-
5
-
-
0017158302
-
Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis
-
Simon M., Bourel M., Fauchet R., and Genetet B. Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis. Gut 17 (1976) 332-334
-
(1976)
Gut
, vol.17
, pp. 332-334
-
-
Simon, M.1
Bourel, M.2
Fauchet, R.3
Genetet, B.4
-
6
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder J.N., Gnirke A., Thomas W., Tsuchihashi Z., Ruddy D.A., Basava A., et al. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet 13 (1996) 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
-
7
-
-
0035353167
-
New mutations inactivating transferrin receptor 2 in hemochromatosis type 3
-
Roetto A., Totaro A., Piperno A., Piga A., Longo F., Garozzo G., et al. New mutations inactivating transferrin receptor 2 in hemochromatosis type 3. Blood 97 (2001) 2555-2560
-
(2001)
Blood
, vol.97
, pp. 2555-2560
-
-
Roetto, A.1
Totaro, A.2
Piperno, A.3
Piga, A.4
Longo, F.5
Garozzo, G.6
-
8
-
-
20244388240
-
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis
-
Roetto A., Papanikolaou G., Politou M., Alberti F., Girelli D., Christakis J., et al. Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis. Nat Genet 33 (2003) 21-22
-
(2003)
Nat Genet
, vol.33
, pp. 21-22
-
-
Roetto, A.1
Papanikolaou, G.2
Politou, M.3
Alberti, F.4
Girelli, D.5
Christakis, J.6
-
9
-
-
9144252017
-
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis
-
Papanikolaou G., Samuels M.E., Ludwig E.H., MacDonald M.L., Franchini P.L., Dube M.P., et al. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis. Nat Genet 36 (2004) 77-82
-
(2004)
Nat Genet
, vol.36
, pp. 77-82
-
-
Papanikolaou, G.1
Samuels, M.E.2
Ludwig, E.H.3
MacDonald, M.L.4
Franchini, P.L.5
Dube, M.P.6
-
10
-
-
17944380796
-
Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene
-
Montosi G., Donovan A., Totaro A., Garuti C., Pignatti E., Cassanelli S., et al. Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene. J Clin Invest 108 (2001) 619-623
-
(2001)
J Clin Invest
, vol.108
, pp. 619-623
-
-
Montosi, G.1
Donovan, A.2
Totaro, A.3
Garuti, C.4
Pignatti, E.5
Cassanelli, S.6
-
11
-
-
0034930197
-
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
-
Njajou O.T., Vaessen N., Joosse M., Berghuis B., van Dongen J.W., Breuning M.H., et al. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis. Nat Genet 28 (2001) 213-214
-
(2001)
Nat Genet
, vol.28
, pp. 213-214
-
-
Njajou, O.T.1
Vaessen, N.2
Joosse, M.3
Berghuis, B.4
van Dongen, J.W.5
Breuning, M.H.6
-
12
-
-
0035896581
-
A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload
-
Pigeon C., Ilyin G., Courselaud B., Leroyer P., Turlin B., Brissot P., et al. A new mouse liver-specific gene, encoding a protein homologous to human antimicrobial peptide hepcidin, is overexpressed during iron overload. J Biol Chem 276 (2001) 7811-7819
-
(2001)
J Biol Chem
, vol.276
, pp. 7811-7819
-
-
Pigeon, C.1
Ilyin, G.2
Courselaud, B.3
Leroyer, P.4
Turlin, B.5
Brissot, P.6
-
13
-
-
0035902605
-
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice
-
Nicolas G., Bennoun M., Devaux I., Beaumont C., Grandchamp B., Kahn A., et al. Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice. Proc Natl Acad Sci U S A 98 (2001) 8780-8785
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 8780-8785
-
-
Nicolas, G.1
Bennoun, M.2
Devaux, I.3
Beaumont, C.4
Grandchamp, B.5
Kahn, A.6
-
14
-
-
10844258104
-
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
-
Nemeth E., Tuttle M.S., Powelson J., Vaughn M.B., Donovan A., Ward D.M., et al. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 306 (2004) 2090-2093
-
(2004)
Science
, vol.306
, pp. 2090-2093
-
-
Nemeth, E.1
Tuttle, M.S.2
Powelson, J.3
Vaughn, M.B.4
Donovan, A.5
Ward, D.M.6
-
15
-
-
48149090865
-
The hepcidin-binding site on ferroportin is evolutionarily conserved
-
De Domenico I., Nemeth E., Nelson J.M., Phillips J.D., Ajioka R.S., Kay M.S., et al. The hepcidin-binding site on ferroportin is evolutionarily conserved. Cell Metab 8 (2008) 146-156
-
(2008)
Cell Metab
, vol.8
, pp. 146-156
-
-
De Domenico, I.1
Nemeth, E.2
Nelson, J.M.3
Phillips, J.D.4
Ajioka, R.S.5
Kay, M.S.6
-
16
-
-
70249115636
-
-
Brissot P, Le Lan C, Troadec MB, Ropert M, Gaboriau F, Lescoat G, et al. Diagnosis and treatment of HFE-haemochromatosis. In: Handbook ESoH, ed. Disorders of iron homeostasis, Erythrocytes, Erythropoiesis (in press).
-
Brissot P, Le Lan C, Troadec MB, Ropert M, Gaboriau F, Lescoat G, et al. Diagnosis and treatment of HFE-haemochromatosis. In: Handbook ESoH, ed. Disorders of iron homeostasis, Erythrocytes, Erythropoiesis (in press).
-
-
-
-
17
-
-
43949090838
-
Current approach to hemochromatosis
-
Brissot P., Troadec M.B., Bardou-Jacquet E., Lan C.L., Jouanolle A.M., Deugnier Y., et al. Current approach to hemochromatosis. Blood Rev 22 (2008) 195-210
-
(2008)
Blood Rev
, vol.22
, pp. 195-210
-
-
Brissot, P.1
Troadec, M.B.2
Bardou-Jacquet, E.3
Lan, C.L.4
Jouanolle, A.M.5
Deugnier, Y.6
-
18
-
-
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 350 (2004) 2383-2397
-
(2004)
N Engl J Med
, vol.350
, pp. 2383-2397
-
-
Pietrangelo, A.1
-
19
-
-
0037132786
-
Penetrance of 845G: A (C282Y) HFE hereditary haemochromatosis mutation in the USA
-
Beutler E., Felitti V.J., Koziol J.A., Ho N.J., and Gelbart T. Penetrance of 845G: A (C282Y) HFE hereditary haemochromatosis mutation in the USA. Lancet 359 (2002) 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
-
-
38349079861
-
Iron-overload-related disease in HFE hereditary hemochromatosis
-
Allen K.J., Gurrin L.C., Constantine C.C., Osborne N.J., Delatycki M.B., Nicoll A.J., et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med 358 (2008) 221-230
-
(2008)
N Engl J Med
, vol.358
, pp. 221-230
-
-
Allen, K.J.1
Gurrin, L.C.2
Constantine, C.C.3
Osborne, N.J.4
Delatycki, M.B.5
Nicoll, A.J.6
-
21
-
-
70249126586
-
French recommendations for management of HFE hemochromatosis
-
HAS,
-
HAS. French recommendations for management of HFE hemochromatosis. Haute Autorité de santé 2005 : www.has-sante.fr.
-
(2005)
Haute Autorité de santé
-
-
-
22
-
-
0034022636
-
The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22
-
Camaschella C., Roetto A., Cali A., De Gobbi M., Garozzo G., Carella M., et al. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. Nat Genet 25 (2000) 14-15
-
(2000)
Nat Genet
, vol.25
, pp. 14-15
-
-
Camaschella, C.1
Roetto, A.2
Cali, A.3
De Gobbi, M.4
Garozzo, G.5
Carella, M.6
-
23
-
-
0037354313
-
Aceruloplasminemia, an inherited disorder of iron metabolism
-
Miyajima H., Takahashi Y., and Kono S. Aceruloplasminemia, an inherited disorder of iron metabolism. Biometals 16 (2003) 205-213
-
(2003)
Biometals
, vol.16
, pp. 205-213
-
-
Miyajima, H.1
Takahashi, Y.2
Kono, S.3
-
24
-
-
33745761771
-
Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia
-
Kono S., Suzuki H., Takahashi K., Takahashi Y., Shirakawa K., Murakawa Y., et al. Hepatic iron overload associated with a decreased serum ceruloplasmin level in a novel clinical type of aceruloplasminemia. Gastroenterology 131 (2006) 240-245
-
(2006)
Gastroenterology
, vol.131
, pp. 240-245
-
-
Kono, S.1
Suzuki, H.2
Takahashi, K.3
Takahashi, Y.4
Shirakawa, K.5
Murakawa, Y.6
-
25
-
-
33646370235
-
Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression
-
Babitt J.L., Huang F.W., Wrighting D.M., Xia Y., Sidis Y., Samad T.A., et al. Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression. Nat Genet 38 (2006) 531-539
-
(2006)
Nat Genet
, vol.38
, pp. 531-539
-
-
Babitt, J.L.1
Huang, F.W.2
Wrighting, D.M.3
Xia, Y.4
Sidis, Y.5
Samad, T.A.6
-
26
-
-
33644876815
-
A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression
-
Wang R., Li C., Xu X., Zheng Y., Xiao C., Zerfas P., et al. A role of SMAD4 in iron metabolism through the positive regulation of hepcidin expression. Cell Metab 2 (2005) 399-409
-
(2005)
Cell Metab
, vol.2
, pp. 399-409
-
-
Wang, R.1
Li, C.2
Xu, X.3
Zheng, Y.4
Xiao, C.5
Zerfas, P.6
-
27
-
-
47649126246
-
Forging a field: the golden age of iron biology
-
Andrews N.C. Forging a field: the golden age of iron biology. Blood 112 (2008) 219-230
-
(2008)
Blood
, vol.112
, pp. 219-230
-
-
Andrews, N.C.1
-
28
-
-
38649128515
-
HFE acts in hepatocytes to prevent hemochromatosis
-
Vujic Spasic M., Kiss J., Herrmann T., Galy B., Martinache S., Stolte J., et al. HFE acts in hepatocytes to prevent hemochromatosis. Cell Metab 7 (2008) 173-178
-
(2008)
Cell Metab
, vol.7
, pp. 173-178
-
-
Vujic Spasic, M.1
Kiss, J.2
Herrmann, T.3
Galy, B.4
Martinache, S.5
Stolte, J.6
-
29
-
-
34250800318
-
Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin
-
De Domenico I., Ward D.M., di Patti M.C., Jeong S.Y., David S., Musci G., et al. Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI-ceruloplasmin. EMBO J 26 (2007) 2823-2831
-
(2007)
EMBO J
, vol.26
, pp. 2823-2831
-
-
De Domenico, I.1
Ward, D.M.2
di Patti, M.C.3
Jeong, S.Y.4
David, S.5
Musci, G.6
-
30
-
-
0018164919
-
Non-specific serum iron in thalassaemia: an abnormal serum iron fraction of potential toxicity
-
Hershko C., Graham G., Bates G.W., and Rachmilewitz E.A. Non-specific serum iron in thalassaemia: an abnormal serum iron fraction of potential toxicity. Br J Haematol 40 (1978) 255-263
-
(1978)
Br J Haematol
, vol.40
, pp. 255-263
-
-
Hershko, C.1
Graham, G.2
Bates, G.W.3
Rachmilewitz, E.A.4
-
31
-
-
17944388628
-
Nature of nontransferrin-bound iron
-
Hider R.C. Nature of nontransferrin-bound iron. Eur J Clin Invest 32 Suppl 1 (2002) 50-54
-
(2002)
Eur J Clin Invest
, vol.32
, Issue.SUPPL. 1
, pp. 50-54
-
-
Hider, R.C.1
-
32
-
-
0141705304
-
Labile plasma iron in iron overload: redox activity and susceptibility to chelation
-
Esposito B.P., Breuer W., Sirankapracha P., Pootrakul P., Hershko C., and Cabantchik Z.I. Labile plasma iron in iron overload: redox activity and susceptibility to chelation. Blood 102 (2003) 2670-2677
-
(2003)
Blood
, vol.102
, pp. 2670-2677
-
-
Esposito, B.P.1
Breuer, W.2
Sirankapracha, P.3
Pootrakul, P.4
Hershko, C.5
Cabantchik, Z.I.6
-
33
-
-
21144441802
-
Redox active plasma iron in C282Y/C282Y hemochromatosis
-
Le Lan C., Loreal O., Cohen T., Ropert M., Glickstein H., Laine F., et al. Redox active plasma iron in C282Y/C282Y hemochromatosis. Blood 105 (2005) 4527-4531
-
(2005)
Blood
, vol.105
, pp. 4527-4531
-
-
Le Lan, C.1
Loreal, O.2
Cohen, T.3
Ropert, M.4
Glickstein, H.5
Laine, F.6
-
34
-
-
0022345593
-
Efficient clearance of non-transferrin-bound iron by rat liver. Implications for hepatic iron loading in iron overload states
-
Brissot P., Wright T.L., Ma W.L., and Weisiger R.A. Efficient clearance of non-transferrin-bound iron by rat liver. Implications for hepatic iron loading in iron overload states. J Clin Invest 76 (1985) 1463-1470
-
(1985)
J Clin Invest
, vol.76
, pp. 1463-1470
-
-
Brissot, P.1
Wright, T.L.2
Ma, W.L.3
Weisiger, R.A.4
-
35
-
-
43949115966
-
Non-invasive assessment of hepatic iron stores by MRI
-
Gandon Y., Olivié D., Guyader D., Aubé C., Oberti F., Sebille V., et al. Non-invasive assessment of hepatic iron stores by MRI. Lancet 33 (2004) 338-343
-
(2004)
Lancet
, vol.33
, pp. 338-343
-
-
Gandon, Y.1
Olivié, D.2
Guyader, D.3
Aubé, C.4
Oberti, F.5
Sebille, V.6
-
36
-
-
11244355277
-
Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance
-
St Pierre T.G., Clark P.R., Chua-anusorn W., Fleming A.J., Jeffrey G.P., Olynyk J.K., et al. Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance. Blood 105 (2005) 855-861
-
(2005)
Blood
, vol.105
, pp. 855-861
-
-
St Pierre, T.G.1
Clark, P.R.2
Chua-anusorn, W.3
Fleming, A.J.4
Jeffrey, G.P.5
Olynyk, J.K.6
-
37
-
-
19544369489
-
Molecular characterization of a third case of human atransferrinemia
-
Knisely A.S., Gelbart T., and Beutler E. Molecular characterization of a third case of human atransferrinemia. Blood 104 (2004) 2607
-
(2004)
Blood
, vol.104
, pp. 2607
-
-
Knisely, A.S.1
Gelbart, T.2
Beutler, E.3
-
38
-
-
12844260664
-
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload
-
Mims M.P., Guan Y., Pospisilova D., Priwitzerova M., Indrak K., Ponka P., et al. Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload. Blood 105 (2005) 1337-1342
-
(2005)
Blood
, vol.105
, pp. 1337-1342
-
-
Mims, M.P.1
Guan, Y.2
Pospisilova, D.3
Priwitzerova, M.4
Indrak, K.5
Ponka, P.6
-
39
-
-
33646537173
-
Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload
-
Beaumont C., Delaunay J., Hetet G., Grandchamp B., de Montalembert M., and Tchernia G. Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload. Blood 107 (2006) 4168-4170
-
(2006)
Blood
, vol.107
, pp. 4168-4170
-
-
Beaumont, C.1
Delaunay, J.2
Hetet, G.3
Grandchamp, B.4
de Montalembert, M.5
Tchernia, G.6
-
40
-
-
30144443274
-
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)
-
Iolascon A., d'Apolito M., Servedio V., Cimmino F., Piga A., and Camaschella C. Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2). Blood 107 (2006) 349-354
-
(2006)
Blood
, vol.107
, pp. 349-354
-
-
Iolascon, A.1
d'Apolito, M.2
Servedio, V.3
Cimmino, F.4
Piga, A.5
Camaschella, C.6
-
41
-
-
34548013116
-
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
-
Camaschella C., Campanella A., De Falco L., Boschetto L., Merlini R., Silvestri L., et al. The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. Blood 110 (2007) 1353-1358
-
(2007)
Blood
, vol.110
, pp. 1353-1358
-
-
Camaschella, C.1
Campanella, A.2
De Falco, L.3
Boschetto, L.4
Merlini, R.5
Silvestri, L.6
-
43
-
-
41549127253
-
Iron homeostasis: fitting the puzzle pieces together
-
Ganz T. Iron homeostasis: fitting the puzzle pieces together. Cell Metab 7 (2008) 288-290
-
(2008)
Cell Metab
, vol.7
, pp. 288-290
-
-
Ganz, T.1
-
44
-
-
1642367900
-
HAMP as a modifier gene that increase the phenotypic expression of the HFE C282Y homozygous genotype
-
Jacolot S., Le Gac G., Scotet V., Quere I., Mura C., and Ferec C. HAMP as a modifier gene that increase the phenotypic expression of the HFE C282Y homozygous genotype. Blood 103 (2004) 2835-2840
-
(2004)
Blood
, vol.103
, pp. 2835-2840
-
-
Jacolot, S.1
Le Gac, G.2
Scotet, V.3
Quere, I.4
Mura, C.5
Ferec, C.6
-
45
-
-
10744225120
-
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis
-
Merryweather-Clarke A.T., Cadet E., Bomford A., Capron D., Viprakasit V., Miller A., et al. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis. Hum Mol Genet 12 (2003) 2241-2247
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2241-2247
-
-
Merryweather-Clarke, A.T.1
Cadet, E.2
Bomford, A.3
Capron, D.4
Viprakasit, V.5
Miller, A.6
-
46
-
-
4544314123
-
The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype
-
Le Gac G., Scotet V., Ka C., Gourlaouen I., Bryckaert L., Jacolot S., et al. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype. Hum Mol Genet 13 (2004) 1913-1918
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1913-1918
-
-
Le Gac, G.1
Scotet, V.2
Ka, C.3
Gourlaouen, I.4
Bryckaert, L.5
Jacolot, S.6
-
47
-
-
35349002878
-
Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway module HFE hemochromatosis penetrance
-
Millet J., Dehais V., Bourgain C., Jouanolle A.M., Mosser A., Perrin M., et al. Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway module HFE hemochromatosis penetrance. Am J Hum Genet 81 (2007) 799-807
-
(2007)
Am J Hum Genet
, vol.81
, pp. 799-807
-
-
Millet, J.1
Dehais, V.2
Bourgain, C.3
Jouanolle, A.M.4
Mosser, A.5
Perrin, M.6
-
48
-
-
57249103568
-
The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis
-
Gurrin L.C., Osborne N.J., Constantine C.C., McLaren C.E., English D.R., Gertig D.M., et al. The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis. Gastroenterology 135 (2008) 1945-1952
-
(2008)
Gastroenterology
, vol.135
, pp. 1945-1952
-
-
Gurrin, L.C.1
Osborne, N.J.2
Constantine, C.C.3
McLaren, C.E.4
English, D.R.5
Gertig, D.M.6
-
49
-
-
54949147441
-
Immunoassay for human serum hepcidin
-
Ganz T., Olbina G., Girelli D., Nemeth E., and Westerman M. Immunoassay for human serum hepcidin. Blood 112 (2008) 4292-4297
-
(2008)
Blood
, vol.112
, pp. 4292-4297
-
-
Ganz, T.1
Olbina, G.2
Girelli, D.3
Nemeth, E.4
Westerman, M.5
-
50
-
-
53249121484
-
Hepcidin in the management of patients with mild non-hemochromatotic iron overload: fact or fiction?
-
Swinkels D.W., and Drenth J.P. Hepcidin in the management of patients with mild non-hemochromatotic iron overload: fact or fiction?. J Hepatol 49 (2008) 680-685
-
(2008)
J Hepatol
, vol.49
, pp. 680-685
-
-
Swinkels, D.W.1
Drenth, J.P.2
-
51
-
-
33646414765
-
A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia
-
Cappellini M.D., Cohen A., Piga A., Bejaoui M., Perrotta S., Agaoglu L., et al. A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with beta-thalassemia. Blood 107 (2006) 3455-3462
-
(2006)
Blood
, vol.107
, pp. 3455-3462
-
-
Cappellini, M.D.1
Cohen, A.2
Piga, A.3
Bejaoui, M.4
Perrotta, S.5
Agaoglu, L.6
-
52
-
-
36248933231
-
Guidelines on iron chelation therapy in patients with myelodysplastic syndromes and transfusional iron overload
-
Gattermann N. Guidelines on iron chelation therapy in patients with myelodysplastic syndromes and transfusional iron overload. Leuk Res 31 Suppl 3 (2007) S10-S15
-
(2007)
Leuk Res
, vol.31
, Issue.SUPPL. 3
-
-
Gattermann, N.1
|