-
1
-
-
0029843953
-
Thalassemia-a global public health problem
-
Weatherall DJ, Clegg JB. Thalassemia-a global public health problem. Nat Med 1996; 2: 847-849.
-
(1996)
Nat Med
, vol.2
, pp. 847-849
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
2
-
-
0033536288
-
The B-Thalassemias
-
Olivieri NF. The B-Thalassemias. N Engl J Med 1999; 341: 99-109.
-
(1999)
N Engl J Med
, vol.341
, pp. 99-109
-
-
Olivieri, N.F.1
-
3
-
-
0028212441
-
Present status of hemoglobinopathies in India
-
Marwah RK, Lal A. Present status of hemoglobinopathies in India. Indian Pediatr 1994;31:267-271.
-
(1994)
Indian Pediatr
, vol.31
, pp. 267-271
-
-
Marwah, R.K.1
Lal, A.2
-
5
-
-
0030022344
-
Clinical experience of management of thalassemia: The Sardinian experience
-
Cao A, Galanello R, Rosatelli MC, Argiolu F, Virgilils SD. Clinical experience of management of thalassemia: the Sardinian experience. Semin Hematol 1996;33:66-75.
-
(1996)
Semin Hematol
, vol.33
, pp. 66-75
-
-
Cao, A.1
Galanello, R.2
Rosatelli, M.C.3
Argiolu, F.4
Virgilils, S.D.5
-
6
-
-
0028086414
-
Survival in medically treated patients with homozygous beta thalassemia
-
Olivieri NF, Nathan DG, Macmillan JH, Wayne AS, Liu PP, McGee A, et al. Survival in medically treated patients with homozygous beta thalassemia. N Engl J Med 1994; 331: 574-578.
-
(1994)
N Engl J Med
, vol.331
, pp. 574-578
-
-
Olivieri, N.F.1
Nathan, D.G.2
Macmillan, J.H.3
Wayne, A.S.4
Liu, P.P.5
McGee, A.6
-
7
-
-
0031001278
-
Iron chelating therapy and treatment of thalassemia
-
Olivieri NF, Brittenham GM. Iron chelating therapy and treatment of thalassemia. Blood 1997; 89: 739-761.
-
(1997)
Blood
, vol.89
, pp. 739-761
-
-
Olivieri, N.F.1
Brittenham, G.M.2
-
8
-
-
0030995869
-
Beta thalassemia major and successful pregnancy
-
Kumar RM, Riak DE, Khurana A. Beta thalassemia major and successful pregnancy. J Reprod Med 1997; 42: 294-298.
-
(1997)
J Reprod Med
, vol.42
, pp. 294-298
-
-
Kumar, R.M.1
De Riak2
Khurana, A.3
-
9
-
-
0025138543
-
Removal of white cells from red cells by transfusion through a new filter
-
Sirchia G, Wenz B, Rebulla P. Removal of white cells from red cells by transfusion through a new filter. Transfusion 1990; 30: 30-33.
-
(1990)
Transfusion
, vol.30
, pp. 30-33
-
-
Sirchia, G.1
Wenz, B.2
Rebulla, P.3
-
10
-
-
0027463317
-
Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major
-
Brittenham GM, Cohen AR, McLaren CE, Martin MB, Griffith PM, Nienhuis AW et al. Hepatic iron stores and plasma ferritin concentration in patients with sickle cell anemia and thalassemia major. Am J Hematol 1993;42: 81-85.
-
(1993)
Am J Hematol
, vol.42
, pp. 81-85
-
-
Brittenham, G.M.1
Cohen, A.R.2
McLaren, C.E.3
Martin, M.B.4
Griffith, P.M.5
Nienhuis, A.W.6
-
11
-
-
0005395509
-
Hepatic iron concentrations and body iron stores determined by quantitative phlebotomy in patients cured of thalassemia major by bone marrow transplantation
-
a. abstract
-
Angelucci E, Giardini C, Brittenham GM Lucarelli G. Hepatic iron concentrations and body iron stores determined by quantitative phlebotomy in patients cured of thalassemia major by bone marrow transplantation. Blood 1997; 90: (Suppl 1): 265 a. abstract.
-
(1997)
Blood
, vol.90
, Issue.1 SUPPL.
, pp. 265
-
-
Angelucci, E.1
Giardini, C.2
Brittenham, G.M.3
Lucarelli, G.4
-
12
-
-
0031001278
-
Iron chelating therapy and the treatment of thalassemia
-
Erratum, Blood 1997, 89: 2621
-
Olivieri NF, Brittenham GM. Iron chelating therapy and the treatment of thalassemia. Blood 1997; 89: 739-761 [Erratum, Blood 1997, 89: 2621].
-
(1997)
Blood
, vol.89
, pp. 739-761
-
-
Olivieri, N.F.1
Brittenham, G.M.2
-
13
-
-
0020465049
-
Magnetic susceptibility measurements of human iron stores
-
Brittenham GM, Farrel DE, Harris JW. Magnetic susceptibility measurements of human iron stores. N Engl J Med 1982; 307: 1671-1675.
-
(1982)
N Engl J Med
, vol.307
, pp. 1671-1675
-
-
Brittenham, G.M.1
Farrel, D.E.2
Harris, J.W.3
-
14
-
-
0029363067
-
Iron overload in thalassemia: Comparative analysis of magnetic resonance imaging, serum ferritin and iron content of the liver
-
Mazza P, Gida R, De Moxo S, Bonetti MS, Amerri B, Magi C. Iron overload in thalassemia: Comparative analysis of magnetic resonance imaging, serum ferritin and iron content of the liver. Hematologica 1995; 80: 398-404.
-
(1995)
Hematologica
, vol.80
, pp. 398-404
-
-
Mazza, P.1
Gida, R.2
De Moxo, S.3
Bonetti, M.S.4
Amerri, B.5
Magi, C.6
-
15
-
-
0028059813
-
Efficacy of desferrioxamine in preventing complications of iron overload in patients with thalassemia major
-
Brittenham GM, Griffith PM, Nienhaus AW, Mclaren CE, Tucker EE, Alen CJ, et al. Efficacy of desferrioxamine in preventing complications of iron overload in patients with thalassemia major. N Engl J Med 1994; 331: 567-573.
-
(1994)
N Engl J Med
, vol.331
, pp. 567-573
-
-
Brittenham, G.M.1
Griffith, P.M.2
Nienhaus, A.W.3
Mclaren, C.E.4
Tucker, E.E.5
Alen, C.J.6
-
17
-
-
0025194869
-
Desferrioxamine: It's use in iron chelation in thalassemia
-
Sharma BK, Choudhury P, Dubey AP. Desferrioxamine: It's use in iron chelation in thalassemia. Indian Pediatr 1990; 27: 314-319.
-
(1990)
Indian Pediatr
, vol.27
, pp. 314-319
-
-
Sharma, B.K.1
Choudhury, P.2
Dubey, A.P.3
-
18
-
-
0030830275
-
Evaluation of a new method of administration of the iron chelating agent desferrioxamine
-
Borgna PC, Cohen A. Evaluation of a new method of administration of the iron chelating agent desferrioxamine. J Pediatr 1997; 130: 86-88.
-
(1997)
J Pediatr
, vol.130
, pp. 86-88
-
-
Borgna, P.C.1
Cohen, A.2
-
20
-
-
0023489829
-
Effective chelation of iron in thalassemia with the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-one
-
Kontoghiorges GJ, Aldouri MP, Hoffbrand AV, Barr J, Wonke B, Kourouclaris T, et al. Effective chelation of iron in thalassemia with the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-one. BMJ 1987; 295: 1509-1512.
-
(1987)
BMJ
, vol.295
, pp. 1509-1512
-
-
Kontoghiorges, G.J.1
Aldouri, M.P.2
Hoffbrand, A.V.3
Barr, J.4
Wonke, B.5
Kourouclaris, T.6
-
21
-
-
0026668939
-
Long term assessment of efficacy and safety of L1, an oral iron chelator in transfusion dependent thalassemia: Indian trial
-
Agarwal MB, Gupte SS, Vishwanathan C, Vasandani D, Ramanathan J, Desai N, et al. Long term assessment of efficacy and safety of L1, an oral iron chelator in transfusion dependent thalassemia: Indian trial. Br J Hematol 1992; 82: 460-466.
-
(1992)
Br J Hematol
, vol.82
, pp. 460-466
-
-
Agarwal, M.B.1
Gupte, S.S.2
Vishwanathan, C.3
Vasandani, D.4
Ramanathan, J.5
Desai, N.6
-
22
-
-
0029079707
-
Results of long term deferiprone (L1) therapy: A report by the International Study Group on oral iron chelators
-
Al-Refaie FN, Hershko C, Hoffbrand AV, Kosaryan, Olivieri, NF, Tondury. P, et al. Results of long term deferiprone (L1) therapy: A report by the International Study Group on oral iron chelators. Br J Hematol 1995: 91: 224-229.
-
(1995)
Br J Hematol
, vol.91
, pp. 224-229
-
-
Al-Refaie, F.N.1
Hershko, C.2
Hoffbrand, A.V.3
Kosaryan4
Olivieri, N.F.5
Tondury, P.6
-
23
-
-
0343836285
-
Thalassemia today
-
Olivieri NF. Thalassemia today. Acta Hematologica 1998; 100 (Suppl 1): 9.
-
(1998)
Acta Hematologica
, vol.100
, Issue.1 SUPPL.
, pp. 9
-
-
Olivieri, N.F.1
-
24
-
-
0342965344
-
Advances in iron chelating therapy
-
Piga A, Longo I, Voi V, Facello S, Tartaglia N. Advances in iron chelating therapy. Acta Hematologica 1998; 100 (Suppl 1): 270.
-
(1998)
Acta Hematologica
, vol.100
, Issue.1 SUPPL.
, pp. 270
-
-
Piga, A.1
Longo, I.2
Voi, V.3
Facello, S.4
Tartaglia, N.5
-
25
-
-
0030188555
-
Postsplenectomy care: Strategies to decrease the risk of infection
-
Williams DN, Kaur B. Postsplenectomy care: Strategies to decrease the risk of infection. Postgrad Med J 1996; 100: 195-205.
-
(1996)
Postgrad Med J
, vol.100
, pp. 195-205
-
-
Williams, D.N.1
Kaur, B.2
-
26
-
-
0032411128
-
High prevalence of low bone mass in thalassemia major
-
Jensen CE, Tuck SM, Agnew JE, Koneru S, Morris RW, Yardumian A, et al. High prevalence of low bone mass in thalassemia major. Br J Hematol 1998; 103: 911-915.
-
(1998)
Br J Hematol
, vol.103
, pp. 911-915
-
-
Jensen, C.E.1
Tuck, S.M.2
Agnew, J.E.3
Koneru, S.4
Morris, R.W.5
Yardumian, A.6
-
27
-
-
0030942974
-
Longitudinal monitoring of bone mineral density in thalassemia patients: Genetic structure and osteoporosis
-
Filosa A, Di Maio S, Vocca S, Saviano A, Esopotito G, Pagono L. Longitudinal monitoring of bone mineral density in thalassemia patients: Genetic structure and osteoporosis. Acata Pediatr 1997; 86: 342-346.
-
(1997)
Acata Pediatr
, vol.86
, pp. 342-346
-
-
Filosa, A.1
Di Maio, S.2
Vocca, S.3
Saviano, A.4
Esopotito, G.5
Pagono, L.6
-
28
-
-
0030867354
-
Short stature and failure of pubertal development in thalassemia major: Evidence hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotrophin secretion
-
Roth C, Pekrun A, Bartz M, Jarry H, Eber S, Lakomek M, et al. Short stature and failure of pubertal development in thalassemia major: Evidence hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotrophin secretion. Eur J Pediatr 1997; 156: 777-783.
-
(1997)
Eur J Pediatr
, vol.156
, pp. 777-783
-
-
Roth, C.1
Pekrun, A.2
Bartz, M.3
Jarry, H.4
Eber, S.5
Lakomek, M.6
-
29
-
-
0030016856
-
Can adrenarche influence the degree of osteopenia in thalassemic children?
-
Filosa A, Di Maio S, Saviano A, Vocca S, Esposito G. Can adrenarche influence the degree of osteopenia in thalassemic children? J Pediatr Endocrinol Metab 1996; 9: 401-406.
-
(1996)
J Pediatr Endocrinol Metab
, vol.9
, pp. 401-406
-
-
Filosa, A.1
Di Maio, S.2
Saviano, A.3
Vocca, S.4
Esposito, G.5
-
30
-
-
0029963993
-
Growth and development in thalassemia major patients with severe bone lesions due to desferrioxamine
-
De Sanctis V, Pinamonti A, Di Palma A, Sprocati M, Ahi G, Gamberini MR, et al. Growth and development in thalassemia major patients with severe bone lesions due to desferrioxamine. Eur J Pediatr 1996; 155: 368-372.
-
(1996)
Eur J Pediatr
, vol.155
, pp. 368-372
-
-
De Sanctis, V.1
Pinamonti, A.2
Di Palma, A.3
Sprocati, M.4
Ahi, G.5
Gamberini, M.R.6
-
31
-
-
0032411167
-
Osteopenia in female beta-thalassemic patients
-
Pafuni C, Roccasalva L, Pernicone G, Spano G, Palumbo MA, Gregorio FD, et al. Osteopenia in female beta-thalassemic patients. J Pediatr Endocrinol metab 1998; 11: 989-991.
-
(1998)
J Pediatr Endocrinol Metab
, vol.11
, pp. 989-991
-
-
Pafuni, C.1
Roccasalva, L.2
Pernicone, G.3
Spano, G.4
Palumbo, M.A.5
Gregorio, F.D.6
-
32
-
-
0032427820
-
Genetic and acquired predisposing factors and treatment of osteoporosis in thalassemia major
-
Wonke B, Jensen C, Hanslip JJ, Prescott E, Lalloz M, Layton M, et al. Genetic and acquired predisposing factors and treatment of osteoporosis in thalassemia major. J Pediatr Endocrinol Metab 1998; 11: 795-801.
-
(1998)
J Pediatr Endocrinol Metab
, vol.11
, pp. 795-801
-
-
Wonke, B.1
Jensen, C.2
Hanslip, J.J.3
Prescott, E.4
Lalloz, M.5
Layton, M.6
-
33
-
-
0033547031
-
Bone disease in beta thalassemia
-
Singer ST, Vichinsky EP. Bone disease in beta thalassemia (Commentary). Lancet 1999; 354: 881-882.
-
(1999)
Lancet
, vol.354
, pp. 881-882
-
-
Singer, S.T.1
Vichinsky, E.P.2
-
34
-
-
0018760153
-
Iron absorption in the thalassemia syndromes and its inhibition by tea
-
DeAlarcan PA, Donovan ME, Foebes GB, Landau SA, Stockam JA. Iron absorption in the thalassemia syndromes and its inhibition by tea. N Engl J Med 1979; 300: 5-8.
-
(1979)
N Engl J Med
, vol.300
, pp. 5-8
-
-
DeAlarcan, P.A.1
Donovan, M.E.2
Foebes, G.B.3
Landau, S.A.4
Stockam, J.A.5
-
35
-
-
0016652254
-
The effect of lea on iron absorption
-
Disler PB, Lynch SR, Charton RW, Torrance JD, Bothwell TH, Walker RB, et al. The effect of lea on iron absorption. Gut 1975; 16: 193-200.
-
(1975)
Gut
, vol.16
, pp. 193-200
-
-
Disler, P.B.1
Lynch, S.R.2
Charton, R.W.3
Torrance, J.D.4
Bothwell, T.H.5
Walker, R.B.6
-
38
-
-
13344276567
-
Marrow transplantation for patients with thalassemia: Results in class 3 patients
-
Lucarelli G, Clift RA, Galinberti M, Polchi P, Angelucci E, Baronciani D, et al. Marrow transplantation for patients with thalassemia: Results in class 3 patients. Blood 1996; 87: 2062-2088.
-
(1996)
Blood
, vol.87
, pp. 2062-2088
-
-
Lucarelli, G.1
Clift, R.A.2
Galinberti, M.3
Polchi, P.4
Angelucci, E.5
Baronciani, D.6
-
41
-
-
0025070260
-
Bone marrow transplantation in patients with thalassemia
-
Lucarelli G, Galimberti M, Polchi P, Angelucci E, Baronciani D, Giardini C, et al. Bone marrow transplantation in patients with thalassemia. N Engl J Med 1990; 322: 417-421.
-
(1990)
N Engl J Med
, vol.322
, pp. 417-421
-
-
Lucarelli, G.1
Galimberti, M.2
Polchi, P.3
Angelucci, E.4
Baronciani, D.5
Giardini, C.6
-
42
-
-
0343400554
-
Bone marrow transplantation in thalassemia
-
Giardnini C, Lucarelli G, Galinberti M, Baronciani D, Angelico E, Polchi P, et al. Bone marrow transplantation in thalassemia. Acta Hematologica 1998; 100 (Suppl 1): 284.
-
(1998)
Acta Hematologica
, vol.100
, Issue.1 SUPPL.
, pp. 284
-
-
Giardnini, C.1
Lucarelli, G.2
Galinberti, M.3
Baronciani, D.4
Angelico, E.5
Polchi, P.6
-
44
-
-
0028144365
-
Peripheral blood progenitor cells mobilized by G-CSF (Filgrastim) and rein fused as unprocessed autologous whole blood shorten the pancytopenic period following high dose melphalan in multiple myeloma
-
Ossenkoppele GJ, Jonkoff AR, Huihgens PC, Nauta JJP, Vander HKG, Drager AM. Peripheral blood progenitor cells mobilized by G-CSF (Filgrastim) and rein fused as unprocessed autologous whole blood shorten the pancytopenic period following high dose melphalan in multiple myeloma. Bone marrow Transplant 1994; 13: 37-41.
-
(1994)
Bone Marrow Transplant
, vol.13
, pp. 37-41
-
-
Ossenkoppele, G.J.1
Jonkoff, A.R.2
Huihgens, P.C.3
Nauta, J.J.P.4
Vander, H.K.G.5
Drager, A.M.6
-
45
-
-
0031155483
-
Hematopoictic Stem cell transplantation
-
Choudhry VP. Hematopoictic Stem cell transplantation. Indian Pediatr 1997; 34: 505-517.
-
(1997)
Indian Pediatr
, vol.34
, pp. 505-517
-
-
Choudhry, V.P.1
-
46
-
-
0029888485
-
Placental blood banking. A new frontier in transfusion medicine
-
Silberstein LE, Jefferies LC. Placental blood banking. A new frontier in transfusion medicine. N Engl J Med 1996; 335: 199-201.
-
(1996)
N Engl J Med
, vol.335
, pp. 199-201
-
-
Silberstein, L.E.1
Jefferies, L.C.2
-
47
-
-
8944228913
-
Placental blood as a source of hematopoietic stem cell for transplantation into unrelated recipients
-
Kurteber J, Laughlin M, Graham ML, Smith C, Olsan JF, Halperin EC, et al. Placental blood as a source of hematopoietic stem cell for transplantation into unrelated recipients. N Engl J Med 1996; 335: 157-166.
-
(1996)
N Engl J Med
, vol.335
, pp. 157-166
-
-
Kurteber, J.1
Laughlin, M.2
Graham, M.L.3
Smith, C.4
Olsan, J.F.5
Halperin, E.C.6
-
48
-
-
0029983013
-
Lack of evidence of permanent engraftment aller in utero fetal stem cell transplantation in congenital hemoglobinopathies
-
Westgren M, Ringden O, Eik-Nes S, Ek S, Anvret M, Brubakk AM, et al. Lack of evidence of permanent engraftment aller in utero fetal stem cell transplantation in congenital hemoglobinopathies. Transplantation 1996; 61: 1176-1179.
-
(1996)
Transplantation
, vol.61
, pp. 1176-1179
-
-
Westgren, M.1
Ringden, O.2
Eik-Nes, S.3
Ek, S.4
Anvret, M.5
Brubakk, A.M.6
-
49
-
-
0028303758
-
Mutagenesis of retroviral vectors transducing beta globin gene and beta globin locus control regioti derivates results in stable transmission of an active transcriptional structures
-
Leboutch P, Huang GS, Humphires RK. Mutagenesis of retroviral vectors transducing beta globin gene and beta globin locus control regioti derivates results in stable transmission of an active transcriptional structures. EMBO J 1994; 13: 3065-3076.
-
(1994)
EMBO J
, vol.13
, pp. 3065-3076
-
-
Leboutch, P.1
Huang, G.S.2
Humphires, R.K.3
-
50
-
-
0030065802
-
Towards gene therapy of hemoglobinopathies
-
Beuzard Y. Towards gene therapy of hemoglobinopathies. Semin Hematol 1996; 33: 43-52.
-
(1996)
Semin Hematol
, vol.33
, pp. 43-52
-
-
Beuzard, Y.1
-
51
-
-
0030910465
-
Formation of de novo centromeres and construction of first generation human artificial microsomes
-
Harrington SJ, Van Bokklen G, Mays RW. Formation of de novo centromeres and construction of first generation human artificial microsomes. Nature Genetics 1997; 4: 345-355.
-
(1997)
Nature Genetics
, vol.4
, pp. 345-355
-
-
Harrington, S.J.1
Van Bokklen, G.2
Mays, R.W.3
-
52
-
-
0028318417
-
A new bacteriophage P1 desired vector for the propagation of large human DNA fragments
-
Loqnnou PD, Amemiya CT, Garnes J, Kroisel PM, Shizuya H, Chen C, et al. A new bacteriophage P1 desired vector for the propagation of large human DNA fragments. Nature Genetics 1994; 6: 84-89.
-
(1994)
Nature Genetics
, vol.6
, pp. 84-89
-
-
Loqnnou, P.D.1
Amemiya, C.T.2
Garnes, J.3
Kroisel, P.M.4
Shizuya, H.5
Chen, C.6
-
53
-
-
0031949085
-
Genetic treatment of severe hemoglobinopathies: The combat against transgene variegation and transgenic silencing
-
Rivella S, Sadelain M. Genetic treatment of severe hemoglobinopathies: The combat against transgene variegation and transgenic silencing. Semin Hematol 1998; 35: 112-125.
-
(1998)
Semin Hematol
, vol.35
, pp. 112-125
-
-
Rivella, S.1
Sadelain, M.2
-
54
-
-
0027078611
-
A short term trial of butyrate to stimulate fetal globin gene expression in the beta-globin disorders
-
Perrine SP, Ginder GD, Faller DV, Dover GH, Ikuta J, Witkowska HE, et al. A short term trial of butyrate to stimulate fetal globin gene expression in the beta-globin disorders. N Engl J Med 1993; 328: 129-131.
-
(1993)
N Engl J Med
, vol.328
, pp. 129-131
-
-
Perrine, S.P.1
Ginder, G.D.2
Faller, D.V.3
Dover, G.H.4
Ikuta, J.5
Witkowska, H.E.6
-
55
-
-
0029257858
-
Butyrates in the treatment of sickle cell disease and beta thalassemia
-
Faller DV, Perrie SP. Butyrates in the treatment of sickle cell disease and beta thalassemia, Curr Opin Hematol 1995; 2: 109-117.
-
(1995)
Curr Opin Hematol
, vol.2
, pp. 109-117
-
-
Faller, D.V.1
Perrie, S.P.2
-
56
-
-
0030872518
-
Hematological responses to hydroxyurea therapy in multi transfused thalassemic children
-
Choudhry VP, Lal A, Pati HP, Arya LS. Hematological responses to hydroxyurea therapy in multi transfused thalassemic children. Indian J Pediatr 1997; 64: 395-398.
-
(1997)
Indian J Pediatr
, vol.64
, pp. 395-398
-
-
Choudhry, V.P.1
Lal, A.2
Pati, H.P.3
Arya, L.S.4
-
58
-
-
0030748791
-
Treatment of thalassemia major with phenylbutyrate and hydroxyurea
-
Olivieri NF, Rees DC, Ginder GD, Thein, Brittenham GM, Waye JS, et al. Treatment of thalassemia major with phenylbutyrate and hydroxyurea. Lancet 1997; 350: 491-492.
-
(1997)
Lancet
, vol.350
, pp. 491-492
-
-
Olivieri, N.F.1
Rees, D.C.2
Ginder, G.D.3
Thein4
Brittenham, G.M.5
Waye, J.S.6
-
59
-
-
0028837699
-
Novel treatment options in the severe B-globin disorders
-
Rodgers GP, Rachmilewitz EA. Novel treatment options in the severe B-globin disorders. Brit J Hematol 1995; 91: 263-268.
-
(1995)
Brit J Hematol
, vol.91
, pp. 263-268
-
-
Rodgers, G.P.1
Rachmilewitz, E.A.2
-
60
-
-
0028870221
-
Oral sodium phe-nylbutyrate therapy in homozygous beta thala-ssemia: A clinical trial
-
Collins AF, Pearson HA, Giardina P, McDonagh KT, Brusilow SW, Dover GJ. Oral sodium phe-nylbutyrate therapy in homozygous beta thala-ssemia: A clinical trial. Blood 1995; 85: 43-49.
-
(1995)
Blood
, vol.85
, pp. 43-49
-
-
Collins, A.F.1
Pearson, H.A.2
Giardina, P.3
McDonagh, K.T.4
Brusilow, S.W.5
Dover, G.J.6
-
61
-
-
0031728305
-
Heme arginate therapy for beta thalassemia: In vitro versus in vivo effects
-
Rind D, Fibach E, Goldfar BA, Friedbarg A, Rachmilewitz EA. Heme arginate therapy for beta thalassemia: in vitro versus in vivo effects. Acta Hematol 1998; 100: 82-84.
-
(1998)
Acta Hematol
, vol.100
, pp. 82-84
-
-
Rind, D.1
Fibach, E.2
Goldfar, B.A.3
Friedbarg, A.4
Rachmilewitz, E.A.5
-
62
-
-
0001692209
-
Administration of erythropoietin to patients with beta thalassemia intermedia: A preliminary trial
-
Rachmilewitz EA, Goldfarls A, Dover G, Administration of erythropoietin to patients with beta thalassemia intermedia: A preliminary trial. Blood 1991; 78: 1145-1147.
-
(1991)
Blood
, vol.78
, pp. 1145-1147
-
-
Rachmilewitz, E.A.1
Goldfarls, A.2
Dover, G.3
-
63
-
-
0027096261
-
Trial of recombinant human erythropoietin in thalassemia intermedia
-
Olivieri NF, Freedman M, Perrine S, Dover GJ, Sheridan B, Essentine DL, et al. Trial of recombinant human erythropoietin in thalassemia intermedia. Blood 1992; 80: 3258-3260.
-
(1992)
Blood
, vol.80
, pp. 3258-3260
-
-
Olivieri, N.F.1
Freedman, M.2
Perrine, S.3
Dover, G.J.4
Sheridan, B.5
Essentine, D.L.6
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