Results 1 to 10 of about 1,066,030 (332)

Hemoglobin E disease and glycosylated hemoglobin

open access: yesIndian Journal of Endocrinology and Metabolism, 2015
Glycosylated hemoglobin (HbA1C) is a routinely measured parameter to monitor long-term glycemic control in people with diabetes mellitus. The presence of hemoglobin (Hb) variants can affect the accuracy of HbA1C methods.
Niharika Yedla   +2 more
doaj   +3 more sources

Agglutination Reactions of Artemisinin-Type Drugs and Other Substances [PDF]

open access: yesBIO Web of Conferences, 2023
Artemisinin is a good antimalarial drug independently developed in China. It is highly effective and low toxic. In the process of studying the antimalarial mechanism of artemisinin drugs, we found that there was agglutination when the drugs came into ...
Yan Bin   +3 more
doaj   +1 more source

Polyethylene Glycol Camouflaged Earthworm Hemoglobin. [PDF]

open access: yes, 2017
Nearly 21 million components of blood and whole blood and transfused annually in the United States, while on average only 13.6 million units of blood are donated. As the demand for Red Blood Cells (RBCs) continues to increase due to the aging population,
Cabrales, Pedro   +8 more
core   +16 more sources

Clinical effect and learning curve of endoscopic two-way catheterization on anastomotic fistula after esophageal cancer surgery

open access: yesZhongguo linchuang yanjiu, 2023
Objective To investigate the clinical effect of endoscopic two-way catheterization in the treatment of anastomotic fistula after esophageal cancer surgery. Methods From August 2017 to October 2020, 211 patients with postoperative anastomotic fistula of
YANG Yu-yu*, HUANG Wei-zhao, WU Ying-meng, DING Xin
doaj   +1 more source

Alpha‐thalassemia. Case report alpha‐thalassemia in a Costa Rican family, A case report

open access: yesClinical Case Reports, 2021
This case report highlights the importance for health care providers to be aware of the αlpha‐thalassemia syndromes, their relevance to clinical care and family counseling, appropriate diagnostic algorithm for definitive diagnosis.
Mariela Solano‐Vargas   +2 more
doaj   +1 more source

Maternal hemoglobin concentrations across pregnancy and child health and development from birth through 6–7 years

open access: yesFrontiers in Nutrition, 2023
BackgroundThe role of changes in maternal hemoglobin (Hb) across pregnancy on child health and development (CHD) remains unclear.ObjectiveWe examined the association between maternal Hb trajectories and CHD outcomes: (a) birth outcomes (birth weight ...
Melissa F. Young   +11 more
doaj   +1 more source

Acceleration of hemoglobin C crystallization by hemoglobin S [PDF]

open access: yesBlood, 1989
We previously reported that circulating hemoglobin (Hb) CC erythrocytes contain oxygenated HbC crystals with little or no HbF and that HbF inhibits in vitro crystallization of HbC. We now report that HbS accelerates in vitro crystallization of HbC. Crystals were formed in 1.8 mol/L potassium phosphate buffer, pH 7.4, at 30 degrees C and were counted in
M J, Lin, R L, Nagel, R E, Hirsch
openaire   +2 more sources

Influence of systematic training on morphophysiological and motor ability profiles of Indian young male kayakers

open access: yesIndian Journal of Health Sciences and Biomedical Research KLEU, 2023
CONTEXT: Little information is there on the training effect on junior Indian kayakers. Hence, it is of great interest to explore the influence of systematic training on morphophysiological and motor ability profiles of Indian young male kayakers.
Tamoghni Manna   +2 more
doaj   +1 more source

Hemoglobin I: An Inherited Hemoglobin Anomaly [PDF]

open access: yesBlood, 1955
Abstract A hitherto undescribed hemoglobin anomaly has been detected in a North Carolina Negro family. This new hemoglobin, designated type I, which has been electrophoretically characterized, was found in combination with normal adult A hemoglobin in 6 of 17 members of one family.
D L, RUCKNAGEL, E B, PAGE, W N, JENSEN
openaire   +2 more sources

Effects of α subunit substitutions on the oxidation of βCys93 and the stability of sickle cell hemoglobin

open access: yesRedox Report, 2020
The β subunit substitutions, F41Y and K82D, in sickle cell hemoglobin (Hb) (βE6 V) provides significant resistance to oxidative stress by shielding βCys93 from the oxidizing ferryl heme.
Wayne Hicks   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy