S. Davies

发表

Fetal haemoglobin augmentation in E/β0 thalassaemia: clinical and haematological outcome

D. Weatherall, E. Vichinsky, N. Olivieri, 2005, British journal of haematology.

Therapeutic challenges in childhood sickle cell disease Part 1: current and future treatment options

P. Amrolia, I. Roberts, C. Halsey, 2003, British journal of haematology.

Single and Combination Drug Therapy for Fetal Hemoglobin Augmentation in Hemoglobin E‐β0‐Thalassemia: Considerations for Treatment

D. Weatherall, E. Vichinsky, N. Olivieri, 2005, Annals of the New York Academy of Sciences.

Clinical Aspects of Paediatric Blood Transfusion: Cellular Components

S. Davies, S. Kinsey, S. Kinsey, 1994, Vox sanguinis.

Impact of bone marrow transplantation for symptomatic sickle cell disease: an interim report. Multicenter investigation of bone marrow transplantation for sickle cell disease.

C. Pegelow, J. Scott, K. Sullivan, 2000, Blood.

Bone marrow transplantation for sickle cell disease.

J. Scott, K. Sullivan, R. Storb, 1996, The New England journal of medicine.

Bone marrow transplantation for sickle cell disease.

S. Davies, S C Davies, S. Davies, 1993, Archives of disease in childhood.

Psychological adjustment and family functioning in a group of British children with sickle cell disease: preliminary empirical findings and a meta-analysis.

C. McManus, S. Davies, K. Midence, 1996, The British journal of clinical psychology.

Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic‐specific rates

M. Hickman, S. Davies, B. Modell, 1999, British journal of haematology.

Psychosocial aspects of sickle cell disease (SCD) in childhood and adolescence: a review.

K. Midence, P. Fuggle, S. Davies, 1993, The British journal of clinical psychology.