Zobrazeno 1 - 10
of 1 052
pro vyhledávání: '"hemoglobin S"'
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 32, Iss , Pp 101913- (2023)
Purpose: To report two cases of symptomatic posterior pole arterial occlusions in patients with hemoglobin SS disease. Observations: Two teenage patients with hemoglobin SS disease presented with visual distortions, and on dilated fundus examination
Externí odkaz:
https://doaj.org/article/46594373a35844d29b5f4f00e16d704c
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 1, Pp 45-51 (2023)
Introduction: Sickle cell anemia is a monogenic disorder caused by a mutation in the β-hemoglobin gene, resulting in sickle hemoglobin that can polymerize. Presentation and clinical course have significant inter-individual variability and classifyin
Externí odkaz:
https://doaj.org/article/96847aeb60a64709aa988ce52ad83cc6
Akademický článek
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Akademický článek
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Publikováno v:
Practical Laboratory Medicine, Vol 34, Iss , Pp e00312- (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. We examined correlation of A1c CE results with results of CE analysis for
Externí odkaz:
https://doaj.org/article/f9ae678c42404c2cb9e781dd3cf6bd5f
Autor:
Travis Nemkov, Sarah Skinner, Mor Diaw, Saliou Diop, Abdoulaye Samb, Philippe Connes, Angelo D’Alessandro
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Subjects with sickle cell trait (SCT) carry one copy of mutated β-globin gene at position E6V at the origin of the production of sickle hemoglobin (HbS). Indeed, individuals with SCT have both normal hemoglobin and HbS, in contrast to patients with
Externí odkaz:
https://doaj.org/article/a2e6cd7caacf492482def2d1a63b57b7
Autor:
Vida Ebrahimi, Atieh Hashemi
Publikováno v:
Trends in Peptide and Protein Sciences, Vol 6, Pp 1-8 (e2) (2021)
Sickle cell diseases are the most prevalent monogenic blood diseases with complications such as severe end-organ harm, pain, and reduced life expectancy. Dealing options for sickle cell diseases are inadequate, as there are just two FDA-approved drug
Externí odkaz:
https://doaj.org/article/d97f6c20359b4a61aa22ad28a7cadb78
Autor:
Hilda J. Tutuba, Agnes Jonathan, William Lloyd, Fredrick Luoga, Emanuela Marco, Joyce Ndunguru, Benson R. Kidenya, Julie Makani, Paschal Ruggajo, Irene K. Minja, Emmanuel Balandya
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Sickle cell disease (SCD) is the single most important genetic cause of childhood mortality globally. Newborn screening (NBS) is the recommended intervention aimed at early identification of babies with SCD and their linkage to care. To e
Externí odkaz:
https://doaj.org/article/8e4477fda54d4a45b3380ee484967a75
Publikováno v:
Case Reports in Ophthalmology, Vol 11, Iss 2, Pp 189-195 (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. In this report, we present ophthalmic examination findin
Externí odkaz:
https://doaj.org/article/f62aba519f044148be69c15bf541c68a
Publikováno v:
Clinical Case Reports, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract The presented case will shed some light on one of the rarest complications of HBSE disease, which is acute chest syndrome, and will highlight the management of that complication.
Externí odkaz:
https://doaj.org/article/e863774941a3437b9933ff21b630f9af