-
2
-
-
33745908863
-
Iron binding dendrimers: A novel approach for the treatment of haemochromatosis
-
Zhou T, Neubert H, Liu DY, Liu ZD, Ma YM, Kong XL, Luo W, Mark S, Hider RC. Iron binding dendrimers: a novel approach for the treatment of haemochromatosis. J Med Chem 2006;49:4171-4182
-
(2006)
J Med Chem
, vol.49
, pp. 4171-4182
-
-
Zhou, T.1
Neubert, H.2
Liu, D.Y.3
Liu, Z.D.4
Ma, Y.M.5
Kong, X.L.6
Luo, W.7
Mark, S.8
Hider, R.C.9
-
3
-
-
0029913626
-
Long-term survival in patients with hereditary hemochromatosis
-
Niederau C, Fischer R, Purschel A, Stremmel W, Haussinger D, Strohmeyer G. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology 1996;110:1107-1119
-
(1996)
Gastroenterology
, vol.110
, pp. 1107-1119
-
-
Niederau, C.1
Fischer, R.2
Purschel, A.3
Stremmel, W.4
Haussinger, D.5
Strohmeyer, G.6
-
4
-
-
0028366852
-
Preventing manifestations of hereditary haemochromatosis through population based screening
-
Haddow JE, Ledue TB. Preventing manifestations of hereditary haemochromatosis through population based screening. J Med Screen 1994;1:16-21.
-
(1994)
J Med Screen
, vol.1
, pp. 16-21
-
-
Haddow, J.E.1
Ledue, T.B.2
-
5
-
-
17944369464
-
Screening for hemochromatosis: High prevalence and low morbidity in an unselected population of 65,238 persons
-
Å sberg A, Hveem K, Thorstensen K, Ellekjær E, Kannelønning K, Fjøsne U, Halvorsen TB, Smethurst HB, Sagen E, Bjerve KS. 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
-
-
Åsberg, A.1
Hveem, K.2
Thorstensen, K.3
Ellekjær, E.4
Kannelønning, K.5
Fjøsne, U.6
Halvorsen, T.B.7
Smethurst, H.B.8
Sagen, E.9
Bjerve, K.S.10
-
6
-
-
0036016994
-
Hereditary hemochromatosis: The clinical signifi cance of the S65C mutation
-
Åsberg A, Thorstensen K, Hveem K, Bjerve KS. Hereditary hemochromatosis: the clinical signifi cance of the S65C mutation. Genet Test 2002;6:59-62.
-
(2002)
Genet Test
, vol.6
, pp. 59-62
-
-
Åsberg, A.1
Thorstensen, K.2
Hveem, K.3
Bjerve, K.S.4
-
7
-
-
1542327893
-
The Nord-Trøndelag Health Study 1995-1997 (HUNT2): Objectives, contents, methods and participation
-
Holmen J, Midthjell K, Krüger Ø, Langhammer A, Holmen TL, Bratberg GH, Vatten L, Lund-Larsen PG. The Nord-Trøndelag Health Study 1995-1997 (HUNT2): objectives, contents, methods and participation. Norsk Epidemiologi 2003;13:19-32.
-
(2003)
Norsk Epidemiologi
, vol.13
, pp. 19-32
-
-
Holmen, J.1
Midthjell, K.2
Krüger Ø3
Langhammer, A.4
Holmen, T.L.5
Bratberg, G.H.6
Vatten, L.7
Lund-Larsen, P.G.8
-
8
-
-
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, Dormishian F, Domingo RJ, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Wolff RK. 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
Dormishian, F.7
Domingo, R.J.8
Ellis, M.C.9
Fullan, A.10
Hinton, L.M.11
Jones, N.L.12
Kimmel, B.E.13
Kronmal, G.S.14
Lauer, P.15
Lee, V.K.16
Loeb, D.B.17
Mapa, F.A.18
McClelland, E.19
Meyer, N.C.20
Mintier, G.A.21
Moeller, N.22
Moore, T.23
Morikang, E.24
Wolff, R.K.25
more..
-
9
-
-
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. Nat Genet 1999;22:325-326
-
(1999)
Nat Genet
, vol.22
, pp. 325-326
-
-
Jeffrey, G.P.1
Chakrabarti, S.2
Hegele Ra Adams, P.C.3
-
10
-
-
0032858222
-
Rapid genotyping of hemochromatosis gene mutations on the LightCycler with fl uorescent hybridization probes
-
Mangasser-Stephan K, Tag C, Reiser A, Gressner AM. Rapid genotyping of hemochromatosis gene mutations on the LightCycler with fl uorescent hybridization probes. Clin Chem 1999;45:1875-1878
-
(1999)
Clin Chem
, vol.45
, pp. 1875-1878
-
-
Mangasser-Stephan, K.1
Tag, C.2
Reiser, A.3
Gressner, A.M.4
-
11
-
-
0032712283
-
LightCycler PCR assay for simultaneous detection of the H63D and S65C mutations in the HFE hemochromatosis gene based on opposite melting temperature shifts
-
Bollhalder M, Mura C, Landt O, Maly FE. LightCycler PCR assay for simultaneous detection of the H63D and S65C mutations in the HFE hemochromatosis gene based on opposite melting temperature shifts. Clin Chem 1999; 45:2275-2278
-
(1999)
Clin Chem
, vol.45
, pp. 2275-2278
-
-
Bollhalder, M.1
Mura, C.2
Landt, O.3
Maly, F.E.4
-
13
-
-
0031040065
-
Prevalence of hemochromatosis among fi rst time and repeat blood donors in Norway
-
Bell H, Thordal C, Raknerud N, Hansen T, Bosnes V, Halvorsen R, Heier HE, Try K, Leivestad T, Thomassen Y. Prevalence of hemochromatosis among fi rst time and repeat blood donors in Norway. J Hepatol 1997;26:272-279
-
(1997)
J Hepatol
, vol.26
, pp. 272-279
-
-
Bell, H.1
Thordal, C.2
Raknerud, N.3
Hansen, T.4
Bosnes, V.5
Halvorsen, R.6
Heier, H.E.7
Try, K.8
Leivestad, T.9
Thomassen, Y.10
-
14
-
-
0032986271
-
High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression
-
Distante S, Berg JP, Lande K, Haug E, Bell H. High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression. Scand J Gastroenterol 1999;34:529-534
-
(1999)
Scand J Gastroenterol
, vol.34
, pp. 529-534
-
-
Distante, S.1
Berg, J.P.2
Lande, K.3
Haug, E.4
Bell, H.5
-
15
-
-
20244372858
-
Hemochromatosis and iron-overload screening in a racially diverse population
-
Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FD, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P. 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
Dawkins, F.D.7
Acton, R.T.8
Harris, E.L.9
Gordeuk, V.R.10
Leiendecker-Foster, C.11
Speechley, M.12
Snively, B.M.13
Holup, J.L.14
Thomson, E.15
Sholinsky, P.16
-
16
-
-
0034883430
-
HFE mutations, iron defi ciency and overload in 10 500 blood donors
-
Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M. HFE mutations, iron defi ciency and overload in 10 500 blood donors. Br J Haematol 2001;114:474-484
-
(2001)
Br J Haematol
, vol.114
, pp. 474-484
-
-
Jackson, H.A.1
Carter, K.2
Darke, C.3
Guttridge, M.G.4
Ravine, D.5
Hutton, R.D.6
Napier, J.A.7
Worwood, M.8
-
17
-
-
0033517343
-
A population-based study of the clinical expression of the hemochromatosis gene
-
Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell L. 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.6
-
18
-
-
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, Haug E, Bell H. 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
Haug, E.4
Bell, H.5
-
20
-
-
38349079861
-
Iron-overload-related disease in HFE hereditary hemochromatosis
-
Allen JK, Gurrin LC, Constantine CC, Osborne NJ, Delatycki MB, Nicoll AJ, McLaren CE, Bahlo M, Nisselle AE, Vulpe CD, Anderson GJ, Southey MC, Giles GG, English DR, Hopper JL, Olynyk JK, Powell LW, Gertig DM. Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med 2008;358:221-230 .
-
(2008)
N Engl J Med
, vol.358
, pp. 221-230
-
-
Allen, J.K.1
Gurrin, L.C.2
Constantine, C.C.3
Osborne, N.J.4
Delatycki, M.B.5
Nicoll, A.J.6
McLaren, C.E.7
Bahlo, M.8
Nisselle, A.E.9
Vulpe, C.D.10
Anderson, G.J.11
Southey, M.C.12
Giles, G.G.13
English, D.R.14
Hopper, J.L.15
Olynyk, J.K.16
Powell, L.W.17
Gertig, D.M.18
|