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Alpha thalassaemia and the macular vasculature in homozygous sickle cell disease.

The interaction of homozygous alpha thalassaemia 2 with homozygous sickle cell (SS) disease results in a generally milder haematological picture with less intravascular sickling, less haemolysis, and higher haemoglobin levels. Clinically, patients are generally more mildly affected, though not all v...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Condon, P I, Marsh, R J, Maude, G H, Higgs, D R, Weatherall, D J, Serjeant, G R
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 1983
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC1040198/
https://ncbi.nlm.nih.gov/pubmed/6639911
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