Zobrazeno 1 - 8
of 8
pro vyhledávání: '"beta-Thalassemia blood"'
Publikováno v:
Diyala Journal of Medicine, Vol 13, Iss 1 (2018)
Background: Thalassemia is one of the most common genetic diseases in the world. It is a major health problem, causing much morbidity. The prevalence of hepatitis C virus (HCV) among multi-transfused patients varies from one area to another and depen
Externí odkaz:
https://doaj.org/article/5add131106484622bcfe4114e00e207c
Publikováno v:
Bali Medical Journal, Vol 8, Iss 2, Pp 592-595 (2019)
Background: The prognosis of patients with beta-thalassemia major has improved in the last few decades, but some complications occur in thalassemia patients such as the prolongation of blood coagulation time. This study aimed to determine the differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::957f30613b766f1de7baa1a4785995c2
https://doi.org/10.15562/bmj.v8i2.1412
https://doi.org/10.15562/bmj.v8i2.1412
Autor:
Nikolaos Chaliasos, Eleftheria Hatzimichael, Dimitrios K. Bourantas, Freideriki Koutsouka, Anna Challa, Konstantinos L. Bourantas, Alexandros Makis, Antigone Siamopoulou, Antonios P. Vlahos
Publikováno v:
Acta Haematologica. 124:191-196
Background/Aim: The adipocytokines leptin and adiponectin represent a critical link between metabolism, immunity and chronic inflammation. A chronic vascular inflammatory state plays an important role in the pathophysiology of thalassaemia. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9bebdda25e744c6ca51fe4a0e781706
https://doi.org/10.1159/000320274
https://doi.org/10.1159/000320274
Thalassemia major (TM) results in hemolytic anemia, an increase in intestinal iron absorption, and occurrence of iron loading due to erythrocyte transfusion; the disease is characterized by oxidative damage in major organs. Oxidative stress leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::e84d76b4b469583bb75764ae5402b6a5
Background. Beta-thalassemia is an inherited blood disorder. It results from the impaired production of ß-globin chains, leading to a relative excess of alpha-globin chains. Clinical severity separates this disease into three main subtypes: ß- thal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5574aa371e86c17c82cc8a9c7dc0771d
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/7543
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/7543
In this study we first aimed to investigate the value of soluble transferrin receptor levels (sTfR) in healthy, iron deficient and beta thalassemia trait children and to determine whether sTfR is a useful indicator of iron deficiency. Secondly, we in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::fca280a60a4f80017fbf77185f127751
Serum levels of the vitamin D metabolites 25-hydroxyvitamin D, 24,25-dihydroxyvitamin D, and 1,25-dihydroxyvitamin D, and of osteocalcin, C-terminal parathyroid hormone and other biochemical indices related to bone metabolism, were determined in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::e498f26f500e0558e5ece7046a2aee77
http://olympias.lib.uoi.gr/jspui/handle/123456789/24505
http://olympias.lib.uoi.gr/jspui/handle/123456789/24505