Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Elevated HbF"'
Autor:
Wan Suriana Wan Ab Rahman, Wan Zaidah Abdullah, Zefarina Zulkafli, Rozieyati Mohamed Saleh, Maryam Azlan, Siti Nor Assyuhada Mat Ghani, Mohd Nazri Hassan
Publikováno v:
Asia Pacific Journal of Molecular Biology and Biotechnology. :10-18
Mutations in the β-globin gene cluster can lead to β-thalassaemia, δβ-thalassaemia, hereditary persistence of foetal haemoglobin (HPFH) and some of the haemoglobin variants. The clinical and haematological spectrum of thalassaemia range from beni
Autor:
Priya Hariharan, Anita Nadkarni
Publikováno v:
Blood reviews. 49
The clinical heterogeneity of β-hemoglobinopathies is so variable that it prompted the researchers to identify the genetic modulators of these diseases. Though the primary modulator is the type of β-globin mutation which affects the degree of β-gl
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 35(1)
Publikováno v:
International Journal of Hematology. 99:338-344
Relationships of Swiss-type heterocellular HPFH as functions of XmnI-(G)γ and HBBP1:rs2071348 polymorphisms and HbF, HbE, MCV and MCH in HbE carriers were evaluated in 52 non-anemic and α-thalassemia-free Thai HbE carriers. HbF and HbE levels were
Autor:
Mary Ellen Hoehn, Matthew P. Smeltzer, Banu Aygun, Jeremie H. Estepp, Winfred C. Wang, Jane S. Hankins
Publikováno v:
British Journal of Haematology. 161:402-405
Elevated foetal haemoglobin (HbF) levels are protective against some manifestations of sickle cell anaemia but the impact on retinopathy is unknown. We report on 123 children with HbSS, 10.6% of whom developed retinopathy. Independent of hydroxycarba
Publikováno v:
Journal of Biotechnology. 256:S77-S78
Publikováno v:
Clinica Chimica Acta. 406:124-128
Background Patients with variant hemoglobins may receive inaccurate results by some HbA1c methods. We examined reporting practices of clinical laboratories with respect to variant hemoglobins and limitations of methodology. Methods A survey of report
Association of XmnI (-158 γG) Polymorphism and Response to Hydroxyurea in Omani S/S and S/β Patients
Publikováno v:
Journal of Genetics and Genome Research. 1
Objective: To describe the effect of Hydroxyurea (HU) treatment in Omani Sickle Cell Disease (SCD) patients with different beta-globin gene cluster haplotypes. Materials and methods: A total of 52 cases treated with HU were enrolled in this study. Re
Publikováno v:
Annals of Ibadan Postgraduate Medicine; Vol 8, No 1 (2010); 30-33
Annals of Ibadan Postgraduate Medicine
Annals of Ibadan Postgraduate Medicine
Aim: - Elevated HbF, among other biological and environmental factors, is responsible for decrease in mortality in sickle cell anaemia (SCA). This study determined the levels of HbF in adult SCA patients in steady state compared with HbAA controls. H
Autor:
Shawn Connolly, Janielle R. Bachelder, Christina M. Moellering, Steven Hanson, J D England, Curt L. Rohlfing, Randie R. Little
Publikováno v:
American journal of clinical pathology. 129(5)
Hemoglobin A 1c (HbA 1c ) is an important indicator of risk for complications in patients with diabetes mellitus. Elevated fetal hemoglobin (HbF) levels have been reported to interfere with results of some HbA 1c methods, but it has generally been as