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pro vyhledávání: '"L. M. Rabb"'
Publikováno v:
British Journal of Ophthalmology. 67:782-785
Children with homozygous sickle cell (SS) disease and with sickle cell-haemoglobin C (SC) disease, aged 6 1/2 to 8 1/2 years, were examined by fluorescein angiography/angioscopy to determine the presence of retinal nonperfusion. The haematological an
Autor:
G R Serjeant, Karlene Mason, Yvonne Grandison, L. M. Rabb, Richard J. Hayes, Beryl E. Serjeant
Publikováno v:
Scopus-Elsevier
A double blind controlled trial of supplementation with folic acid has been performed in 117 children with homozygous sickle cell (SS) disease aged 6 months to 4 years over a 1 year period. No megaloblastic change was observed in either group. At the