-
1
-
-
2542560427
-
Hereditary hemochromatosis - a new look at an old disease
-
Pietrangelo A. Hereditary hemochromatosis - a new look at an old disease. N Engl J Med 2004;350:2383-2397.
-
(2004)
N Engl J Med
, vol.350
, pp. 2383-2397
-
-
Pietrangelo, A.1
-
2
-
-
0002371516
-
Hereditary hemochromatosis
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds, New York, NY: McGraw-Hill;
-
Beutler E, Bothwell TH, Charlron RW, Motulsky AG. Hereditary hemochromatosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease. New York, NY: McGraw-Hill; 2001:3127-3162.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 3127-3162
-
-
Beutler, E.1
Bothwell, T.H.2
Charlron, R.W.3
Motulsky, A.G.4
-
3
-
-
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, 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
-
4
-
-
33144456592
-
Hemochromatosis: Genetics and pathophysiology
-
Beutler E. Hemochromatosis: genetics and pathophysiology. Annu Rev Med 2006;57:331-347.
-
(2006)
Annu Rev Med
, vol.57
, pp. 331-347
-
-
Beutler, E.1
-
5
-
-
34147135182
-
Hereditary hemochromatosis genotypes and risk of ischemic srroke
-
Ellervik C, Tybjaerg-Hansen A, Appleyard M, Sillesen H, Boysen G, Nordesrgaard BG. Hereditary hemochromatosis genotypes and risk of ischemic srroke. Neurology 2007;68:1025-1031.
-
(2007)
Neurology
, vol.68
, pp. 1025-1031
-
-
Ellervik, C.1
Tybjaerg-Hansen, A.2
Appleyard, M.3
Sillesen, H.4
Boysen, G.5
Nordesrgaard, B.G.6
-
9
-
-
0036893631
-
Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C
-
Bonkovsky HL, Troy N, McNeal K, Banner BF, Sharma A, Obando J, et al. Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C. J Hepatol 2002;37:848-854.
-
(2002)
J Hepatol
, vol.37
, pp. 848-854
-
-
Bonkovsky, H.L.1
Troy, N.2
McNeal, K.3
Banner, B.F.4
Sharma, A.5
Obando, J.6
-
10
-
-
28844482171
-
Steatosis is a cofactor in liver injury in hemochromatosis
-
Powell EE, Ali A, Clouston AD, Dixon JL, Lincoln DJ, Purdie DM, et al. Steatosis is a cofactor in liver injury in hemochromatosis. Gastroenterology 2005;129:1937-1943.
-
(2005)
Gastroenterology
, vol.129
, pp. 1937-1943
-
-
Powell, E.E.1
Ali, A.2
Clouston, A.D.3
Dixon, J.L.4
Lincoln, D.J.5
Purdie, D.M.6
-
11
-
-
0038621885
-
Interaction of iron, insulin resistance, and nonalcoholic steatohepatitis
-
Chitturi S, George J. Interaction of iron, insulin resistance, and nonalcoholic steatohepatitis. Curr Gastroenterol Rep 2003;5:18-25.
-
(2003)
Curr Gastroenterol Rep
, vol.5
, pp. 18-25
-
-
Chitturi, S.1
George, J.2
-
12
-
-
28444435827
-
-
Alla V, Bonkovsky HL. Iron in nonhemochromatotic liver disorders. Semin Liver Dis 2005;25:461-472.
-
Alla V, Bonkovsky HL. Iron in nonhemochromatotic liver disorders. Semin Liver Dis 2005;25:461-472.
-
-
-
-
13
-
-
0026498217
-
Hepatitis C virus and porphyria cutanea tarda: Evidence of a strong association
-
Fargion S, Piperno A, Cappellini MD, Sampietro M, Fracanzani AL, Romano R, et al. Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association. HEPATOLOGY 1992;16:1322-1326.
-
(1992)
HEPATOLOGY
, vol.16
, pp. 1322-1326
-
-
Fargion, S.1
Piperno, A.2
Cappellini, M.D.3
Sampietro, M.4
Fracanzani, A.L.5
Romano, R.6
-
14
-
-
0015261886
-
Frequency of occurrence of hepatocellular carcinoma in patients with porphyria cutanea tarda in long-term follow-up
-
Kordac V. Frequency of occurrence of hepatocellular carcinoma in patients with porphyria cutanea tarda in long-term follow-up. Neoplasma 1972;19:135-139.
-
(1972)
Neoplasma
, vol.19
, pp. 135-139
-
-
Kordac, V.1
-
15
-
-
33645326193
-
Iron dysregulation and neurodegeneration: The molecular connection
-
Lee DW, Andersen JK, Kaur D. Iron dysregulation and neurodegeneration: the molecular connection. Mol Interv 2006;6:89-97.
-
(2006)
Mol Interv
, vol.6
, pp. 89-97
-
-
Lee, D.W.1
Andersen, J.K.2
Kaur, D.3
-
16
-
-
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, 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
-
17
-
-
0027102161
-
Diseases associated with calcium pyrophosphate deposition disease
-
Jones AC, Chuck AJ, Arie EA, Green DJ, Doherty M. Diseases associated with calcium pyrophosphate deposition disease. Semin Arthritis Rheum 1992;22:188-202.
-
(1992)
Semin Arthritis Rheum
, vol.22
, pp. 188-202
-
-
Jones, A.C.1
Chuck, A.J.2
Arie, E.A.3
Green, D.J.4
Doherty, M.5
-
18
-
-
0030631265
-
Radiological features of the visceral and skeletal involvement of hemochromatosis
-
Jager HJ, Mehring U, Gotz GF, Neise M, Erlemann R, Kapp HJ, et al. Radiological features of the visceral and skeletal involvement of hemochromatosis. Eur Radiol 1997;7:1199-1206.
-
(1997)
Eur Radiol
, vol.7
, pp. 1199-1206
-
-
Jager, H.J.1
Mehring, U.2
Gotz, G.F.3
Neise, M.4
Erlemann, R.5
Kapp, H.J.6
-
19
-
-
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
-
20
-
-
1842579593
-
Hemochromatosis mutations in the general popularion: Iron overload progression rate
-
Andersen RV, Tybjaerg-Hansen A, Appleyard M, Birgens H, Nordestgaard BG. Hemochromatosis mutations in the general popularion: iron overload progression rate. Blood 2004;103:2914-2919.
-
(2004)
Blood
, vol.103
, pp. 2914-2919
-
-
Andersen, R.V.1
Tybjaerg-Hansen, A.2
Appleyard, M.3
Birgens, H.4
Nordestgaard, B.G.5
-
21
-
-
1442357145
-
Factor V Leiden and the risk for venous thromboembolism in the adult Danish population
-
Juul K, Tybjaerg-Hansen A, Schnohr P, Nordestgaard BG. Factor V Leiden and the risk for venous thromboembolism in the adult Danish population. Ann Intern Med 2004;140:330-337.
-
(2004)
Ann Intern Med
, vol.140
, pp. 330-337
-
-
Juul, K.1
Tybjaerg-Hansen, A.2
Schnohr, P.3
Nordestgaard, B.G.4
-
22
-
-
11144229240
-
Phenotype of heterozygotes for low-density lipoprotein receptor mutations identified in different background populations
-
Tybjaerg-Hansen A, Jensen HK, Benn M, Steffensen R, Jensen G, Nordestgaard BG. Phenotype of heterozygotes for low-density lipoprotein receptor mutations identified in different background populations. Arterioscler Thromb Vasc Biol 2005;25:211-215.
-
(2005)
Arterioscler Thromb Vasc Biol
, vol.25
, pp. 211-215
-
-
Tybjaerg-Hansen, A.1
Jensen, H.K.2
Benn, M.3
Steffensen, R.4
Jensen, G.5
Nordestgaard, B.G.6
-
23
-
-
20244372858
-
Hemochromatosis and iron-overload screening in a racially diverse population
-
Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, et al. Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med 2005;352:1769-1778.
-
(2005)
N Engl J Med
, vol.352
, pp. 1769-1778
-
-
Adams, P.C.1
Reboussin, D.M.2
Barton, J.C.3
McLaren, C.E.4
Eckfeldt, J.H.5
McLaren, G.D.6
-
24
-
-
1942436221
-
Mendelian randomization: Prospects, potentials, and limitations
-
Smith GD, Ebrahim S. Mendelian randomization: prospects, potentials, and limitations. Int J Epidemiol 2004;33:30-42.
-
(2004)
Int J Epidemiol
, vol.33
, pp. 30-42
-
-
Smith, G.D.1
Ebrahim, S.2
-
25
-
-
0037701646
-
Typical type 2 diabetes mellitus and HFE gene mutations: A population-based case-control study
-
Halsall DJ, McFarlane I, Luan J, Cox TM, Wareham NJ. Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case-control study. Hum Mol Genet 2003;12:1361-1365.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1361-1365
-
-
Halsall, D.J.1
McFarlane, I.2
Luan, J.3
Cox, T.M.4
Wareham, N.J.5
-
26
-
-
33644701629
-
HFE genetic variability, body iron stores, and the risk of type 2 diabetes in U.S. women
-
Qi L, Meigs J, Manson JE, Ma J, Hunter D, Rifai N, et al. HFE genetic variability, body iron stores, and the risk of type 2 diabetes in U.S. women. Diabetes 2005;54:3567-3572.
-
(2005)
Diabetes
, vol.54
, pp. 3567-3572
-
-
Qi, L.1
Meigs, J.2
Manson, J.E.3
Ma, J.4
Hunter, D.5
Rifai, N.6
-
27
-
-
33748691224
-
HFE mutations and risk of coronary heart disease in middle-aged women
-
van der A DL, Peeters PH, Grobbee DE, Roest M, Marx JJ, Voorbij HM, et al. HFE mutations and risk of coronary heart disease in middle-aged women. Eur J Clin Invest 2006;36:682-690.
-
(2006)
Eur J Clin Invest
, vol.36
, pp. 682-690
-
-
van der, A.D.1
Peeters, P.H.2
Grobbee, D.E.3
Roest, M.4
Marx, J.J.5
Voorbij, H.M.6
-
28
-
-
33747179546
-
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impaitment in a Portuguese cohort
-
Guerreiro RJ, Bras JM, Santana I, Januario C, Santiago B, Morgadinho AS, et al. Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impaitment in a Portuguese cohort. BMC Neurol 2006;6:24.
-
(2006)
BMC Neurol
, vol.6
, pp. 24
-
-
Guerreiro, R.J.1
Bras, J.M.2
Santana, I.3
Januario, C.4
Santiago, B.5
Morgadinho, A.S.6
-
29
-
-
0036834414
-
The role of hemochromatosis C282Y and H63D gene mutations in type 2 diabetes: Findings from the Rotterdam study and meta-analysis
-
Njajou OT, Alizadeh BZ, Vaessen N, Vergeer J, Houwing-Duistermaat J, Hofman A, et al. The role of hemochromatosis C282Y and H63D gene mutations in type 2 diabetes: findings from the Rotterdam study and meta-analysis. Diabetes Care 2002;25:2112-2113.
-
(2002)
Diabetes Care
, vol.25
, pp. 2112-2113
-
-
Njajou, O.T.1
Alizadeh, B.Z.2
Vaessen, N.3
Vergeer, J.4
Houwing-Duistermaat, J.5
Hofman, A.6
-
30
-
-
0034685429
-
Meta-analysis of observational studies in epidemiology: A proposal for reporting
-
for the Meta-Analysis of Observational Studies in Epidemiology Group
-
Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al., for the Meta-Analysis of Observational Studies in Epidemiology Group. Meta-analysis of observational studies in epidemiology: a proposal for reporting. JAMA 2000;283:2008-2012.
-
(2000)
JAMA
, vol.283
, pp. 2008-2012
-
-
Stroup, D.F.1
Berlin, J.A.2
Morton, S.C.3
Olkin, I.4
Williamson, G.D.5
Rennie, D.6
|