Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell trait.

A defect in urine concentrating ability occurs in individuals with sickle cell trait (HbAS). This may result from intracellular polymerization of sickle hemoglobin (HbS) in erythrocytes, leading to microvascular occlusion, in the vasa recta of the renal medulla. To test the hypothesis that the sever...

Ful tanımlama

Detaylı Bibliyografya

Yayımlandı:	J Clin Invest
Asıl Yazarlar:	Gupta, A K, Kirchner, K A, Nicholson, R, Adams, J G, Schechter, A N, Noguchi, C T, Steinberg, M H
Materyal Türü:	Artigo
Dil:	Inglês
Baskı/Yayın Bilgisi:	American Society for Clinical Investigation 1991
Konular:	Research Article
Online Erişim:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC295777/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1752955/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115521
Etiketler:	Etiketle Etiket eklenmemiş, İlk siz ekleyin!