Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG). 来自 国家科技图书文献中心 喜欢 0 阅读量: 134 作者:B Eng,L Walker,JS Waye 摘要:We report a new alpha-thalassemia (alpha-thal) point mutation detected in a woman with alpha(+)-thal ...
Alpha thalassemia traitmasquerading as hemoglobin H disease due to co - existing primarymyelofibrosis[J]. Annals of hematology,2015 ,94(5) :875.Chi-Chiu, SoAmy Y., ChanJoyce C., ChanEdmond S., Ma. (2015) Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing ...
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype View further author informationhttps://orcid.org/0000-0002-1009-7649deepakbansaldr@gmail.comDeepak BansalView further author informationJasbir Kaur HiraView ...
The level of Hb C in the erythrocytes of individuals with Hb C trait decreases significantly in the presence of coexisting alpha-thalassemia. This relationship may result from the higher affinity of beta A than beta C for limiting amounts of alpha-globin during hemoglobin assembly. This mechanism...
Aim: To identify the optimal cutoff of mean corpuscular volume (MCV) for screening of alpha-thalassemia 1 trait. Methods: The database of pregnant women who attended antenatal care clinic at Department of Obstetrics and Gynecology, Chiang Mai University during January 1st, 2015 to December 31st,...
Previous studies have shown that subjects with sickle cell trait (SCT), alpha-thalassemia (alpha-t), and the dual hemoglobinopathy (SCT/alpha-t) manifest subtle, albeit significant, differences during exercise. To better understand such differences, we assessed skeletal muscle histomorphological and ...
This type of hemoglobinopathy produces a group of disorders known as the thalassemia syndromes; as in those with sickle cell trait, thalassemia is believed to provide partial protection from malaria and occurs in high prevalence in the Mediterranean area, the Middle East, and southeast Asia. More ...
Confirmation of the validity of using birth MCV for the diagnosis of alpha thalassemia trait.doi:10.4081/hr.2009.e20HbBartshighperformanceliquidchromatographyMCHMCVThirty-four blood samples of neonates in Dubai, UAE, with an MCV below 90 fL were checked by high performance liquid chromatography (...
The Coulter Counter model S-Plus measures the erythrocyte, leukocyte, and platelet counts, and the mean cell volume of erythrocytes and platelets. Two addi... Bessman,J David - 《American Journal of Clinical Pathology》 被引量: 121发表: 1980年 Prevalence of beta-thalassemia trait in premarital...
alpha-Thalassemiabeta-Globinsnitric oxide synthase type IIIhemoglobinsnitric oxidesickle cell traitSevere malaria is associated with impaired nitric oxide (NO) synthase (NOS)鈥揹ependent vasodilation, and reversal of this deficit improves survival in murine models. Malaria might have selected for ...