Fatal bone marrow embolism in a patient with sickle cell beta + thalassaemia.

Sickle cell beta + thalassaemia is regarded as the mildest of the sickle cell haemoglobinopathy syndromes with a benign natural course. In contrast to sickle cell disease, severe life threatening complications are not usually associated with this genotype. A case of a 30 year old West Indian man who...

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Detaylı Bibliyografya
Asıl Yazarlar: Zaidi, Y, Sivakumaran, M, Graham, C, Hutchinson, R M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1996
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC500734/
https://ncbi.nlm.nih.gov/pubmed/9038769
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