S. Vaidya

The Development of Haematological Changes in Homozygous Sickle Cell Disease: a Cohort Study from Birth to 6 Years

G. Serjeant, K. Mason, B. Serjeant, 1981, British journal of haematology.

Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood.

M. Stevens, G. Serjeant, R. Hayes, 1981, The Journal of pediatrics.

Splenic opacification in homozygous sickle cell disease.

I. McCall, G. Serjeant, S. Vaidya, 1981, Clinical radiology.

Haematological indices in normal negro children: a Jamaican cohort from birth to five years.

G. Serjeant, K. Mason, B. Serjeant, 1980, Clinical and laboratory haematology.

Serum immunoglobulin levels in children with homozygous sickle cell disease.

G. Serjeant, K. De Ceulaer, S. Vaidya, 1982, Clinica chimica acta; international journal of clinical chemistry.

Pneumococcal and other infections in children with sickle-cell hemoglobin C (SC) disease.

G. Serjeant, R. Hayes, J. Topley, 1982, The Journal of pediatrics.

EARLY SPLENOMEGALY IN HOMOZYGOUS SICKLE-CELL DISEASE: AN INDICATOR OF SUSCEPTIBILITY TO INFECTION

G. Serjeant, D. Rogers, S. Vaidya, 1978, The Lancet.