Results 71 to 80 of about 39,321 (195)
Journal of Pure and Applied Microbiology, 2018 Thalassemia is a genetic disorder occurs as a result of the imbalance in the construction of haemoglobin chains cause haemolytic anaemia. This study was aimed to evaluate the serum level of immunological parameters (Transforming growth factor beta1 ...
Rusul Malik Al-Dedah +4 more
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Pulmonary hypertension in adolescents with sickle cell disease [PDF]
, 2016 Sickle cell disease consists of a group of disorders that have a similar mutation in at least one of the beta-globin chains of hemoglobin. This results in a change of the hemoglobin to sickle shaped cells when in the deoxygenated state.
Akinyemi, Katherine
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Survival Probability in Patients with Sickle Cell Anemia Using the Competitive Risk Statistical Model. [PDF]
, 2019 The clinical picture of patients with sickle cell anemia (SCA) is associated with several complications some of which could be fatal. The objective of this study is to analyze the causes of death and the effect of sex and age on survival of Brazilian ...
Ballas, Samir K. +3 more
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A validated cellular biobank for β-thalassemia [PDF]
, 2016 Background: Cellular biobanking is a key resource for collaborative networks planning to use same cells in studies aimed at solving a variety of biological and biomedical issues. This approach is of great importance in studies on β-thalassemia, since the
BIANCHI, Nicoletta +15 more
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Comparative frequency of Coagulation Factor II and Coagulation Factor V Alleles among new-born and senior citizens [PDF]
, 2005 Resistance to activated protein C is one of the most common inherited disorders associated with hereditary thrombophilia. A missense mutation in the gene coding for coagulation factor V (CF V Leiden) and which renders this procoagulant factor resistant ...
Abela Medici, Joseph +4 more
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Epistasis and the sensitivity of phenotypic screens for beta thalassaemia [PDF]
, 2014 Genetic disorders of haemoglobin, particularly the sickle cell diseases and the alpha and beta thalassaemias, are the commonest inherited disorders worldwide.
Gupta, Sunetra +2 more
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Does vitamin E have a role in treatment and prevention of anemia? [PDF]
, 2011 Vitamin E is a highly effective fat-soluble vitamin with a variety of cellular membrane stabilizing-antioxidant and non-antioxidant functions. Vitamin E has been suggested to prevent the oxidation of polyunsaturated fatty acids in red blood cell (RBC ...
Iqbal, Mohammad Perwaiz, Jilani, Tanveer
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Long-term treatment with deferiprone enhances left ventricular ejection function when compared to deferoxamine in patients with thalassemia major [PDF]
, 2013 Transfusion and iron chelation treatment have significantly reduced morbidity and improved survival of patients with thalassemia major. However, cardiac disease continues to be the most common cause of death.
Barone, R +18 more
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Research in Molecular Medicine, 2017 Alpha Thalassemia is one of the most prevalent disorders worldwide with a [T1] high carrier rate in Mazandaran province (north of Iran). Carriers of --MED double gene deletion are at risk of having a child with hemoglobin haemoglobin[T2]
Hossein Jalali +3 more
doaj
Effect of sex class on the levels of some biochemical variables in thalassemia patients
Tikrit Journal of Pure Science, 2019 The study was conducted at Azadi Teaching Hospital - Thalassemia Center for the period from 1/10/2017 to 1/4/2018. It included 60 patients including 30 males and 30 females, as well as control group which included 20 Healthy people were all 10 to 21 ...
Khalaf N. Mohammed, Mossa M. Marbut
doaj +1 more source