B. Modell

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Psychosocial and clinical burden of thalassaemia intermedia and its implications for prenatal diagnosis.

D. Skuse, A. Yardumian, J. Porter, 1995, Archives of disease in childhood.

Hereditary anaemias and iron deficiency in a tribal population (the Baiga) of central India

M. Petrou, P. Reddy, B. Modell, 1995, European journal of haematology.

The Clinical Approach to Thalassaemia

B. Modell, V. Berdoukas, B. Modell, 1984 .

Psychological and sociological aspects of the thalassemias.

S. Ratip, B. Modell, 1996, Seminars in hematology.

Deferasirox for the treatment of iron overload associated with regular blood transfusions (transfusional haemosiderosis) in patients suffering with chronic anaemia: a systematic review and economic evaluation.

T. Walley, J. Kirkham, N. Fleeman, 2009, Health technology assessment.

Advances in the use of iron-chelating agents for the treatment of iron overload.

B. Modell, 1979, Progress in hematology.

Survival and desferrioxamine in thalassaemia major.

R. Peto, D. Weatherall, D. Flynn, 1982, British medical journal.

Total management of thalassaemia major.

B. Modell, 1977, Archives of disease in childhood.

Antenatal diagnosis of thalassaemia major.

J. Clegg, D. Weatherall, B. Alter, 1978, British medical journal.

Transfusion requirements and effects in patients with thalassaemia major

P. Rebulla, B. Modell, 1991, The Lancet.

Lifetime treatment costs of beta-thalassaemia major.

J. Karnon, A. Ades, J. Brown, 1999, Clinical and laboratory haematology.

Relationship between the severity of β‐thalassaemia syndromes and the number of alleviating mutations

M. Petrou, J. Old, J. Porter, 1997, European journal of haematology.

MANAGEMENT OF THALASSEMIA MAJOR

B. Modell, 1976 .

Beta thalassemia: an immunologic therapy?

L. Brent, L. S. Rayfield, B. Modell, 1982, Transplantation proceedings.

Chorionic villus sampling in a high‐risk population— 4 years' experience

M. Petrou, D. Maxwell, J. Hooker, 1988, British journal of obstetrics and gynaecology.

Feasibility of First Trimester Diagnosis of β-Thalassaemia Using DNA Polymorphisms in the Cypriot Population

D. Weatherall, M. Petrou, A. Fitches, 1985 .

DIRECT GENE ANALYSIS OF CHORIONIC VILLI: A POSSIBLE TECHNIQUE FOR FIRST-TRIMESTER ANTENATAL DIAGNOSIS OF HAEMOGLOBINOPATHIES

R. Williamson, J. Eskdale, D. Coleman, 1981, The Lancet.

Total management of thalassaemia major.

B. Modell, B. MODELLt, 1977, Archives of disease in childhood.