Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Foetal haemoglobin"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 05, Pp 14-17 (2024)
Compound heterozygous Sickle Haemoglobin (HbS) beta (β) thalassaemia arises from the mutations associated with sickle cell and β thalassaemia and significantly affects populations in low income countries like India. Elevated levels of Haemoglobin A
Externí odkaz:
https://doaj.org/article/4cfb4b69016f4e40abcd5fd0a11e4923
Autor:
Ama Gyasiwaah Owusu-Poku, Daniel Gyamfi, Eliezer Togbe, Stephen Opoku, Richard Kobina Dadzie Ephraim, Jocelyn Gyapomaa Asibey, Benedict Sackey, Wina Ivy Ofori Boadu, Max Efui Annani-Akollor, Enoch Odame Anto, Otchere Addai-Mensah
Publikováno v:
Human Nutrition & Metabolism, Vol 30, Iss , Pp 200173- (2022)
Foetal haemoglobin (HbF) has been speculated to have an impact on the quantity of micronutrients and the latter also have a role to play in oxidative stress (OS) in sickle cell anaemia (SCA). No previous study in Ghana has examined the interplay of t
Externí odkaz:
https://doaj.org/article/f068d2e19ddf451793ee804e58eae1b4
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 16, Iss 8, Pp EC17-EC20 (2022)
Introduction: Childhood anaemia may be caused due to many factors, including malnutrition, chronic infections, deficiency of iron and vitamins, parasitic infections. On haematological work up the most common finding is microcytic hypochromic anaemia.
Externí odkaz:
https://doaj.org/article/4ad6a170e63749239fa7977d06734b2c
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 09, Iss 02, Pp 88-93 (2020)
Delta-beta Thalassemia is a rare variant of thalassemia with elevated Hb F. Heterozygous and homozygous state of delta-beta thalassemia present with features similar to Hereditary Persistence of Fetal Haemoglobin (HPFH) and beta thalassemia inter
Externí odkaz:
https://doaj.org/article/949610a7e5664c2d8b1523a2195b6e8e
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Introduction Patients with a homozygous β0‐thalassemia mutation usually have a transfusion‐dependent β‐thalassemia major phenotype. However, some β‐thalassemia patients present with a relatively mild and even normal phenotype and
Externí odkaz:
https://doaj.org/article/ffd9f6e8819d4489b6bd22d18de0988a
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 7229 (2021)
β-thalassaemia is a rare genetic condition caused by mutations in the β-globin gene that result in severe iron-loading anaemia, maintained by a detrimental state of ineffective erythropoiesis (IE). The role of multiple mechanisms involved in the pa
Externí odkaz:
https://doaj.org/article/9aae6efd9a1e43b59730648b5a28d8bb
Autor:
Morenike Agnes Akinlosotu, Samuel Ademola Adegoke, Saheed Babajide Oseni, Oluwagbemiga Oyewole Adeodu
Publikováno v:
Nigerian Postgraduate Medical Journal, Vol 24, Iss 4, Pp 195-200 (2017)
Background: Foetal haemoglobin (HbF, α2γ2) retards polymerisation of haemoglobin (Hb) in sickle cell anaemia (SCA). In Nigeria, studies on the levels of HbF and its relationship with haematological indices are scanty. This study evaluated HbF conce
Externí odkaz:
https://doaj.org/article/8e9ecf2cf1574def98d4358c04ced65a
Autor:
Mariana Delgadinho, Catarina Ginete, Brígida Santos, Joana Mendes, Armandina Miranda, Jocelyne Vasconcelos, Miguel Brito
Sickle cell disease (SCD) is one of the most common genetic conditions worldwide. It can contribute up to 90% of under-5 mortality in sub-Saharan Africa. Clinical manifestations are very heterogeneous, and the intestinal microbiome appears to be cruc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ae9d6072248df7bd16c8b92307bacc
https://hdl.handle.net/10400.18/8516
https://hdl.handle.net/10400.18/8516
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017063-e2017063 (2017)
Background: Foetal haemoglobin (HbF) is a major modifying factor influencing sickle cell disease (SCD) severity. Despite this, HbF estimation is not routinely done in Nigeria. Relationship between HbF and SCD severity among affected children is also
Externí odkaz:
https://doaj.org/article/a5c4524daffb436ead3e09b81204860a