-
1
-
-
0036209551
-
-
Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis
-
Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis. Braz J Med Biol Res. 2002;35(3):329-35.
-
(2002)
Braz J Med Biol Res
, vol.35
, Issue.3
, pp. 329-335
-
-
-
2
-
-
3042542834
-
Hereditary haemochromatosis
-
Limdi JK, Crampton JR. Hereditary haemochromatosis. QJM. 2004;97(6):315-24.
-
(2004)
QJM
, vol.97
, Issue.6
, pp. 315-324
-
-
Limdi, J.K.1
Crampton, J.R.2
-
3
-
-
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(23):2383-97
-
(2004)
N Engl J Med
, vol.350
, Issue.23
, pp. 2383-2397
-
-
Pietrangelo, A.1
-
4
-
-
30344479814
-
S65C and other mutations in the haemochromatosis gene in the Czech population
-
Cimburová M, Putová I, Provazníkova H, et al. S65C and other mutations in the haemochromatosis gene in the Czech population. Folia Biol (Praha). 2005;51(6): 172-6.
-
(2005)
Folia Biol (Praha)
, vol.51
, Issue.6
, pp. 172-176
-
-
Cimburová, M.1
Putová, I.2
Provazníkova, H.3
-
5
-
-
26444490676
-
Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: New epidemiological data
-
Scotet V, Le Gac G, Mérour MC, et al. Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data. BMC Medical Genetics 2005;6:24.
-
(2005)
BMC Medical Genetics
, vol.6
, pp. 24
-
-
Scotet, V.1
Le Gac, G.2
Mérour, M.C.3
-
6
-
-
33746802494
-
-
US. Preventive Services Task Force. Screening for hemochromatosis: recommendation statement. Ann Intern Med. 2006; 145(3):204-8.
-
US. Preventive Services Task Force. Screening for hemochromatosis: recommendation statement. Ann Intern Med. 2006; 145(3):204-8.
-
-
-
-
7
-
-
0344082047
-
Population genetic screening for hereditary haemochromatosis
-
Gertig DM, Hopper JL, Allen KJ. Population genetic screening for hereditary haemochromatosis. Med J Aust. 2003; 179(10):517-8.
-
(2003)
Med J Aust
, vol.179
, Issue.10
, pp. 517-518
-
-
Gertig, D.M.1
Hopper, J.L.2
Allen, K.J.3
-
8
-
-
20944451697
-
Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000)
-
Martinelli AL, Filho R, Cruz S, et al. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000). Genet Mol Res. 2005;4(1):31-8.
-
(2005)
Genet Mol Res
, vol.4
, Issue.1
, pp. 31-38
-
-
Martinelli, A.L.1
Filho, R.2
Cruz, S.3
-
9
-
-
33747179546
-
Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort
-
Guerreiro RJ, Bras JM, Santana I, et al. Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort. BMC Neurology. 2006;6:24.
-
(2006)
BMC Neurology
, vol.6
, pp. 24
-
-
Guerreiro, R.J.1
Bras, J.M.2
Santana, I.3
-
10
-
-
58049160047
-
-
Hemochromatosis. Em: Online Mendelian Inheritance in Man, OMIM. (Accessed April 02, 2007, em http://www.ncbi.nlm.nih.gov/omim/.)
-
Hemochromatosis. Em: Online Mendelian Inheritance in Man, OMIM. (Accessed April 02, 2007, em http://www.ncbi.nlm.nih.gov/omim/.)
-
-
-
-
11
-
-
33847656226
-
HFE gene mutations in Brazilian thalassemic patients
-
Oliveira TM, Souza FP, Jardim AC, et al. HFE gene mutations in Brazilian thalassemic patients. Braz J Med Biol Res. 2006;39 (12):1575-80
-
(2006)
Braz J Med Biol Res
, vol.39
, Issue.12
, pp. 1575-1580
-
-
Oliveira, T.M.1
Souza, F.P.2
Jardim, A.C.3
-
12
-
-
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(9302):211-8.
-
(2002)
Lancet
, vol.359
, Issue.9302
, pp. 211-218
-
-
Beutler, E.1
Felitti, V.J.2
Koziol, J.A.3
Ho, N.J.4
Gelbart, T.5
-
13
-
-
58049134265
-
Hereditary hemocrhomatosis and HFE gene mutations
-
Domingos CRB. Hereditary hemocrhomatosis and HFE gene mutations. Rev Bras Hematol e Hemoter. 2006;28(4):239-45.
-
(2006)
Rev Bras Hematol e Hemoter
, vol.28
, Issue.4
, pp. 239-245
-
-
Domingos, C.R.B.1
-
14
-
-
33144456592
-
Hemochromatosis: Genetics and pathophysiology
-
Beutler E. Hemochromatosis: genetics and pathophysiology. Annu Rev Med. 2006;57:331-47.
-
(2006)
Annu Rev Med
, vol.57
, pp. 331-347
-
-
Beutler, E.1
-
15
-
-
0034146770
-
HFE gene mutations in coronary atherothrombotic disease
-
Calado RT, Franco RF, Pazin-Filho A, et al. HFE gene mutations in coronary atherothrombotic disease. Braz J Med Biol Res. 2000; 33(3):301-6
-
(2000)
Braz J Med Biol Res
, vol.33
, Issue.3
, pp. 301-306
-
-
Calado, R.T.1
Franco, R.F.2
Pazin-Filho, A.3
-
16
-
-
58049141009
-
-
Raymond M. & Rousset F. GENEPOP, version 1.2: population genetics software for exact tests and ecumenicism. J. Heredity 1995;86:248-24916
-
Raymond M. & Rousset F. GENEPOP, version 1.2: population genetics software for exact tests and ecumenicism. J. Heredity 1995;86:248-24916.
-
-
-
-
17
-
-
1842579593
-
Hemochromatosis mutations in the general population: Iron overload progression rate
-
Andersen RV, Tybjaerg-Hansen A, Appleyard M, et al. Hemochromatosis mutations in the general population: iron overload progression rate. Blood. 2004;103(8):2914-9.
-
(2004)
Blood
, vol.103
, Issue.8
, pp. 2914-2919
-
-
Andersen, R.V.1
Tybjaerg-Hansen, A.2
Appleyard, M.3
-
18
-
-
58049135487
-
Genética Molecular Humana
-
Artmed, Porto Alegre
-
aed, Artmed, Porto Alegre 2001; pp. 64-66.
-
(2001)
aed
, pp. 64-66
-
-
Strachan, T.1
Read, A.P.2
-
19
-
-
0033380773
-
Mutation analysis of the HFE gene in Brazilian populations
-
Agostinho MF, Arruda VR, Basseres DS, et al Mutation analysis of the HFE gene in Brazilian populations. Blood Cells Mol Dis. 1999;25(5-6):324-7.
-
(1999)
Blood Cells Mol Dis
, vol.25
, Issue.5-6
, pp. 324-327
-
-
Agostinho, M.F.1
Arruda, V.R.2
Basseres, D.S.3
-
20
-
-
0033369104
-
Are haemochromatosis mutations related to the severity of liver disease in hepatitis C virus infection?
-
Martinelli AL, Franco RF, Villanova MG, et al. Are haemochromatosis mutations related to the severity of liver disease in hepatitis C virus infection? Acta Haematol. 2000; 102(3): 152-6.
-
(2000)
Acta Haematol
, vol.102
, Issue.3
, pp. 152-156
-
-
Martinelli, A.L.1
Franco, R.F.2
Villanova, M.G.3
-
22
-
-
24744448067
-
Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients
-
Perícole FV, Alves MA, Saad ST, Costa FF. Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients. Braz J Med Biol Res. 2005;38(9):1321-4.
-
(2005)
Braz J Med Biol Res
, vol.38
, Issue.9
, pp. 1321-1324
-
-
Perícole, F.V.1
Alves, M.A.2
Saad, S.T.3
Costa, F.F.4
-
23
-
-
33845298021
-
Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study
-
Acton RT, Barton JC, Passmore LV, et al. Relationships of serum ferritin, transferrin saturation, and HFE mutations and self-reported diabetes in the Hemochromatosis and Iron Overload Screening (HEIRS) study. Diabetes Care. 2006;29(9):2084-9.
-
(2006)
Diabetes Care
, vol.29
, Issue.9
, pp. 2084-2089
-
-
Acton, R.T.1
Barton, J.C.2
Passmore, L.V.3
|