-
1
-
-
0004198466
-
The Thalassemia Syndromes
-
Weatherall DJ Clegg JB The Thalassemia Syndromes 1981 Blackwell Scientific Publications Oxford UK
-
(1981)
-
-
Weatherall, DJ1
Clegg, JB2
-
2
-
-
0014746252
-
The hemoglobin constitution of infants with the haemoglobin Bart's hydrops fetalis syndrome
-
Weatherall DJ Clegg JB Boon WH The hemoglobin constitution of infants with the haemoglobin Bart's hydrops fetalis syndrome Br J Haematol 18 1970 357 367
-
(1970)
Br J Haematol
, vol.18
, pp. 357-367
-
-
Weatherall, DJ1
Clegg, JB2
Boon, WH3
-
3
-
-
0027204744
-
Increased HbF in adult life
-
Wood WG Increased HbF in adult life Clin Haematol 6 1993 177 213
-
(1993)
Clin Haematol
, vol.6
, pp. 177-213
-
-
Wood, WG1
-
4
-
-
0022457460
-
Survival of a hydropic infant with homozygous α-thalassemia-1
-
Beaudry MA Ferguson DJ Pearse K Survival of a hydropic infant with homozygous α-thalassemia-1 J Pediatr 108 1986 713 716
-
(1986)
J Pediatr
, vol.108
, pp. 713-716
-
-
Beaudry, MA1
Ferguson, DJ2
Pearse, K3
-
5
-
-
0022544938
-
Normal long-term survival with α-thalassemia
-
Bianchi DW Beyer EC Stark AR Normal long-term survival with α-thalassemia J Pediatr 108 1986 716 718
-
(1986)
J Pediatr
, vol.108
, pp. 716-718
-
-
Bianchi, DW1
Beyer, EC2
Stark, AR3
-
6
-
-
0027052050
-
Long-term survival of a baby with homozygous alpha-thalassemia-1
-
Lam T-K Chan V Fok T-F Long-term survival of a baby with homozygous alpha-thalassemia-1 Acta Haematol 88 1992 198 200
-
(1992)
Acta Haematol
, vol.88
, pp. 198-200
-
-
Lam, T-K1
Chan, V2
Fok, T-F3
-
7
-
-
85114528593
-
Limb reduction defects in an infant with homozygous alpha thalassemia
-
(abstr) Abuelo DN Forman E Limb reduction defects in an infant with homozygous alpha thalassemia Presented at the Second Joint Clinical Genetics Meeting 1995
-
(1995)
-
-
Abuelo, DN1
Forman, E2
-
8
-
-
0028964326
-
Intrauterine therapy for homozygous a-thalassemia
-
Carr S Rubin L Dixon D Intrauterine therapy for homozygous a-thalassemia Obstet Gynecol 85 1995 876 879
-
(1995)
Obstet Gynecol
, vol.85
, pp. 876-879
-
-
Carr, S1
Rubin, L2
Dixon, D3
-
9
-
-
0028086414
-
Survival in medically treated patients with homozygous β thalassemia
-
Olivieri NF Nathan DG MacMillan JH Survival in medically treated patients with homozygous β thalassemia N Engl J Med 331 1994 574 578
-
(1994)
N Engl J Med
, vol.331
, pp. 574-578
-
-
Olivieri, NF1
Nathan, DG2
MacMillan, JH3
-
10
-
-
0028059813
-
Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major
-
Brittenham GM Griffith PM Nienhuis AW Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major N Engl J Med 331 1994 567 573
-
(1994)
N Engl J Med
, vol.331
, pp. 567-573
-
-
Brittenham, GM1
Griffith, PM2
Nienhuis, AW3
-
11
-
-
0027184519
-
Marrow transplantation in patients with thalassemia responsive to iron chelation therapy
-
Lucarelli G Galimberti M Polchi P Marrow transplantation in patients with thalassemia responsive to iron chelation therapy N Engl J Med 329 1993 840 844
-
(1993)
N Engl J Med
, vol.329
, pp. 840-844
-
-
Lucarelli, G1
Galimberti, M2
Polchi, P3
-
12
-
-
0021152512
-
Termination of pregnancy during the third trimester
-
Machin GA Popkin JS Styles S Termination of pregnancy during the third trimester N Engl J Med 311 1984 264 265
-
(1984)
N Engl J Med
, vol.311
, pp. 264-265
-
-
Machin, GA1
Popkin, JS2
Styles, S3
-
13
-
-
0025313516
-
Southeast Asian immigrants: The new thalassemias in America
-
Anderson HM Ranney HM Southeast Asian immigrants: The new thalassemias in America Semin Hematol 27 1990 239 246
-
(1990)
, pp. 239-246
-
-
Anderson, HM1
Ranney, HM2
-
14
-
-
0023859033
-
Levels of fetal hemoglobin necessary for the treatment of sickle cell disease
-
Noguchi CT Rodgers GP Serjeant G Levels of fetal hemoglobin necessary for the treatment of sickle cell disease N Engl J Med 318 1988 96 99
-
(1988)
N Engl J Med
, vol.318
, pp. 96-99
-
-
Noguchi, CT1
Rodgers, GP2
Serjeant, G3
-
15
-
-
0017641722
-
Participation of hemoglobins A and F in polymerization of sickle hemoglobin
-
Goldberg MA Husson MA Bunn HF Participation of hemoglobins A and F in polymerization of sickle hemoglobin J Biol Chem 252 1977 3414 3421
-
(1977)
J Biol Chem
, vol.252
, pp. 3414-3421
-
-
Goldberg, MA1
Husson, MA2
Bunn, HF3
-
17
-
-
0018969574
-
Hb F synthesis in sickle cell anemia: A comparison of Saudi Arab cases with those of African origin
-
Wood WG Pembrey ME Serjeant GR Hb F synthesis in sickle cell anemia: A comparison of Saudi Arab cases with those of African origin Br J Haematol 45 1980 431 445
-
(1980)
Br J Haematol
, vol.45
, pp. 431-445
-
-
Wood, WG1
Pembrey, ME2
Serjeant, GR3
-
18
-
-
0021931288
-
Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes
-
Brittenham GM Schechter AN Noguchi CT Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes Blood 65 1985 183 189
-
(1985)
Blood
, vol.65
, pp. 183-189
-
-
Brittenham, GM1
Schechter, AN2
Noguchi, CT3
-
19
-
-
30944436542
-
Genotype-phenotype correlations in -thalassemias
-
Cao A Galanello R Rosatelli MC Genotype-phenotype correlations in -thalassemias Blood Rev 8 1994 1 12
-
(1994)
Blood Rev
, vol.8
, pp. 1-12
-
-
Cao, A1
Galanello, R2
Rosatelli, MC3
-
20
-
-
85114537179
-
-
Serjeant GR Sickle Cell Disease 1992 Oxford University Press Oxford, UK 369 378
-
(1992)
, pp. 369-378
-
-
Serjeant, GR1
-
21
-
-
0018142844
-
Fetal hemoglobin production and the sickle gene in the Oases of eastern Saudi Arabia
-
Pembrey ME Wood WG Weatherall DJ Fetal hemoglobin production and the sickle gene in the Oases of eastern Saudi Arabia Br J Haematol 40 1978 415 429
-
(1978)
Br J Haematol
, vol.40
, pp. 415-429
-
-
Pembrey, ME1
Wood, WG2
Weatherall, DJ3
-
23
-
-
0020961106
-
Developmental genetics of the human hemoglobins
-
Wood WG Weatherall DJ Developmental genetics of the human hemoglobins Biochem J 215 1983 1 10
-
(1983)
Biochem J
, vol.215
, pp. 1-10
-
-
Wood, WG1
Weatherall, DJ2
-
24
-
-
0030039970
-
Reactivation of fetal hemoglobin in patients with thalassemia
-
Olivieri NF Reactivation of fetal hemoglobin in patients with thalassemia Semin Hematol 33 1996 24 42
-
(1996)
, pp. 24-42
-
-
Olivieri, NF1
-
25
-
-
0025653912
-
Fetal hemoglobin, sickling, and sickle cell disease
-
Charache S Fetal hemoglobin, sickling, and sickle cell disease Adv Pediatr 37 1990 1 31
-
(1990)
Adv Pediatr
, vol.37
, pp. 1-31
-
-
Charache, S1
-
26
-
-
0024446352
-
Mortality in children and adolescents with sickle cell disease
-
Leikin SL Gallagher D Kinney TR Mortality in children and adolescents with sickle cell disease Pediatrics 84 1989 500 508
-
(1989)
Pediatrics
, vol.84
, pp. 500-508
-
-
Leikin, SL1
Gallagher, D2
Kinney, TR3
-
27
-
-
0028291736
-
Mortality in sickle cell disease: Life expectancy and risk factors for early death
-
Platt OS Brambilla DJ Rosse WF Mortality in sickle cell disease: Life expectancy and risk factors for early death N Engl J Med 330 1994 1639 1644
-
(1994)
N Engl J Med
, vol.330
, pp. 1639-1644
-
-
Platt, OS1
Brambilla, DJ2
Rosse, WF3
-
28
-
-
0029025475
-
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia
-
Charache S Terrin ML Moore RD Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia N Engl J Med 332 1995 1317 1322
-
(1995)
N Engl J Med
, vol.332
, pp. 1317-1322
-
-
Charache, S1
Terrin, ML2
Moore, RD3
-
29
-
-
0345681889
-
Hydroxyurea increases HbF production in children with sickle cell disease
-
(abstr) Ohene-Frempong K Horiuchi K Bulgarelli W Hydroxyurea increases HbF production in children with sickle cell disease Blood 82 1993 472a
-
(1993)
Blood
, vol.82
, pp. 472a
-
-
Ohene-Frempong, K1
Horiuchi, K2
Bulgarelli, W3
-
30
-
-
0013003728
-
Clinical and hematological response of sickle cell children to treatment with hydroxyurea
-
(abstr) de Montalembert Belloy M Bernaudin F Clinical and hematological response of sickle cell children to treatment with hydroxyurea Blood 84 1994 219a
-
(1994)
Blood
, vol.84
, pp. 219a
-
-
de Montalembert1
Belloy, M2
Bernaudin, F3
-
31
-
-
85114541982
-
Hydroxyurea therapy in severely affected children with sickle cell disease
-
(abstr) Labotka RJ Misiewicz VM Robinson E Hydroxyurea therapy in severely affected children with sickle cell disease Pediatr Res 35 1994 163a
-
(1994)
Pediatr Res
, vol.35
, pp. 163a
-
-
Labotka, RJ1
Misiewicz, VM2
Robinson, E3
-
32
-
-
0029982591
-
Hydroxyurea therapy in children severely affected with sickle cell disease
-
Scott JP Hillery CA Brown ER Hydroxyurea therapy in children severely affected with sickle cell disease J Pediatr 128 1996 820 828
-
(1996)
J Pediatr
, vol.128
, pp. 820-828
-
-
Scott, JP1
Hillery, CA2
Brown, ER3
-
33
-
-
4243386935
-
Hydroxyurea in children with sickle cell disease
-
(abstr) Olivieri NF Basran R Nisbet-Brown E Hydroxyurea in children with sickle cell disease Blood 88 1996 621a
-
(1996)
Blood
, vol.88
, pp. 621a
-
-
Olivieri, NF1
Basran, R2
Nisbet-Brown, E3
-
35
-
-
0344015345
-
Hydroxyurea increases red cell pit counts in children and adolescents with sickle cell anemia: implications for assessment of splenic function
-
(abstr) Lane PA O'Connell JL Kinney TR Hydroxyurea increases red cell pit counts in children and adolescents with sickle cell anemia: implications for assessment of splenic function Blood 86 1995 140a
-
(1995)
Blood
, vol.86
, pp. 140a
-
-
Lane, PA1
O'Connell, JL2
Kinney, TR3
-
36
-
-
0005185293
-
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea
-
(abstr) Steinberg MH Lu Z-H Barton F Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea Blood 86 1995 418a
-
(1995)
Blood
, vol.86
, pp. 418a
-
-
Steinberg, MH1
Lu, Z-H2
Barton, F3
-
37
-
-
0008613003
-
Hydroxyurea improves erythropoiesis in a patient with homozygous beta thalassemia
-
(abstr) McDonagh KT Orringer EP Dover GJ Hydroxyurea improves erythropoiesis in a patient with homozygous beta thalassemia Clin Res 38 1990 346A
-
(1990)
Clin Res
, vol.38
, pp. 346A
-
-
McDonagh, KT1
Orringer, EP2
Dover, GJ3
-
38
-
-
0022273995
-
Pharmacological manipulation of fetal hemoglobin synthesis in patients with severe beta thalassemia
-
Nienhuis AW Ley TJ Humphries RK Pharmacological manipulation of fetal hemoglobin synthesis in patients with severe beta thalassemia Ann NY Acad Sci 445 1985 198 211
-
(1985)
Ann NY Acad Sci
, vol.445
, pp. 198-211
-
-
Nienhuis, AW1
Ley, TJ2
Humphries, RK3
-
39
-
-
0003014761
-
Clinical trials with hydroxyurea and recombinant human erythropoietin, in Stamatoyannopoulos G
-
Loukopoulos D Voskaridou E Stamoulakatou A Clinical trials with hydroxyurea and recombinant human erythropoietin, in Stamatoyannopoulos G Nienhuis AW Hemoglobin Switching 1995 Alan R. Liss New York, NY 365 372
-
(1995)
, pp. 365-372
-
-
Loukopoulos, D1
Voskaridou, E2
Stamoulakatou, A3
-
40
-
-
13344259315
-
Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/hemoglobin E disease
-
Fucharoen S Siritanaratkul N Winichagoon P Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/hemoglobin E disease Blood 87 1996 887 892
-
(1996)
Blood
, vol.87
, pp. 887-892
-
-
Fucharoen, S1
Siritanaratkul, N2
Winichagoon, P3
-
41
-
-
0027078611
-
A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders
-
Perrine SP Ginder GD Faller DV A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders N Engl J Med 328 1993 81 86
-
(1993)
N Engl J Med
, vol.328
, pp. 81-86
-
-
Perrine, SP1
Ginder, GD2
Faller, DV3
-
42
-
-
85114537571
-
Extended therapy with arginine butyrate in patients with thalassemia and sickle cell disease
-
Sher GD Ginder G Little JA Extended therapy with arginine butyrate in patients with thalassemia and sickle cell disease N Engl J Med 332 1995 106 110
-
(1995)
N Engl J Med
, vol.332
, pp. 106-110
-
-
Sher, GD1
Ginder, G2
Little, JA3
-
43
-
-
0028870221
-
Oral sodium phenylbutyrate therapy in homozygous beta thalassemia
-
Collins AF Pearson HA Giardina P Oral sodium phenylbutyrate therapy in homozygous beta thalassemia Blood 85 1995 43 49
-
(1995)
Blood
, vol.85
, pp. 43-49
-
-
Collins, AF1
Pearson, HA2
Giardina, P3
-
44
-
-
0001692209
-
Administration of erythropoietin to patients with β-thalassemia intermedia: A preliminary trial
-
Rachmilewitz EA Goldfarb A Dover G Administration of erythropoietin to patients with β-thalassemia intermedia: A preliminary trial Blood 78 1991 1145 1147
-
(1991)
Blood
, vol.78
, pp. 1145-1147
-
-
Rachmilewitz, EA1
Goldfarb, A2
Dover, G3
-
45
-
-
0027096261
-
Trial of recombinant human erythropoietin in thalassemia intermedia
-
Olivieri NF Freedman M Perrine S Trial of recombinant human erythropoietin in thalassemia intermedia Blood 80 1992 3258 3260
-
(1992)
Blood
, vol.80
, pp. 3258-3260
-
-
Olivieri, NF1
Freedman, M2
Perrine, S3
-
46
-
-
0029044458
-
Sustained increase in haemoglobin and RBC following long-term administration of recombinant human erythropoietin to patients with homozygous beta thalassemia
-
Rachmilewitz EA Aker M Perry D Sustained increase in haemoglobin and RBC following long-term administration of recombinant human erythropoietin to patients with homozygous beta thalassemia Br J Haematol 90 1995 341 345
-
(1995)
Br J Haematol
, vol.90
, pp. 341-345
-
-
Rachmilewitz, EA1
Aker, M2
Perry, D3
-
47
-
-
0027274649
-
Brief report: Treatment with azacytidine of patients with end-stage-β-thalassemia
-
Lowrey CH Nienhuis AW Brief report: Treatment with azacytidine of patients with end-stage- β -thalassemia N Engl J Med 329 1993 845 849
-
(1993)
N Engl J Med
, vol.329
, pp. 845-849
-
-
Lowrey, CH1
Nienhuis, AW2
-
48
-
-
0020466344
-
5-Azacytidine selectively increases gamma-globin synthesis in a patient with β+ thalassemia
-
+ thalassemia N Engl J Med 307 1982 1469 1475
-
(1982)
N Engl J Med
, vol.307
, pp. 1469-1475
-
-
Ley, TJ1
DeSimone, J2
Anagnou, NP3
-
49
-
-
0010983188
-
First report of long-term elimination of red cell transfusions in thalassemia major through augmentation of fetal hemoglobin with sodium phenylbutyrate and hydroxyurea
-
(abstr) Olivieri NF Rees DC Ginder GD First report of long-term elimination of red cell transfusions in thalassemia major through augmentation of fetal hemoglobin with sodium phenylbutyrate and hydroxyurea Blood 88 1996 310a
-
(1996)
Blood
, vol.88
, pp. 310a
-
-
Olivieri, NF1
Rees, DC2
Ginder, GD3
-
50
-
-
0025134007
-
Intact transferrin receptors in human plasma and their relation to erythropoiesis
-
Huebers HA Beguin Y Pootrakul P Intact transferrin receptors in human plasma and their relation to erythropoiesis Blood 75 1990 102 107
-
(1990)
Blood
, vol.75
, pp. 102-107
-
-
Huebers, HA1
Beguin, Y2
Pootrakul, P3
-
51
-
-
0026546708
-
The soluble transferrin receptor: biological aspects and clinical usefulness as quantitative measure of erythropoiesis
-
Beguin Y The soluble transferrin receptor: biological aspects and clinical usefulness as quantitative measure of erythropoiesis Haematologica (Pavia) 77 1992 1 10
-
(1992)
Haematologica (Pavia)
, vol.77
, pp. 1-10
-
-
Beguin, Y1
-
52
-
-
0014040265
-
Developmental and acquired variations in erythrocyte carbonic anhydrase isozymes
-
Weatherall DJ McIntyre PA Developmental and acquired variations in erythrocyte carbonic anhydrase isozymes Br J Haematol 13 1967 106 114
-
(1967)
Br J Haematol
, vol.13
, pp. 106-114
-
-
Weatherall, DJ1
McIntyre, PA2
-
53
-
-
4244213741
-
Profound increases in fetal hemoglobin during hydroxyurea and butyrate therapy are not associated with reversion to fetal erythropoiesis
-
Rees DC Thein SW Dover GJ Profound increases in fetal hemoglobin during hydroxyurea and butyrate therapy are not associated with reversion to fetal erythropoiesis Blood 88 1996 311a
-
(1996)
Blood
, vol.88
, pp. 311a
-
-
Rees, DC1
Thein, SW2
Dover, GJ3
|