Results 1 to 10 of about 731,911 (182)

Compound heterozygosity for hemoglobin S and hemoglobin E in a family of Proto-Australoid origin: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2021
Background Hemoglobin S and E are commonly occurring hemoglobin variants among distinctly separate tribal populations of Central and Northeast India, respectively.
Noymi Basumatary   +3 more
doaj   +2 more sources

Hemoglobin S identification in blood donors: A cross section of prevalence [PDF]

open access: yesHematology, Transfusion and Cell Therapy, 2022
Introduction: In Brazil, the sickle cell trait (SCT) has an average prevalence of 4% in the general population and 6–10% among Afro-descendants. Although SCT is highly prevalent, a large segment of the population ignores their status.
Fernanda Lima Kroger   +5 more
doaj   +2 more sources

Hemoglobin S/OArab: Retinal Manifestations of a Rare Hemoglobinopathy [PDF]

open access: yesCase Reports in Ophthalmology, 2020
Hemoglobin S/OArab (Hgb S/OArab) disease is a rare hemoglobinopathy which presents similarly to sickle cell retinopathy, with only three prior reports that describe associated retinal findings.
Riley Sanders   +5 more
doaj   +2 more sources

Scope and efficiency of the newborn screening program in identifying hemoglobin S [PDF]

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2014
Background: In 2001, the Brazilian Ministry of Health added hemoglobinopathies to the National Neonatal Screening Program to be implemented in three steps.
Maria Lucia Ivo   +5 more
doaj   +2 more sources

PB2523: DI-2-ETHYLHEXYL PHTHALATE (DEHP) INHIBITS HEMOGLOBIN S POLYMERIZATION [PDF]

open access: yesHemaSphere, 2023
Rodrigo Abreu Camacho   +9 more
doaj   +2 more sources

Hemoglobin S and C affect protein export in Plasmodium falciparum-infected erythrocytes [PDF]

open access: yesBiology Open, 2015
Malaria is a potentially deadly disease. However, not every infected person develops severe symptoms. Some people are protected by naturally occurring mechanisms that frequently involve inheritable modifications in their hemoglobin.
Nicole Kilian   +8 more
doaj   +2 more sources

PB2521: STUDY OF HEMOGLOBIN S-OMAN TRAIT: NEW INSIGHTS [PDF]

open access: yesHemaSphere, 2023
Nouh Al-Mahrouqi   +8 more
doaj   +2 more sources

Frequency of carrier state of thalassemia and various hemoglobinopathies in tertiary care hospital of Pakistan.

open access: yesInternational Journal of Endorsing Health Science Research, 2021
Background: It has been estimated that 5% of the global population are carriers of Hemoglobin (Hb) disorders. These disorders may cause hemolytic anemia leading to the critical condition of the patients.
Saba Kamil   +7 more
doaj   +1 more source

Quantitation of hemoglobins using Sebia Capillarys-2 capillary electrophoresis (CE) for A1c: Comparison to results using CE for hemoglobins

open access: yesPractical Laboratory Medicine, 2023
Background: Measurement of A1c using the Sebia Capillarys-2 capillary electrophoresis (A1c CE) involves relative quantitative measurements of peaks for hemoglobins A1c, A, A2.
Catherine M. Tucker, Douglas F. Stickle
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

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