-
1
-
-
0000983253
-
Ferritin and ferruginous micelles in normal erythroblasts and hypochromic hypersideremic anemias
-
Bessis MC, Breton-Gorius J Ferritin and ferruginous micelles in normal erythroblasts and hypochromic hypersideremic anemias. Blood 1959, 14:423-432.
-
(1959)
Blood
, vol.14
, pp. 423-432
-
-
Bessis, M.C.1
Breton-Gorius, J.2
-
2
-
-
0014988440
-
Microspectrophotometric and electron microscopic studies of bone marrow in hereditary sideroblastic anaemia
-
Wickramasinghe SN, Fulker MJ, Losowsky MS, Hall R Microspectrophotometric and electron microscopic studies of bone marrow in hereditary sideroblastic anaemia. Acta Haematol 1971, 45:236-244.
-
(1971)
Acta Haematol
, vol.45
, pp. 236-244
-
-
Wickramasinghe, S.N.1
Fulker, M.J.2
Losowsky, M.S.3
Hall, R.4
-
3
-
-
0037372442
-
Mitochondrial ferritin expression in erythroid cells from patients with SA
-
Cazzola M, Invernizzi R, Bergamaschi G Mitochondrial ferritin expression in erythroid cells from patients with SA. Blood 2003, 101:1996-2000.
-
(2003)
Blood
, vol.101
, pp. 1996-2000
-
-
Cazzola, M.1
Invernizzi, R.2
Bergamaschi, G.3
-
4
-
-
67649699028
-
Sideroblastic anemias
-
Lippincott Williams & Wilkins, Philadelphia, J.P. Greer, J. Foerster, G.M. Rodgers
-
Bottomley SS Sideroblastic anemias. Wintrobe's Clinical Hematology 2008, 835-855. Lippincott Williams & Wilkins, Philadelphia. 12th ed. J.P. Greer, J. Foerster, G.M. Rodgers .
-
(2008)
Wintrobe's Clinical Hematology
, pp. 835-855
-
-
Bottomley, S.S.1
-
5
-
-
74849109450
-
Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations
-
Bergmann AK, Campagna DR, McLoughlin EM, et al. Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations. Pediatr Blood Cancer 2010, 54:273-278.
-
(2010)
Pediatr Blood Cancer
, vol.54
, pp. 273-278
-
-
Bergmann, A.K.1
Campagna, D.R.2
McLoughlin, E.M.3
-
6
-
-
0029027246
-
5-Aminolevulinate synthase and the first step of heme biosynthesis
-
Ferreira GC, Gong J 5-Aminolevulinate synthase and the first step of heme biosynthesis. J Bioenerg Biomembr 1995, 27:151-159.
-
(1995)
J Bioenerg Biomembr
, vol.27
, pp. 151-159
-
-
Ferreira, G.C.1
Gong, J.2
-
7
-
-
84964128174
-
Pyridoxine responsive anemia in the human adult
-
Harris JW, Whittington RM, Weisman R, Horrigan DL Pyridoxine responsive anemia in the human adult. Proc Soc Exp Biol Med 1956, 91:427-432.
-
(1956)
Proc Soc Exp Biol Med
, vol.91
, pp. 427-432
-
-
Harris, J.W.1
Whittington, R.M.2
Weisman, R.3
Horrigan, D.L.4
-
8
-
-
0031906394
-
The molecular biology and pyridoxine responsiveness of X-linked sideroblastic anaemia
-
May A, Bishop DF The molecular biology and pyridoxine responsiveness of X-linked sideroblastic anaemia. Haematologica 1998, 83:56-70.
-
(1998)
Haematologica
, vol.83
, pp. 56-70
-
-
May, A.1
Bishop, D.F.2
-
9
-
-
0034672159
-
Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females
-
Cazzola M, May A, Bergamaschi G, et al. Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females. Blood 2000, 96:4363-4365.
-
(2000)
Blood
, vol.96
, pp. 4363-4365
-
-
Cazzola, M.1
May, A.2
Bergamaschi, G.3
-
10
-
-
33745945731
-
X-linked sideroblastic anemia associated with a novel ALAS2 mutation and unfortunate skewed X-chromosome inactivation patterns
-
Aivado M, Gatterman N, Rong A, et al. X-linked sideroblastic anemia associated with a novel ALAS2 mutation and unfortunate skewed X-chromosome inactivation patterns. Blood Cells Mol Dis 2006, 37:40-45.
-
(2006)
Blood Cells Mol Dis
, vol.37
, pp. 40-45
-
-
Aivado, M.1
Gatterman, N.2
Rong, A.3
-
11
-
-
0000718795
-
Disorders of heme biosynthesis: X-linked sideroblastic anemia and the porphyrias
-
McGraw-Hill, New York, NY
-
Anderson KE, Sassa S, Bishop DF, Desnick RJ Disorders of heme biosynthesis: X-linked sideroblastic anemia and the porphyrias. The Metabolic and Molecular Bases of Inherited Disease 2001, Vol 2:2991-3062. McGraw-Hill, New York, NY. 8th ed.
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease
, vol.2
, pp. 2991-3062
-
-
Anderson, K.E.1
Sassa, S.2
Bishop, D.F.3
Desnick, R.J.4
-
12
-
-
0020664096
-
Iron overload in mild sideroblastic anaemias
-
Peto TE, Pippard MJ, Weatherall DJ Iron overload in mild sideroblastic anaemias. Lancet 1983, 1:375-378.
-
(1983)
Lancet
, vol.1
, Issue.8321
, pp. 375-378
-
-
Peto, T.E.1
Pippard, M.J.2
Weatherall, D.J.3
-
13
-
-
0033105568
-
Four new mutations in the erythroid-specific 5-aminolevulinate synthase gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis
-
Cotter PD, May A, Li L, et al. Four new mutations in the erythroid-specific 5-aminolevulinate synthase gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis. Blood 1999, 93:1757-1769.
-
(1999)
Blood
, vol.93
, pp. 1757-1769
-
-
Cotter, P.D.1
May, A.2
Li, L.3
-
14
-
-
0036893199
-
Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation
-
Cazzola M, May A, Bergamaschi G, et al. Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation. Blood 2002, 100:4236-4238.
-
(2002)
Blood
, vol.100
, pp. 4236-4238
-
-
Cazzola, M.1
May, A.2
Bergamaschi, G.3
-
15
-
-
0028875262
-
Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta;-aminolevulinate synthase gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts
-
Cotter PD, May A, Fitzsimons EJ, et al. Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid δ-aminolevulinate synthase gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts. J Clin Invest 1995, 96:2090-2096.
-
(1995)
J Clin Invest
, vol.96
, pp. 2090-2096
-
-
Cotter, P.D.1
May, A.2
Fitzsimons, E.J.3
-
16
-
-
0038650906
-
5-Aminolevulinic acid synthase: mechanism, mutations and medicine
-
Shoolingin-Jordan PM, Al-Daihan S, Alexeev D, et al. 5-Aminolevulinic acid synthase: mechanism, mutations and medicine. Biochim Biophys Acta 2003, 1647:361-366.
-
(2003)
Biochim Biophys Acta
, vol.1647
, pp. 361-366
-
-
Shoolingin-Jordan, P.M.1
Al-Daihan, S.2
Alexeev, D.3
-
17
-
-
25144499698
-
Crystal structure of 5-aminolevulinate synthase, the first enzyme of heme biosynthesis, and its link to XLSA in humans
-
Astner I, Schulze JO, Van Den Hevel J, et al. Crystal structure of 5-aminolevulinate synthase, the first enzyme of heme biosynthesis, and its link to XLSA in humans. EMBO J 2005, 24:3166-3177.
-
(2005)
EMBO J
, vol.24
, pp. 3166-3177
-
-
Astner, I.1
Schulze, J.O.2
Van Den Hevel, J.3
-
18
-
-
0030752517
-
Pyridoxine refractory X-linked sideroblastic anemia caused by a point mutation in the erythroid 5-aminolevulinate synthase gene
-
Furuyama K, Fujita H, Nagai T, et al. Pyridoxine refractory X-linked sideroblastic anemia caused by a point mutation in the erythroid 5-aminolevulinate synthase gene. Blood 1997, 90:822-830.
-
(1997)
Blood
, vol.90
, pp. 822-830
-
-
Furuyama, K.1
Fujita, H.2
Nagai, T.3
-
19
-
-
51149108520
-
C-terminal deletions in the ALAS2 gene lead to gain of function and cause a previously undefined type of human porphyria, X-linked dominant protoporphyria, without anemia or iron overload
-
Whatley SD, Ducamp S, Gouya L, et al. C-terminal deletions in the ALAS2 gene lead to gain of function and cause a previously undefined type of human porphyria, X-linked dominant protoporphyria, without anemia or iron overload. Am J Hum Genet 2008, 83:408-414.
-
(2008)
Am J Hum Genet
, vol.83
, pp. 408-414
-
-
Whatley, S.D.1
Ducamp, S.2
Gouya, L.3
-
20
-
-
6344220330
-
Onset of X-linked sideroblastic anemia in the fourth decade
-
Cortesao E, Vidan J, Pereira J, et al. Onset of X-linked sideroblastic anemia in the fourth decade. Haematologica 2004, 89:1261-1263.
-
(2004)
Haematologica
, vol.89
, pp. 1261-1263
-
-
Cortesao, E.1
Vidan, J.2
Pereira, J.3
-
21
-
-
0021926630
-
Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder
-
Pagon RA, Bird TD, Detter JC, Pierce I Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder. J Med Genet 1985, 22:267-273.
-
(1985)
J Med Genet
, vol.22
, pp. 267-273
-
-
Pagon, R.A.1
Bird, T.D.2
Detter, J.C.3
Pierce, I.4
-
22
-
-
0032920837
-
Mutation of a putative mitochondrial iron transporter gene in X-linked sideroblastic anemia and ataxia
-
Allikmets R, Raskind WH, Hutchinson A, et al. Mutation of a putative mitochondrial iron transporter gene (ABCB7) in X-linked sideroblastic anemia and ataxia . Hum Mol Genet 1999, 8:743-749.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 743-749
-
-
Allikmets, R.1
Raskind, W.H.2
Hutchinson, A.3
-
23
-
-
0034329310
-
Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation
-
Bekri S, Kispal G, Lange H, et al. Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation. Blood 2000, 96:3256-3264.
-
(2000)
Blood
, vol.96
, pp. 3256-3264
-
-
Bekri, S.1
Kispal, G.2
Lange, H.3
-
24
-
-
0035672913
-
X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L
-
Maguire A, Hellier K, Hammans S, May A X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L. Br J Haematol 2001, 115:910-917.
-
(2001)
Br J Haematol
, vol.115
, pp. 910-917
-
-
Maguire, A.1
Hellier, K.2
Hammans, S.3
May, A.4
-
25
-
-
34147165135
-
RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload
-
Cavadini P, Biasiotto G, Poli M, et al. RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload. Blood 2007, 109:3552-3559.
-
(2007)
Blood
, vol.109
, pp. 3552-3559
-
-
Cavadini, P.1
Biasiotto, G.2
Poli, M.3
-
27
-
-
68949128587
-
Function and biogenesis of iron-sulphur proteins
-
Lill R Function and biogenesis of iron-sulphur proteins. Nature 2009, 460:831-838.
-
(2009)
Nature
, vol.460
, pp. 831-838
-
-
Lill, R.1
-
28
-
-
0025822118
-
Identification of a novel iron-responsive element in murine and human erythroid delta;-aminolevulinic acid synthase mRNA
-
Dandekar T, Stripecke R, Gray NK, et al. Identification of a novel iron-responsive element in murine and human erythroid δ-aminolevulinic acid synthase mRNA. EMBO J 1991, 10:1903-1909.
-
(1991)
EMBO J
, vol.10
, pp. 1903-1909
-
-
Dandekar, T.1
Stripecke, R.2
Gray, N.K.3
-
29
-
-
67349267792
-
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
-
Guernsey DL, Jiang H, Campagna DR, et al. Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nat Genet 2009, 41:651-653.
-
(2009)
Nat Genet
, vol.41
, pp. 651-653
-
-
Guernsey, D.L.1
Jiang, H.2
Campagna, D.R.3
-
30
-
-
34548013116
-
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
-
Camaschella C, Campanella A, De Falco L, et al. The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. Blood 2007, 110:1353-1358.
-
(2007)
Blood
, vol.110
, pp. 1353-1358
-
-
Camaschella, C.1
Campanella, A.2
De Falco, L.3
-
31
-
-
23944500052
-
Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis
-
Wingert RA, Galloway JL, Barut B, et al. Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis. Nature 2005, 436:1035-1039.
-
(2005)
Nature
, vol.436
, pp. 1035-1039
-
-
Wingert, R.A.1
Galloway, J.L.2
Barut, B.3
-
32
-
-
0028817474
-
Myopathy, lactic acidosis, and sideroblastic anemia: a new syndrome
-
Inbal A, Avissar N, Shaklai M, et al. Myopathy, lactic acidosis, and sideroblastic anemia: a new syndrome. Am J Med Genet 1995, 55:372-378.
-
(1995)
Am J Med Genet
, vol.55
, pp. 372-378
-
-
Inbal, A.1
Avissar, N.2
Shaklai, M.3
-
33
-
-
1442308549
-
Mitochondrial myopathy and sideroblastic anaemia
-
Casas KA, Fischel-Ghodsian N Mitochondrial myopathy and sideroblastic anaemia. Am J Med Genet 2004, 125A:201-204.
-
(2004)
Am J Med Genet
, vol.125 A
, pp. 201-204
-
-
Casas, K.A.1
Fischel-Ghodsian, N.2
-
34
-
-
34147144142
-
Nonsense mutation in pseudouridylate synthase 1 in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia
-
Fernandez-Vizarra E, Berardinelli A, Valente L, et al. Nonsense mutation in pseudouridylate synthase 1 in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia . J Med Genet 2007, 44:173-180.
-
(2007)
J Med Genet
, vol.44
, pp. 173-180
-
-
Fernandez-Vizarra, E.1
Berardinelli, A.2
Valente, L.3
-
35
-
-
77955061839
-
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia-MLASA syndrome
-
Riley LG, Cooper S, Hickey P, et al. Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia-MLASA syndrome. Am J Hum Genet 2010, 87:52-59.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 52-59
-
-
Riley, L.G.1
Cooper, S.2
Hickey, P.3
-
37
-
-
73949095906
-
Thiamine-responsive megaloblastic anemia: identification of novel heterozygotes and mutation update
-
Bergmann AK, Sahai I, Falcone JF, et al. Thiamine-responsive megaloblastic anemia: identification of novel heterozygotes and mutation update. J Pediatr 2009, 155:888-892.
-
(2009)
J Pediatr
, vol.155
, pp. 888-892
-
-
Bergmann, A.K.1
Sahai, I.2
Falcone, J.F.3
-
38
-
-
0033064140
-
The gene mutated in thiamine-responsive anemia with diabetes and deafness encodes a functional thiamine transporter
-
Fleming JC, Tartaglini E, Steinkamp MP, et al. The gene mutated in thiamine-responsive anemia with diabetes and deafness encodes a functional thiamine transporter. Nat Genet 1999, 22:305-308.
-
(1999)
Nat Genet
, vol.22
, pp. 305-308
-
-
Fleming, J.C.1
Tartaglini, E.2
Steinkamp, M.P.3
-
39
-
-
0035053717
-
Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport
-
Neufeld EJ, Fleming JC, Tartaglini E, Steinkamp MP Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport. Blood Cells Mol Dis 2001, 27:135-138.
-
(2001)
Blood Cells Mol Dis
, vol.27
, pp. 135-138
-
-
Neufeld, E.J.1
Fleming, J.C.2
Tartaglini, E.3
Steinkamp, M.P.4
-
40
-
-
29944432489
-
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families
-
Ricketts CJ, Minton JA, Samuel J, et al. Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. Acta Paediatr 2006, 95:99-104.
-
(2006)
Acta Paediatr
, vol.95
, pp. 99-104
-
-
Ricketts, C.J.1
Minton, J.A.2
Samuel, J.3
-
41
-
-
0023262565
-
Hereditary sideroblastic anaemia and autosomal inheritance of erythrocyte dimorphism in a Dutch family
-
van Waveren Hogervorst GD, van Roermund HPC, Snijders PJ Hereditary sideroblastic anaemia and autosomal inheritance of erythrocyte dimorphism in a Dutch family. Eur J Haematol 1987, 38:405-409.
-
(1987)
Eur J Haematol
, vol.38
, pp. 405-409
-
-
van Waveren Hogervorst, G.D.1
van Roermund, H.P.C.2
Snijders, P.J.3
-
42
-
-
0030922559
-
A novel form of hereditary sideroblastic anaemia with macrocytosis
-
Tuckfield A, Ratnaike S, Hussein S, Metz J A novel form of hereditary sideroblastic anaemia with macrocytosis. Br J Haematol 1997, 97:279-285.
-
(1997)
Br J Haematol
, vol.97
, pp. 279-285
-
-
Tuckfield, A.1
Ratnaike, S.2
Hussein, S.3
Metz, J.4
-
43
-
-
0018712317
-
A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction
-
Pearson HA, Lobel JS, Kocoshis SA, et al. A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction. J Pediatr 1979, 95:976-984.
-
(1979)
J Pediatr
, vol.95
, pp. 976-984
-
-
Pearson, H.A.1
Lobel, J.S.2
Kocoshis, S.A.3
-
44
-
-
0025133424
-
Pearson's marrow-pancreas syndrome: a multisystem mitochondrial disorder in infancy
-
Rotig A, Cormier V, Blanche S, et al. Pearson's marrow-pancreas syndrome: a multisystem mitochondrial disorder in infancy. J Clin Invest 1990, 86:1601-1608.
-
(1990)
J Clin Invest
, vol.86
, pp. 1601-1608
-
-
Rotig, A.1
Cormier, V.2
Blanche, S.3
-
45
-
-
0025968682
-
Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA
-
McShane MA, Hammans SR, Sweeney M, et al. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. Am J Hum Genet 1991, 48:39-42.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 39-42
-
-
McShane, M.A.1
Hammans, S.R.2
Sweeney, M.3
-
47
-
-
77956906221
-
Anemia in a patient newly transferred from peritoneal dialysis to hemodialysis
-
Gill H, Yip T, Lo W-K Anemia in a patient newly transferred from peritoneal dialysis to hemodialysis. Am J Kid Dis 2010, 56:xxxvii-xxxvix.
-
(2010)
Am J Kid Dis
, vol.56
, pp. 37-39
-
-
Gill, H.1
Yip, T.2
Lo, W.-K.3
-
48
-
-
0036786901
-
The World Health Organization classification of the myeloid neoplasms
-
Vardiman JW, Harris NL, Brunning RD The World Health Organization classification of the myeloid neoplasms. Blood 2002, 100:2292-2302.
-
(2002)
Blood
, vol.100
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
49
-
-
13444269356
-
Myelodysplastic syndromes - coping with ineffective hematopoiesis
-
Cazzola M, Malcovati L Myelodysplastic syndromes - coping with ineffective hematopoiesis. New Engl J Med 2005, 352:536-538.
-
(2005)
New Engl J Med
, vol.352
, Issue.6
, pp. 536-538
-
-
Cazzola, M.1
Malcovati, L.2
-
50
-
-
34548219420
-
Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes
-
Malcovati L, Germing U, Kuendgen A, et al. Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes. J Clin Oncol 2007, 25:3503-3510.
-
(2007)
J Clin Oncol
, vol.25
, pp. 3503-3510
-
-
Malcovati, L.1
Germing, U.2
Kuendgen, A.3
-
51
-
-
0024423029
-
Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts
-
Dewald GW, Brecher M, Travis LB, Stupca PJ Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genet Cytogenet 1989, 42:173-185.
-
(1989)
Cancer Genet Cytogenet
, vol.42
, pp. 173-185
-
-
Dewald, G.W.1
Brecher, M.2
Travis, L.B.3
Stupca, P.J.4
-
52
-
-
0037272767
-
Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes
-
Bowen D, Culligan D, Jowitt S, et al. Guidelines for the diagnosis and therapy of adult myelodysplastic syndromes. Br J Haematol 2003, 120:187-200.
-
(2003)
Br J Haematol
, vol.120
, pp. 187-200
-
-
Bowen, D.1
Culligan, D.2
Jowitt, S.3
-
53
-
-
39649114580
-
Supportive care, growth factors, and new therapies in myelodysplastic syndromes
-
Hellström-Lindberg E, Malcovati L Supportive care, growth factors, and new therapies in myelodysplastic syndromes. Blood Rev 2008, 22:75-91.
-
(2008)
Blood Rev
, vol.22
, pp. 75-91
-
-
Hellström-Lindberg, E.1
Malcovati, L.2
-
54
-
-
44849143798
-
The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts
-
Boultwood J, Pellagatti A, Nikpour M, et al. The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts. PLoS One 2008, 3:e1970.
-
(2008)
PLoS One
, vol.3
-
-
Boultwood, J.1
Pellagatti, A.2
Nikpour, M.3
-
55
-
-
70449486011
-
Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
-
Malcovati L, Della Porta MG, Pietra D, et al. Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis. Blood 2009, 114:3538-3545.
-
(2009)
Blood
, vol.114
, pp. 3538-3545
-
-
Malcovati, L.1
Della Porta, M.G.2
Pietra, D.3
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