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Published in 2021 at "Transfusion Clinique et Biologique"
DOI: 10.1016/j.tracli.2021.06.007
Abstract: Introduction: Because of iron overload complications, thrombosis and infectious predisposition, patients with severe forms of thalassemia are likely to be at increased risk of COVID-19 complications. Results: A national survey conducted during the year 2020…
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Keywords:
infection patients;
french experience;
patients thalassemia;
thalassemia french ... See more keywords
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Published in 2017 at "Hemoglobin"
DOI: 10.1080/03630269.2017.1340307
Abstract: Abstract Increased life expectancy in patients with β-thalassemia (β-thal) requires healthcare professionals to give greater attention to improving their quality of life (QoL). We aimed to evaluate health-related QoL (HRQoL) and its determinants in patients…
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Keywords:
patients thalassemia;
southern iran;
quality life;
life ... See more keywords
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Published in 2023 at "Hemoglobin"
DOI: 10.1080/03630269.2023.2208760
Abstract: Considering the importance of managing patients with β-thalassemia and the importance of early detection of disease complications, we examined the rate of sensorimotor neuropathy in patients with β-thalassemia and the risk factors related to it.…
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Keywords:
patients thalassemia;
age;
serum ferritin;
ferritin level ... See more keywords
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Published in 2019 at "Hematology"
DOI: 10.1080/10245332.2018.1540518
Abstract: ABSTRACT Objectives: This study aimed to estimate the prevalence of liver fibrosis and assess the risk factors for developing significant liver fibrosis in patients with Thalassemia Major (TM). Methods: All patients with TM over the…
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Keywords:
fibrosis;
liver fibrosis;
patients thalassemia;
fibrosis patients ... See more keywords
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Published in 2019 at "Journal of Pediatric Hematology/Oncology"
DOI: 10.1097/mph.0000000000001489
Abstract: Background: Thalassemia major is a genetic disease with a recessive autosomal pattern of inheritance that occurs as a result of disorder in hemoglobin synthesis. Researchers aimed to investigate the cutoff of ferritin for the development…
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Keywords:
cutoff;
cutoff ferritin;
thalassemia major;
hypothyroidism ... See more keywords
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Published in 2023 at "European journal of haematology"
DOI: 10.1111/ejh.13975
Abstract: BACKGROUND Patients with transfusion-dependent (TD) β-thalassemia require long-term red blood cell transfusions (RBCTs) that lead to iron overload, impacting health-related quality of life (HRQoL). METHODS The impact of luspatercept, a first-in-class erythroid maturation agent, versus…
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Keywords:
health;
patients thalassemia;
quality life;
related quality ... See more keywords
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Published in 2023 at "Acta Radiologica"
DOI: 10.1177/02841851231165283
Abstract: Background Due to the small sample size of many studies, it remained unclear what standardized reference range the T2* cutoff at 3 T would be used to assess the severity of cardiac iron load. In addition,…
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Keywords:
cardiac iron;
iron;
patients thalassemia;
quantification cardiac ... See more keywords
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Published in 2021 at "BMC Psychology"
DOI: 10.1186/s40359-021-00547-0
Abstract: Background Thalassemia have a negative impact on the patients' psychological health and sleep quality. This study aimed to determine the effects of a positive thinking training program on hope and sleep quality of patients with…
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Keywords:
quality;
trial;
patients thalassemia;
positive thinking ... See more keywords
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Published in 2019 at "PLoS ONE"
DOI: 10.1371/journal.pone.0214148
Abstract: Disease-related complications and management are different among patients with thalassemia. This study was aimed to review the prevalence, clinical risk factors for the complications and the management in patients with thalassemia in Thailand. A multicenter…
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Keywords:
related complications;
complications management;
patients thalassemia;
disease related ... See more keywords
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Published in 2022 at "Frontiers in Pharmacology"
DOI: 10.3389/fphar.2021.814302
Abstract: At present, the main therapies for ß-thalassemia patients include regular blood transfusion and iron chelation, associating with a number of limitations. Thalidomide, a fetal hemoglobin (HbF) inducer that promotes γ-globin gene expression, has been reported…
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Keywords:
efficacy safety;
response;
patients thalassemia;
meta analysis ... See more keywords
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Published in 2022 at "Diagnostics"
DOI: 10.3390/diagnostics12081920
Abstract: In patients with thalassemia major (TM), cardiac magnetic resonance feature-tracking (CMR-FT) has been shown to be an effective method for diagnosing subclinical left ventricular (LV) dysfunction. This study aimed to determine whether CMR-FT could detect…
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Keywords:
thalassemia major;
patients thalassemia;
strain;
cardiac magnetic ... See more keywords