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Predicting clinical severity in sickle cell anaemia

British journal of haematology, 2005-05, Vol.129 (4), p.465-481

Steinberg, M. H.

2005

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Management of Sickle Cell Disease

The New England journal of medicine, 1999-04, Vol.340 (13), p.1021-1030

1999

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Clinical and Radiologic Findings of Inner Ear Involvement in Sickle Cell Disease

American journal of neuroradiology : AJNR, 2011-12, Vol.32 (11), p.2160-2164

2011

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Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

The New England journal of medicine, 1994-06, Vol.330 (23), p.1639-1644

1994

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BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Blood cells, molecules, & diseases, 2015-03, Vol.54 (3), p.224-230

2015

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Quantitative MRI analysis of craniofacial bone marrow in patients with sickle cell disease

American journal of neuroradiology : AJNR, 2013-03, Vol.34 (3), p.622-627

2013

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Dominantly inherited β thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the β globin gene: Hb morgantown (β91 CTG>CG)

Journal of clinical pathology, 2005-10, Vol.58 (10), p.1110-1112

2005

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CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia

The New England journal of medicine, 2021-01, Vol.384 (3), p.252-260

2021

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Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

The pharmacogenomics journal, 2007-12, Vol.7 (6), p.386-394

2007

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Mutations in the β-globin gene from a Saudi population: an update

International journal of laboratory hematology, 2016-04, Vol.38 (2), p.e38-e40

2016

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Determinants of fetal hemoglobin response to hydroxyurea

Seminars in hematology, 1997-07, Vol.34 (3), p.8-14

STEINBERG, M. H

1997

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Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia

Cellular and molecular biology (Noisy-le-Grand, France), 2004-02, Vol.50 (1), p.23

2004

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Collagen-Platelet Interactions: Evidence for a Direct Interaction of Collagen With Platelet GPIa/IIa and an Indirect Interaction With Platelet GPIIb/IIIa Mediated by Adhesive Proteins

Blood, 1989-07, Vol.74 (1), p.182-192

1989

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Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia

American journal of hematology, 1995-03, Vol.48 (3), p.175-181

1995

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Hemoglobin A2: Origin, Evolution, and Aftermath

Blood, 1991-11, Vol.78 (9), p.2165-2177

1991

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Exagamglogene Autotemcel for Severe Sickle Cell Disease

The New England journal of medicine, 2024-05, Vol.390 (18), p.1649-1662

2024

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Effectiveness of a dedicated day hospital for management of acute sickle cell pain

Haematologica (Roma), 2007-06, Vol.92 (6), p.854-854

2007

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Sexually transmitted diseases in South Africa

Genitourinary Medicine, 1996-06, Vol.72 (3), p.160-171

1996

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Cellular effects of hydroxyurea in Hb SC disease

British journal of haematology, 1997-09, Vol.98 (4), p.838-844

1997

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α-Thalassemia in Blacks: Genetic and Clinical Aspects and Interactions With the Sickle Hemoglobin Gene

Blood, 1986-11, Vol.68 (5), p.985-990

1986

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Disturbance of plasma and platelet thrombospondin levels in sickle cell disease

American journal of hematology, 1996-04, Vol.51 (4), p.296-301

1996

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Supplemental vitamin B and progression to AIDS and death in black South African patients infected with HIV

Journal of acquired immune deficiency syndromes (1999), 1999-07, Vol.21 (3), p.252

1999

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Hematological effects of atypical and cameroon β‐globin gene haplotypes in adult sickle cell anemia

American journal of hematology, 1998-10, Vol.59 (2), p.121-126

1998

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MODULATION OF FETAL HEMOGLOBIN IN SICKLE CELL ANEMIA

Hemoglobin, 2001-01, Vol.25 (2), p.195-211

Steinberg, Martin H.

2001

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Pharmacologic modulation of fetal hemoglobin

Medicine (Baltimore), 2001-09, Vol.80 (5), p.328-344

2001

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Predicting clinical severity in sickle cell anaemia

Management of Sickle Cell Disease

Clinical and Radiologic Findings of Inner Ear Involvement in Sickle Cell Disease

Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia

Quantitative MRI analysis of craniofacial bone marrow in patients with sickle cell disease

Dominantly inherited β thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the β globin gene: Hb morgantown (β91 CTG>CG)

CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea

Mutations in the β-globin gene from a Saudi population: an update

Determinants of fetal hemoglobin response to hydroxyurea

Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia

Collagen-Platelet Interactions: Evidence for a Direct Interaction of Collagen With Platelet GPIa/IIa and an Indirect Interaction With Platelet GPIIb/IIIa Mediated by Adhesive Proteins

Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia

Hemoglobin A2: Origin, Evolution, and Aftermath

Exagamglogene Autotemcel for Severe Sickle Cell Disease

Effectiveness of a dedicated day hospital for management of acute sickle cell pain

Sexually transmitted diseases in South Africa

Cellular effects of hydroxyurea in Hb SC disease

α-Thalassemia in Blacks: Genetic and Clinical Aspects and Interactions With the Sickle Hemoglobin Gene

Disturbance of plasma and platelet thrombospondin levels in sickle cell disease

Supplemental vitamin B and progression to AIDS and death in black South African patients infected with HIV

Hematological effects of atypical and cameroon β‐globin gene haplotypes in adult sickle cell anemia

MODULATION OF FETAL HEMOGLOBIN IN SICKLE CELL ANEMIA

Pharmacologic modulation of fetal hemoglobin

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