads
-
Bacon BR, Powell LW, Adams PC et al. 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
-
20
-
-
0036107538
-
Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y
-
Wallace DF, Walker AP, Pietrangelo A et al. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y. Journal of Hepatology 2002; 36: 474-479.
-
(2002)
Journal of Hepatology
, vol.36
, pp. 474-479
-
-
Wallace, D.F.1
Walker, A.P.2
Pietrangelo, A.3
-
21
-
-
0022656390
-
Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis
-
Bassett ML, Halliday JW & Powell LW. Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis. Hepatology 1986; 6: 24-29.
-
(1986)
Hepatology
, vol.6
, pp. 24-29
-
-
Bassett, M.L.1
Halliday, J.W.2
Powell, L.W.3
-
22
-
-
0034856294
-
Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL conference
-
Bruix J, Sherman M, Llovet JM et al. Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL conference. Journal of Hepatology 2001; 35: 421-430.
-
(2001)
Journal of Hepatology
, vol.35
, pp. 421-430
-
-
Bruix, J.1
Sherman, M.2
Llovet, J.M.3
-
23
-
-
0033054006
-
Elevated serum type IV collagen: A sensitive indicator for the presence of cirrhosis in haemochromatosis
-
George DK, Ramm GA, Walker NI et al. Elevated serum type IV collagen: a sensitive indicator for the presence of cirrhosis in haemochromatosis. Journal of Hepatology 1999; 31: 47-52.
-
(1999)
Journal of Hepatology
, vol.31
, pp. 47-52
-
-
George, D.K.1
Ramm, G.A.2
Walker, N.I.3
-
24
-
-
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
-
25
-
-
33645185630
-
Guidelines on diagnosis and treatment
-
British Committee for Standards in Haematology www.bcshguidelines.com/ (see under Haemato Oncology)
-
British Committee for Standards in Haematology. Guidelines on diagnosis and treatment. Genetic Haemochromatosis. www.bcshguidelines.com/ (see under Haemato Oncology) 2000; 13-14.
-
(2000)
Genetic Haemochromatosis
, pp. 13-14
-
-
-
26
-
-
0033564146
-
HFE genotype in patients with hemochromatosis and other liver diseases
-
Bacon BR, Olynyk JK, Brunt EM et al. HFE genotype in patients with hemochromatosis and other liver diseases. Annals of Internal Medicine 1999; 130: 953-962.
-
(1999)
Annals of Internal Medicine
, vol.130
, pp. 953-962
-
-
Bacon, B.R.1
Olynyk, J.K.2
Brunt, E.M.3
-
27
-
-
0035038147
-
Diagnosis and management of hemochromatosis
-
Tavill AS. Diagnosis and management of hemochromatosis. Hepatology 2001; 33: 1321-1328.
-
(2001)
Hepatology
, vol.33
, pp. 1321-1328
-
-
Tavill, A.S.1
-
28
-
-
0002717328
-
Computed tomography and magnetic resonance imaging in the diagnosis of hemochromatosis
-
Barton JC & Edwards CO (eds) Cambridge: Cambridge University Press
-
Guyader D & Gandon Y. Computed tomography and magnetic resonance imaging in the diagnosis of hemochromatosis. In Barton JC & Edwards CO (eds) Hemochromatosis: genetics, pathophysiology, diagnoses and treatment pp 219-225. Cambridge: Cambridge University Press, 2000.
-
(2000)
Hemochromatosis: Fenetics, Pathophysiology, Diagnoses and Treatment
, pp. 219-225
-
-
Guyader, D.1
Gandon, Y.2
-
31
-
-
0033795335
-
HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis
-
Distante S, Berg JP, Lande K et al. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis. Gut 2000; 47: 575-579.
-
(2000)
Gut
, vol.47
, pp. 575-579
-
-
Distante, S.1
Berg, J.P.2
Lande, K.3
-
32
-
-
0034022636
-
The gene TRF2 is mutated in a new type of haemochromatosis mapping to 7q22
-
Camaschella C, Roetto A, Cali A et al. The gene TRF2 is mutated in a new type of haemochromatosis mapping to 7q22. Nature Genetics 2000; 25: 14-15.
-
(2000)
Nature Genetics
, vol.25
, pp. 14-15
-
-
Camaschella, C.1
Roetto, A.2
Cali, A.3
-
33
-
-
0035353167
-
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
-
Roetto A, Totaro A, Piperno A et al. New mutations inactivating transferrin receptor 2 in hemochromatosis type 3. Blood 2001; 917: 2555-2560.
-
(2001)
Blood
, vol.917
, pp. 2555-2560
-
-
Roetto, A.1
Totaro, A.2
Piperno, A.3
-
34
-
-
0034964604
-
A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload
-
Kato J, Fujikawa K, Kanda M et al. A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload. American Journal of Human Genetics 2001; 69: 191-197.
-
(2001)
American Journal of Human Genetics
, vol.69
, pp. 191-197
-
-
Kato, J.1
Fujikawa, K.2
Kanda, M.3
-
35
-
-
17944380796
-
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLCIIA3) gene
-
Montosi G, Donovan A, Totaro A et al. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLCIIA3) gene. Journal of Clinical Investigation 200 1; 108: 619-623.
-
(2001)
Journal of Clinical Investigation
, vol.108
, pp. 619-623
-
-
Montosi, G.1
Donovan, A.2
Totaro, A.3
-
36
-
-
0034930197
-
A mutation in SLCIIA3 is associated with autosomal dominant hemochromatosis
-
Njajou OT, Vaessen N, Joosse M et al. A mutation in SLCIIA3 is associated with autosomal dominant hemochromatosis. Nature Genetics 2001; 28: 213-214.
-
(2001)
Nature Genetics
, vol.28
, pp. 213-214
-
-
Njajou, O.T.1
Vaessen, N.2
Joosse, M.3
-
37
-
-
0037100382
-
Autosomal dominant reticulo-endothelial iron overload associated with a three base pair deletion in the ferroportin I gene (SLCIIA3)
-
Devalia V, Carter K, Walker AP et al. Autosomal dominant reticulo-endothelial iron overload associated with a three base pair deletion in the ferroportin I gene (SLCIIA3). Blood 2002; 100: 715-717.
-
(2002)
Blood
, vol.100
, pp. 715-717
-
-
Devalia, V.1
Carter, K.2
Walker, A.P.3
-
38
-
-
0033848697
-
EASL International Consensus Conference on Haemochromatosis
-
Adams P, Brissot P & Powell LW. EASL International Consensus Conference on Haemochromatosis. Journal of Hepatology 2000; 33: 485-504.
-
(2000)
Journal of Hepatology
, vol.33
, pp. 485-504
-
-
Adams, P.1
Brissot, P.2
Powell, L.W.3
-
40
-
-
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 et al. Hemochromatosis-associated mortality in the United States from 1979 to 1992: an analysis of multiple-cause mortality data. Annals of Internal Medicine 1998; 129: 946-953.
-
(1998)
Annals of Internal Medicine
, vol.129
, pp. 946-953
-
-
Yang, Q.1
McDonnell, S.M.2
Khoury, M.J.3
-
41
-
-
0031839335
-
The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population
-
Merryweather-Clarke AT, Worwood M, Parkinson L et al. The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population. British Journal of Haematology 101; 369-373.
-
British Journal of Haematology
, vol.101
, pp. 369-373
-
-
Merryweather-Clarke, A.T.1
Worwood, M.2
Parkinson, L.3
-
42
-
-
4243885234
-
Population screening for hemochromatosis: A comparison of unbound iron binding capacity, transferrin saturation and C282Y genotyping in 5,211 voluntary blood donors
-
(Abstract)
-
Adams PC, Kertesz AE, McLaren C et al. Population screening for hemochromatosis: a comparison of unbound iron binding capacity, transferrin saturation and C282Y genotyping in 5,211 voluntary blood donors. Hepatology 1999; 30: 502A (Abstract).
-
(1999)
Hepatology
, vol.30
-
-
Adams, P.C.1
Kertesz, A.E.2
McLaren, C.3
-
43
-
-
0032401707
-
Prevalence of hereditary hemochromatosis in 16,031 primary care patients
-
Phatak PD, Sham RL, Raubertas RF et al. Prevalence of hereditary hemochromatosis in 16,031 primary care patients. Annals of Internal Medicine 1998; 129: 954-961.
-
(1998)
Annals of Internal Medicine
, vol.129
, pp. 954-961
-
-
Phatak, P.D.1
Sham, R.L.2
Raubertas, R.F.3
-
44
-
-
0027080655
-
Does transplantation of the liver cure haemochromatosis
-
Powell LW. Does transplantation of the liver cure haemochromatosis. Journal of Hepatology 1992; 16: 259-261.
-
(1992)
Journal of Hepatology
, vol.16
, pp. 259-261
-
-
Powell, L.W.1
-
45
-
-
0031450438
-
Haemochromatosis, HFE and genetic complexity
-
Risch N. Haemochromatosis, HFE and genetic complexity. Nature Genetics 1997; 17: 375-376.
-
(1997)
Nature Genetics
, vol.17
, pp. 375-376
-
-
Risch, N.1
-
46
-
-
0031944939
-
Implications of genotyping of spouses to limit investigation in children in genetic haemochromatosis
-
Adams PC. Implications of genotyping of spouses to limit investigation in children in genetic haemochromatosis. Clinical Genetics 1998; 53: 176-178.
-
(1998)
Clinical Genetics
, vol.53
, pp. 176-178
-
-
Adams, P.C.1
-
49
-
-
0029863455
-
Hemochromatosis: The impact of early diagnosis and therapy
-
Powell LW. Hemochromatosis: the impact of early diagnosis and therapy. Gastroenterology 1996; 110: 1304-1307.
-
(1996)
Gastroenterology
, vol.110
, pp. 1304-1307
-
-
Powell, L.W.1
-
50
-
-
0033833865
-
Juvenile hemochromatosis associated with β-thalassemia treated by phlebotomy and recombinant human erythropoietin
-
De Gobbi M, Pasquero P, Brunello F et al. Juvenile hemochromatosis associated with β-thalassemia treated by phlebotomy and recombinant human erythropoietin. Haematologica 2000; 85: 865-867.
-
(2000)
Haematologica
, vol.85
, pp. 865-867
-
-
De Gobbi, M.1
Pasquero, P.2
Brunello, F.3
-
51
-
-
0022368621
-
Survival and causes of death in cirrhotic and in non-cirrhotic patients with hemochromatosis
-
Niederau C, Fischer R, Sonnenberg A et al. Survival and causes of death in cirrhotic and in non-cirrhotic patients with hemochromatosis. New England Journal of Medicine 1985; 313: 1256-1262.
-
(1985)
New England Journal of Medicine
, vol.313
, pp. 1256-1262
-
-
Niederau, C.1
Fischer, R.2
Sonnenberg, A.3
-
52
-
-
0027987205
-
Prognostic factors for hepatocellular carcinoma in genetic hemochromatosis
-
Fargion S, Fracanzani AL, Piperno A et al. Prognostic factors for hepatocellular carcinoma in genetic hemochromatosis. Hepatology 1994; 20: 1426-1431.
-
(1994)
Hepatology
, vol.20
, pp. 1426-1431
-
-
Fargion, S.1
Fracanzani, A.L.2
Piperno, A.3
-
53
-
-
0027989911
-
Outcome of liver transplantation in patients with haemochromatosis
-
Farrell FJ, Nguyen M, Woodley S et al. Outcome of liver transplantation in patients with haemochromatosis. Hepatology 1994; 20: 404-410.
-
(1994)
Hepatology
, vol.20
, pp. 404-410
-
-
Farrell, F.J.1
Nguyen, M.2
Woodley, S.3
-
54
-
-
0034883875
-
Liver transplantation for hereditary hemochromatosis
-
Brandhagen DJ. Liver transplantation for hereditary hemochromatosis. Liver Transplantation 2001; 7: 663-672.
-
(2001)
Liver Transplantation
, vol.7
, pp. 663-672
-
-
Brandhagen, D.J.1
-
55
-
-
0026087634
-
Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: Polygraphic and echocardiographic evaluation
-
Cecchetti G, Binda A, Piperno A et al. Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: polygraphic and echocardiographic evaluation. European Heart Journal 1991; 12: 224-230.
-
(1991)
European Heart Journal
, vol.12
, pp. 224-230
-
-
Cecchetti, G.1
Binda, A.2
Piperno, A.3
-
56
-
-
0024554054
-
Osteoporosis in hemochromatosis: Iron excess, gonadal deficiency, or other factors?
-
Diamond T, Stiehl D & Posen S. Osteoporosis in hemochromatosis: iron excess, gonadal deficiency, or other factors? Annals of Internal Medicine 1989; 110: 430-436.
-
(1989)
Annals of Internal Medicine
, vol.110
, pp. 430-436
-
-
Diamond, T.1
Stiehl, D.2
Posen, S.3
-
57
-
-
0026490494
-
Osteoporotic fractures: An unusual presentation of haemochromatosis
-
Eyres KS, McClasky EV, Fern ED et al. Osteoporotic fractures: an unusual presentation of haemochromatosis. Bone 1992; 13: 431-433.
-
(1992)
Bone
, vol.13
, pp. 431-433
-
-
Eyres, K.S.1
McClasky, E.V.2
Fern, E.D.3
-
58
-
-
0033652251
-
Etidronate for osteoporosis in primary biliary cirrhosis: A randomised trial
-
Lindor KD, Jorgensen RA, Tiegs RD et al. Etidronate for osteoporosis in primary biliary cirrhosis: a randomised trial. Journal of Hepatology 2000; 33: 878-882.
-
(2000)
Journal of Hepatology
, vol.33
, pp. 878-882
-
-
Lindor, K.D.1
Jorgensen, R.A.2
Tiegs, R.D.3
-
59
-
-
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: 724-727.
-
(1996)
Hepatology
, vol.23
, pp. 724-727
-
-
Adams, P.C.1
Agnew, S.2
|