Asian Journal of Medical SciencesBackground: Hemoglobinopathies are the most commonly inherited red cell disorder around the world. In India, hemoglobinopathies show wide variation of prevalence in different regions and different populations.
Arnab Sinha +2 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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Erythrocytapheresis as a novel treatment option for adult patients with pyruvate kinase deficiency
Haematologica, 2020 Rawia F.G. Jensen +4 more
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Microalbuminuria as Predictor of Early Glomerular Injury in Children and Adolescents with Sickle Cell Anaemia at Muhimbili National Hospital Dar es Salaam, Tanzania 2012 [PDF]
, 2012 Microalbuminuria (MA) is the earliest marker of various diseases affecting the renal system. Its relevance in children and adolescents with sickle cell anaemia (SCA), who are known to be prone to renal complications, has not been fully explored in our ...
Christopher, Richard
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Reticulocyte parameters in hemoglobinopathies and iron deficiency anemia [PDF]
, 2003 Laura C. Cortellazzi +5 more
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, 2017 This article answers the question: My patient carries a diagnosis of chronic anemia and has been treated for irondeficiency in the past with minimal to no improvement.
Coberly, Emily, Ringling, Rebecca
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A New Hereditary Hemoglobinopathy (the Lepore Trait) and Its Interaction with Thalassemia Trait [PDF]
, 1958 Park S. Gerald, Louis K. Diamond
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Hemoglobinopathy pattern among school and college students in Marathwada region of Maharashtra: A study of 500 students [PDF]
, 2020 Subhas G Kabade, Bharat R Sonwane
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Comparative efficacy of deferiprone, deferoxamine and combination of deferiprone and deferoxamine on serum ferritin value in Beta-Thalassemia patients [PDF]
, 2015 Background: Iron overload is a predictable and life-threatening complication in patients with thalassemia. Effective and convenient iron chelation remains one of the main targets of clinical management of thalassemia major.
Amlashi, H.M. +3 more
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