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]
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]
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]
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]
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]
Rodrigo Abreu Camacho +9 more
doaj +2 more sources
Hemoglobin S and C affect protein export in Plasmodium falciparum-infected erythrocytes [PDF]
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]
Nouh Al-Mahrouqi +8 more
doaj +2 more sources
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
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]
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

