Results 41 to 50 of about 72,054 (299)

STUDY OF FETAL HEMOGLOBIN WITH GESTATIONAL AGE, BIRTH WEIGHT AND RETINOPATHY OF PREMATURITY IN PRETERM INFANTS

open access: yesIJRETINA (International Journal of Retina), 2023
Introduction: The objective of this study was to find an association of fetal hemoglobin (HbF) with gestational age, birth weight and retinopathy of prematurity (ROP) in preterm infants. Methods: Observational prospective study. We included a total of
Nishi Prasad   +3 more
doaj   +1 more source

Hemoglobin: A Biochemical and Molecular Overview [PDF]

open access: yes, 2020
This book brings together a selection of chapters dedicated to fetal hemoglobin - its physiological role, regulation, methodologies to manipulate and future strategies.No Full ...
Rahman, Motiur   +4 more
core  

Cell free hemoglobin in the fetoplacental circulation: a novel cause of fetal growth restriction? [PDF]

open access: yes, 2018
Cell free hemoglobin impairs vascular function and blood flow in adult cardiovascular disease. In this study, we investigated the hypothesis that free fetal hemoglobin (fHbF) compromises vascular integrity and function in the fetoplacental circulation ...
Greenwood, Susan L   +14 more
core   +1 more source

Association of HMIP1 C-893A polymorphism and disease severity in patients with sickle cell anemia

open access: yesHematology, Transfusion and Cell Therapy, 2021
Introduction: Sickle cell anemia (SCA) is a Mendelian disorder with a heterogeneous clinical course. The reasons for this phenotypic diversity are not entirely established, but it is known that high fetal hemoglobin levels lead to a milder course of the ...
Diego A. Pereira-Martins   +9 more
doaj   +1 more source

Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse model

open access: yesHaematologica, 2010
Hydroxyurea has proven clinical efficacy in patients with sickle cell disease. Potential mechanisms for the beneficial effects include fetal hemoglobin induction and the reduction of cell adhesive properties, inflammation and hypercoagulability.
Jeffrey D. Lebensburger   +4 more
doaj   +1 more source

Metabolic persistence of fetal hemoglobin [PDF]

open access: yesBlood, 1995
Hereditary persistence of fetal hemoglobin (HPFH) has typically been ascribed to mutations in the beta-globin gene cluster. Pharmacologic agents, including the short-chain fatty acid butyrate, have been shown to upregulate fetal and embryonic globin gene expression. In this report we investigate the possibility that metabolic derangements characterized
J A, Little   +3 more
openaire   +2 more sources

Agreement between HbA1c measured by DCA 2000 and by HPLC: effects of fetal hemoglobin concentrations [PDF]

open access: yes, 2004
In subjects with type 1 diabetes, persisting elevations of fetal hemoglobin (HbF) have been demonstrated. This study evaluated whether HbF levels typically seen in type 1 diabetes (up to 3%) interfere with glycohemoglobin determinations using a common ...
Wälchli, M   +3 more
core   +1 more source

What influences Hb fetal production in adulthood?

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2011
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respectively. Different types of hemoglobin are synthesized according to the stage of development with fetal hemoglobin (α2γ2) (Hb F) being ...
Gisele Cristine de Souza Carrocini   +2 more
doaj   +1 more source

Oxidative stress in preeclampsia and the role of free fetal hemoglobin

open access: yesFrontiers in Physiology, 2015
Preeclampsia is a leading cause of pregnancy complications and affects 3–7 % of pregnant women. This review summarizes the current knowledge of a new potential etiology of the disease, with a special focus on hemoglobin-induced oxidative stress ...
Stefan Rocco Hansson   +2 more
doaj   +1 more source

Haematological Characterisation and Molecular Basis of Asian Indian Inversion Deletions Delta Beta Thalassemia: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
The hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia are heterogeneous disorders characterised by increased levels of fetal hemoglobin and high level of this Hb continues in adulthood.
Jitender Mohan Khunger   +4 more
doaj   +1 more source

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