Results 1 to 10 of about 21,951,469 (257)
Compound heterozygosity for hemoglobin S and hemoglobin E in a family of Proto-Australoid origin: a case report [PDF]
Journal 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
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Hemoglobin S identification in blood donors: A cross section of prevalence [PDF]
Hematology, 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
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Hemoglobin S/OArab: Retinal Manifestations of a Rare Hemoglobinopathy [PDF]
Case 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
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Scope and efficiency of the newborn screening program in identifying hemoglobin S [PDF]
Revista 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]
HemaSphere, 2023 Rodrigo Abreu Camacho +9 more
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Hemoglobin S and C affect protein export in Plasmodium falciparum-infected erythrocytes [PDF]
Biology 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
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PB2521: STUDY OF HEMOGLOBIN S-OMAN TRAIT: NEW INSIGHTS [PDF]
HemaSphere, 2023 Nouh Al-Mahrouqi +8 more
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International 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
Practical 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
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A clinico-hematological study of sickle cell disease among adult patients in Makkah, Saudi Arabia. [PDF]
Al-Azhar International Medical Journal, 2023 Background: Sickle cell disease is an autosomal recessive disease characterized by aberrant production of hemoglobin S (HbS). The clinical picture includes hemolytic anemia, vascular occlusion events, acute and persistent pain, and varied organ damage ...
Ahmad Arbaeen
doaj +1 more source