Results 161 to 170 of about 39,321 (195)

Erythropoietin Levels in Heterozygous Alpha-Thalassemia

Acta Haematologica, 1986
In guinea pig bone marrow cultures with heterozygous alpha-thalassemic serum, 59Fe uptake values are elevated above iron values of cultures with serum of normal subjects. These results show that erythropoietin (EP) activity values in heterozygous alpha-thalassemia are comparable to those previously observed by ourselves in heterozygous beta-thalassemia
M, Vedovato, G, Salvatorelli, G C, Balboni, M, Taddei Masieri, B, Dolcini, C, Toffoli   +5 more
openaire   +2 more sources

Intrauterine therapy for homozygous $alpha;-thalassemia

Obstetrics & Gynecology, 1995
Alpha-thalassemia is one of the most common genetic disorders in the world and is becoming more common in the United States with the increase in immigration of susceptible populations. This disease has been stated previously to be incompatible with extrauterine life.A Filipino woman with a prior loss due to hemoglobin Bart's underwent prenatal ...
S, Carr, L, Rubin, D, Dixon, J, Star, J, Dailey   +4 more
openaire   +2 more sources

Alpha and beta thalassemia.

American family physician, 2009
The thalassemias are a group of inherited hematologic disorders caused by defects in the synthesis of one or more of the hemoglobin chains. Alpha thalassemia is caused by reduced or absent synthesis of alpha globin chains, and beta thalassemia is caused by reduced or absent synthesis of beta globin chains.
Herbert L, Muncie, James, Campbell
openaire   +1 more source

Alpha-thalassemia in Thailand.

Hemoglobin, 1989
The alpha-thalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of alpha-chain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb Bart's hydrops fetalis syndrome.
P, Winichagoon, V, Thonglairuam, S, Fucharoen, V S, Tanphaichito, P, Wasi   +4 more
openaire   +1 more source

Alpha‐Thalassemia

2004
Renzo Galanello, Antonio Cao
openaire   +2 more sources

Alpha Chain Thalassemia in Taiwan

Clinical Pediatrics, 1977
K, Lin, C, Liu, T, Lee, R Q, Blackwell, J T, Huang   +4 more
openaire   +2 more sources

Alpha-Thalassemia

2021
openaire   +1 more source

The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease

New England Journal of Medicine, 1982
Douglas R Higgs
exaly  

Alpha-thalassemia.

Current topics in hematology, 1983
D R, Higgs, D J, Weatherall
openaire   +1 more source

Alpha Chain Thalassemia

Clinical Pediatrics, 1977
openaire   +1 more source