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Influence of alpha thalassaemia on the retinopathy of homozygous sickle cell disease.

Homozygous alpha+ thalassaemia (alpha-/alpha-) ameliorates some of the clinical manifestations of homozygous sickle cell (SS) disease but its effect on retinal complications remains unknown. This has been assessed by visual examination and fluorescein angiography in 39 subjects with SS disease and h...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Br J Ophthalmol
Asıl Yazarlar: Fox, P D, Higgs, D R, Serjeant, G R
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Publishing Group 1993
Konular:
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC504436/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8435425/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/bjo.77.2.89
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