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Linkage of β -thalassaemia mutations and β -globin gene polymorphisms with DNA polymorphisms in human β -globin gene cluster

Nature (London), 1982-04, Vol.296 (5858), p.627-631

1982

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Nonrandom Association of Polymorphic Restriction Sites in the β -globin Gene Cluster

Proceedings of the National Academy of Sciences - PNAS, 1982-01, Vol.79 (1), p.137-141

1982

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β -thalassemia in Chinese: Use of in vivo RNA Analysis and Oligonucleotide Hybridization in Systematic Characterization of Molecular Defects

Proceedings of the National Academy of Sciences - PNAS, 1984-05, Vol.81 (9), p.2821-2825

1984

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ATA box transcription mutation in β-thalassemia

Nucleic acids research, 1983-07, Vol.11 (14), p.4727-4734

1983

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Iron Chelator Therapy

Oncology & Hematology Review (US), 2007 (2), p.24

Giardina, Patricia JV

2007

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A Psychosocial Needs Assessment of Patients with Homozygous β-Thalassemia

Annals of the New York Academy of Sciences, 1985-01, Vol.445 (1), p.316-323

1985

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A Psychosocial Needs Assessment of Patients with Homozygous β‐Thalassemiaa

Annals of the New York Academy of Sciences, 1985-06, Vol.445 (1), p.316-323

1985

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The Effect of Subcutaneous Deferoxamine on the Cardiac Profile of Thalassemia Major: A Five-Year Study

Annals of the New York Academy of Sciences, 1985-06, Vol.445 (1), p.282-292

1985

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Use of Oligonucleotide Hybridization in the Characterization of a β°-Thalassemia Gene (β37 TGG→TGA) in a Saudi Arabian Family

Blood, 1986-04, Vol.67 (4), p.1185-1188

1986

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731 PRENATAL DIAGNOSIS OF β-THALASSEMIA BY AMNIO-CENTESIS

Pediatric research, 1981-04, Vol.15, p.564-564

1981

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Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

American journal of hematology, 2011-01, Vol.86 (1), p.92-95

2011

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Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia

Blood, 2008-08, Vol.112 (3), p.875-885

2008

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Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension

Haematologica (Roma), 2013-09, Vol.98 (9), p.1359-1367

2013

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Editors' Acknowledgments

Animal behaviour, 2018-12, Vol.146, p.181-183

2018

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Long-Term Generation of Colony-Forming Cells in Liquid Culture of CD34+ Cord Blood Cells in the Presence of Recombinant Human Stem Cell Factor

Blood, 1992-05, Vol.79 (10), p.2620-2627

1992

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Effects of recombinant human stem cell factor (SCF) on the growth of human progenitor cells in vitro

Journal of cellular physiology, 1991-09, Vol.148 (3), p.503-509

1991

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The changing profile of homozygous beta-thalassemia: demography, ethnicity, and age distribution of current North American patients and changes in two decades

Pediatrics (Evanston), 1996-03, Vol.97 (3), p.352-356

1996

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Iron Chelation with Oral Deferiprone in Patients with Thalassemia

The New England journal of medicine, 1998-12, Vol.339 (23), p.1710-1714

1998

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β-Thalassemia Due to Two Novel Nucleotide Substitutions in Consensus Acceptor Splice Sequences of the β-Globin Gene

Blood, 1989-03, Vol.73 (4), p.914-918

1989

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Linkage of β -thalassaemia mutations and β -globin gene polymorphisms with DNA polymorphisms in human β -globin gene cluster

Nonrandom Association of Polymorphic Restriction Sites in the β -globin Gene Cluster

β -thalassemia in Chinese: Use of in vivo RNA Analysis and Oligonucleotide Hybridization in Systematic Characterization of Molecular Defects

ATA box transcription mutation in β-thalassemia

Iron Chelator Therapy

A Psychosocial Needs Assessment of Patients with Homozygous β-Thalassemia

A Psychosocial Needs Assessment of Patients with Homozygous β‐Thalassemiaa

The Effect of Subcutaneous Deferoxamine on the Cardiac Profile of Thalassemia Major: A Five-Year Study

Use of Oligonucleotide Hybridization in the Characterization of a β°-Thalassemia Gene (β37 TGG→TGA) in a Saudi Arabian Family

731 PRENATAL DIAGNOSIS OF β-THALASSEMIA BY AMNIO-CENTESIS

Quality of life in thalassemia: A comparison of SF‐36 results from the thalassemia longitudinal cohort to reported literature and the US norms

Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia

Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension

Editors' Acknowledgments

Long-Term Generation of Colony-Forming Cells in Liquid Culture of CD34+ Cord Blood Cells in the Presence of Recombinant Human Stem Cell Factor

Effects of recombinant human stem cell factor (SCF) on the growth of human progenitor cells in vitro

The changing profile of homozygous beta-thalassemia: demography, ethnicity, and age distribution of current North American patients and changes in two decades

Iron Chelation with Oral Deferiprone in Patients with Thalassemia

β-Thalassemia Due to Two Novel Nucleotide Substitutions in Consensus Acceptor Splice Sequences of the β-Globin Gene

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