Beta-thalassemia

Pitfalls in genetic counselling for β-thalassemia: an individual with 4 different thalassemia mutations

(2010) R. Galanello et al.   CLINICAL GENETICS

Amelioration of Sardinian  0 thalassemia by genetic modifiers

(2009) R. Galanello et al.   BLOOD

The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

(2009) K. Wahlberg et al.   BLOOD

BCL11A represses HBG transcription in K562 cells

(2009) Zhiyi Chen et al.   BLOOD CELLS MOLECULES AND DISEASES

Long-term sequential deferiprone-deferoxamineversusdeferiprone alone for thalassaemia major patients: a randomized clinical trial

(2009) Aurelio Maggio et al.   BRITISH JOURNAL OF HAEMATOLOGY

Discovering the genetics underlying foetal haemoglobin production in adults

(2009) Swee Lay Thein et al.   BRITISH JOURNAL OF HAEMATOLOGY

Association of   globin gene quadruplication and heterozygous   thalassemia in patients with thalassemia intermedia

(2009) M. C. Sollaino et al.   HAEMATOLOGICA

Segmental duplications involving the α-globin gene cluster are causing β-thalassemia intermedia phenotypes in β-thalassemia heterozygous patients

(2008) C.L. Harteveld et al.   BLOOD CELLS MOLECULES AND DISEASES

BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies

(2008) Amanda E. Sedgewick et al.   BLOOD CELLS MOLECULES AND DISEASES

Onset of cardiac iron loading in pediatric patients with thalassemia major

(2008) J. C. Wood et al.   HAEMATOLOGICA

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of  -thalassemia

(2008) M. Uda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

DNA polymorphisms at the BCL11A, HBS1L-MYB, and  -globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

(2008) G. Lettre et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific RepressorBCL11A

(2008) Vijay G. Sankaran et al.   SCIENCE

Once-daily oral deferasirox for the treatment of transfusional iron overload

(2008) Renzo Galanello et al.   Expert Review of Clinical Pharmacology