Iranian Journal of Psychiatry, 2018 Objective: Thalassemia is one of the most frequent monogenic disorders, leading to impairment in the maturation and survival of red blood cells. The question examined here is whether, and if so, to what extent, people with beta-thalassemia might also be ...
Mohammad Ahmadpanah +5 more
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HUBUNGAN ANTARA STRES DENGAN STRATEGI COPING PADA ORANG TUA YANG MEMILIKI ANAK PENDERITA TALASEMIA BETA MAYOR DI RUMAH SAKIT UMUM DAERAH DR. ZAINOEL ABIDIN BANDA ACEH [PDF]
, 2013 Background: Beta thalassemia major is a disorder characterized by defective hemoglobin production and excessive destruction of red blood cells. This life-threatening illnesses suffered by children can lead to parental stress and depression. How to cope
RINA SYAFRITA
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Gallstones and Choledocolithiasis with Severe Cholestatic Jaundice in Beta-Thalasemia Intermedia Patient [PDF]
, 2014 Geographically, b-thalassemia can be found in many countries including in Indonesia. Thalassemia intermedia referred to patients as being ‘too haematologically severe to be called minor, but too mild to be called major\u27.
Bayupurnama, P. (Putut) +3 more
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Fuzzy-Based Fusion Model for β-Thalassemia Carriers Prediction Using Machine Learning Technique
Advances in Fuzzy SystemsThe abnormality of haemoglobin in the human body is the fundamental cause of thalassemia disease. Thalassemia is considered a common genetic blood condition that has received extensive investigation in medical research globally.
Muhammad Ibrahim +9 more
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Oxidative stress and antioxidant status in beta-thalassemia heterozygotes
Revista Brasileira de Hematologia e Hemoterapia, 2013 Background: Several studies have evaluated the oxidant and antioxidant status of thalassemia patients but most focused mainly on the severe and intermediate states of the disease.
Luciana de Souza Ondei +6 more
doaj +1 more source
Quality of life among patients with beta-thalassemia major in Shahrekord city, Iran [PDF]
, 2016 Background and aims: Nowadays introduction of regular blood transfusion therapy has obviously improved the life expectancy of patients with thalassemia. However, these patients face with newer challenges which influence their quality of life (QoL).
Emadi Dehaghi, B. +2 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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Approaches to Management of Beta-Thalassemia Intermedia
Thalassemia Reports, 2013 Thalassemia intermedia is a genetically diverse group of diseases that is the result of an imbalance in the production of the alpha and beta chains with ensuing chronic hemolysis, ineffective erythropoiesis, and iron overload.Resulting complications include bone changes, hypercoagulability, and end-organ damage due to iron overload.
Maakaron, Joseph E., Taher, Ali T.
openaire +4 more sources
The Application of Clinical Genetics, 2014 Boonchai Boonyawat,1 Chalinee Monsereenusorn,2 Chanchai Traivaree2 1Division of Genetics, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand; 2Division of Hematology/Oncology, Department of Pediatrics ...
Boonyawat B +2 more
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Prevalence and intensity of depression in mothers of children with beta-thalassemia major in Talghani Hospital of Gorgan, Iran [PDF]
, 2014 Background: Thalassemia is a chronic disease that it leads to psychological and social problems for parents. Mothers are at markedly increased risk of suffering from psychological distress and depression because they usually take on a considerable part ...
Jahazi, A. +3 more
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