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Journal Articles

Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia

I Dianzani, E Garelli, C Dompe, N Crescenzio, F Locatelli, G Schiliro, G Castaman, GP Bagnara, NF Olivieri, V Gabutti, U Ramenghi

Blood (1996) 87 (6): 2568–2572.

https://doi.org/10.1182/blood.V87.6.2568.bloodjournal8762568

Published: 1996

Journal Articles

Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo

O Shalev, T Repka, A Goldfarb, L Grinberg, A Abrahamov, NF Olivieri, EA Rachmilewitz, RP Hebbel

Blood (1995) 86 (5): 2008–2013.

https://doi.org/10.1182/blood.V86.5.2008.bloodjournal8652008

Published: 1995

Journal Articles

Rapid healing of chronic leg ulcers during arginine butyrate therapy in patients with sickle cell disease and thalassemia [letter]

GD Sher, NF Olivieri

Blood (1994) 84 (7): 2378–2380.

https://doi.org/10.1182/blood.V84.7.2378.2378

Published: 1994

Journal Articles

Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]

JS Waye, B Eng, M Patterson, DH Chui, NF Olivieri

Blood (1994) 83 (11): 3418–3420.

https://doi.org/10.1182/blood.V83.11.3418.3418

Published: 1994

Journal Articles

Failure of recombinant human interleukin-3 therapy to induce erythropoiesis in patients with refractory Diamond-Blackfan anemia [see comments]

NF Olivieri, SA Feig, L Valentino, AM Berriman, R Shore, MH Freedman

Blood (1994) 83 (9): 2444–2450.

https://doi.org/10.1182/blood.V83.9.2444.2444

Published: 1994

Journal Articles

Iron-balance and dose-response studies of the oral iron chelator 1,2- dimethyl-3-hydroxypyrid-4-one (L1) in iron-loaded patients with sickle cell disease

AF Collins, FF Fassos, S Stobie, N Lewis, D Shaw, M Fry, DM Templeton, RA McClelland, G Koren, NF Olivieri

Blood (1994) 83 (8): 2329–2333.

https://doi.org/10.1182/blood.V83.8.2329.2329

Published: 1994

Journal Articles

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

NF Olivieri, MH Freedman, SP Perrine, GJ Dover, B Sheridan, DL Essentine, RL Nagel

Blood (1992) 80 (12): 3258–3260.

https://doi.org/10.1182/blood.V80.12.3258.3258

Published: 1992

Journal Articles

Reduction of tissue iron stores and normalization of serum ferritin during treatment with the oral iron chelator L1 in thalassemia intermedia

NF Olivieri, G Koren, D Matsui, PP Liu, L Blendis, R Cameron, RA McClelland, DM Templeton

Blood (1992) 79 (10): 2741–2748.

https://doi.org/10.1182/blood.V79.10.2741.2741

Published: 1992

Journal Articles

Influence of steel factor on hemoglobin synthesis in sickle cell disease

BA Miller, SP Perrine, A Bernstein, SD Lyman, DE Williams, LL Bell, NF Olivieri

Blood (1992) 79 (7): 1861–1868.

https://doi.org/10.1182/blood.V79.7.1861.1861

Published: 1992

Journal Articles

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments]

SP Cai, B Eng, WH Francombe, NF Olivieri, AG Kendall, JS Waye, DH Chui

Blood (1992) 79 (5): 1342–1346.

https://doi.org/10.1182/blood.V79.5.1342.1342

Published: 1992

Journal Articles

Diamond-Blackfan anemia: heterogenous response of hematopoietic progenitor cells in vitro to the protein product of the steel locus

NF Olivieri, T Grunberger, Y Ben-David, J Ng, DE Williams, S Lyman, DM Anderson, AA Axelrad, P Correa, A Bernstein

Blood (1991) 78 (9): 2211–2215.

https://doi.org/10.1182/blood.V78.9.2211.2211

Published: 1991

Journal Articles

An alpha-globin gene initiation codon mutation in a black family with HbH disease

NF Olivieri, LS Chang, AO Poon, AM Michelson, SH Orkin

Blood (1987) 70 (3): 729–732.

https://doi.org/10.1182/blood.V70.3.729.729

Published: 1987

NARROW

Mutations in the erythropoietin receptor gene are not a common cause of Diamond-Blackfan anemia

Deferiprone (L1) chelates pathologic iron deposits from membranes of intact thalassemic and sickle red blood cells both in vitro and in vivo

Rapid healing of chronic leg ulcers during arginine butyrate therapy in patients with sickle cell disease and thalassemia [letter]

Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]

Failure of recombinant human interleukin-3 therapy to induce erythropoiesis in patients with refractory Diamond-Blackfan anemia [see comments]

Iron-balance and dose-response studies of the oral iron chelator 1,2- dimethyl-3-hydroxypyrid-4-one (L1) in iron-loaded patients with sickle cell disease

Trial of recombinant human erythropoietin: three patients with thalassemia intermedia [letter]

Reduction of tissue iron stores and normalization of serum ferritin during treatment with the oral iron chelator L1 in thalassemia intermedia

Influence of steel factor on hemoglobin synthesis in sickle cell disease

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments]

Diamond-Blackfan anemia: heterogenous response of hematopoietic progenitor cells in vitro to the protein product of the steel locus

An alpha-globin gene initiation codon mutation in a black family with HbH disease

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American Society of Hematology

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American Society of Hematology

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