A. J. Bellingham

Medicine · Health Sciences

30h-index2.6kcitations112works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(41), Erythrocyte Function and Pathophysiology(28), Neonatal Health and Biochemistry(21), Hemoglobin structure and function(16), Blood groups and transfusion(11)

Publications112 total

Thesickling processinrelation toclinical manifestations
2017
Intravenous oxpentifylline and the painful crisis of sickle cell disease
Clinical Hemorheology and Microcirculation·2016· 7 cited
Neonatal screening for haemoglobin variants using filter paper-dried blood specimens
Clinical & Laboratory Haematology·2008· 13 cited
Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells
Blood·1999· 1 cited
Reversal of Metabolic Block in Glycolysis by Enzyme Replacement in Triosephosphate Isomerase–Deficient Cells
Blood·1999· 25 cited
Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal
Biomedical Chromatography·1998· 21 cited
Metabolic Correction of Triose Phosphate Isomerase Deficiencyin Vitroby Complementation
Biochemical and Biophysical Research Communications·1997· 11 cited
Evidence for founder effect of the glu104asp substitution and identification of new mutations in triosephosphate isomerase deficiency
Human Mutation·1997· 1 cited
Hydroxyurea, Sickle Cell Disease and Renal Transplantation
Nephron·1997· 12 citedOpen Access
Evidence for founder effect of the glu104asp substitution and identification of new mutations in triosephosphate isomerase deficiency
Human Mutation·1997· 49 cited
Tucaresol increases oxygen affinity and reduces haemolysis in subjects with sickle cell anaemia
British Journal of Haematology·1996· 53 cited
Guidelines for the clinical use of blood cell separators
Clinical & Laboratory Haematology·1996
Managing patients with an absent or dysfunctional spleen: Guidelines should highlight risk of salmonella infection in sickle cell disease
BMJ·1996· 8 citedOpen Access
Emergence of ciprofloxacin resistance during treatment of salmonella osteomyelitis in three patients with sickle cell disease
Journal of Infection·1996· 22 cited
Hereditary red cell enzymopathies
Blood Reviews·1995· 24 cited
Screening for ophthalmic manifestations of sickle cell disease in the United Kingdom
Eye·1994· 27 citedOpen Access
Salmonella bacteraemia in sickle cell disease at King's College Hospital: 1976–1991
Journal of Hospital Infection·1994· 18 cited
DNA sequence abnormalities in human glucose 6-phosphate isomerase deficiency
Human Molecular Genetics·1993· 31 cited
Neonatal Screening for Sickle Cell Disease in London Neonates
Palgrave Macmillan UK eBooks·1992
Current problems in haematology. 2: Hereditary spherocytosis.
Journal of Clinical Pathology·1991· 8 citedOpen Access
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Frequent Co-authors

D. Mark Layton(6), Roopen Arya(5), Claude Lenfant(4), E. R. Huehns(4), John P. Keenan(4), G. P. Summerfield(3), A. D. Stephens(3), M Brozović(3), Humphrey Pullon(3), J C Detter(2), M E Horn(2), Moira Dick(2), C Bunch(2), M. R. A. LALLOZ(2), G. W. Marsh(2), Nicki-Jayne Russell(2), Robin Ireland(2), Giorgio Senaldi(2), Kiran Veerapan(2), Diego Vergani(2)