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Management of Thalassaemia

Sri Lanka journal of child health, 2018-06, Vol.47 (2), p.159

Mettananda, Sachith

2018

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Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study

Health and quality of life outcomes, 2019-08, Vol.17 (1), p.137-137, Article 137

2019

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Characterization of Iron Complexes in the Red Blood Cells of β-thalassaemia patients using 57Fe Mössbauer Spectroscopy

Journal of molecular structure, 2021-04, Vol.1229, p.129732, Article 129732

2021

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When to consider transfusion therapy for patients with non-transfusion-dependent thalassaemia

Vox sanguinis, 2015-01, Vol.108 (1), p.1-10

2015

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The Danish national haemoglobinopathy screening programme: Report from 16 years of screening in a low-prevalence, non-endemic region

British journal of haematology, 2024-01, Vol.204 (1), p.329-336

2024

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Cell erythroid maturation approach: a new paradigm in the road map towards a cure for β‐thalassaemia syndromes

British journal of haematology, 2022-02, Vol.196 (4), p.806-808

Maggio, Aurelio

2022

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Novel therapies in β‐thalassaemia

British journal of clinical pharmacology, 2022-06, Vol.88 (6), p.2509-2524

2022

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Long‐term sequential deferiprone and deferasirox therapy in transfusion‐dependent thalassaemia patients: a prospective clinical trial

British journal of haematology, 2019-09, Vol.186 (6), p.e209-e211

2019

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Management of iron deficiency anaemia in children

Sri Lanka journal of child health, 2023-06, Vol.52 (2), p.204-208

Mettananda, Sachith

2023

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Hydroxyurea reduces the blood transfusion burden in patients with thalassaemia

Sri Lanka journal of child health, 2022-12, Vol.51 (4), p.647

Mettananda, Sachith

2022

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Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis

British journal of haematology, 2020-12, Vol.191 (5), p.897-905

2020

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Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

British journal of clinical pharmacology, 2022-08, Vol.88 (8), p.3610-3626

2022

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GDF15 molecule is responsible for low body mass index in children with thalassaemia

Sri Lanka journal of child health, 2024-03, Vol.53 (1), p.88

Mettananda, Sachith

2024

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When a synonymous mutation breaks the silence in a thalassaemia patient

British journal of haematology, 2024-02, Vol.204 (2), p.677-682

2024

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Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia

British journal of haematology, 2022-06, Vol.197 (5), p.609-617

2022

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Dominant β-thalassaemia with unusually high Hb A 2 and Hb F caused by β CD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene

Journal of clinical pathology, 2020-08, Vol.73 (8), p.511-513

2020

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The effect of erythroferrone suppression by transfusion on the erythropoietin–erythroferrone–hepcidin axis in transfusion‐dependent thalassaemia: A pre–post cohort study

British journal of haematology, 2023-05, Vol.201 (3), p.547-551

2023

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Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review

Annals of medicine (Helsinki), 2022-12, Vol.54 (1), p.764-774

2022

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Markers of ineffective erythropoiesis in non-transfusion dependent β-thalassaemia

Medical journal of Malaysia, 2021-01, Vol.76 (1), p.41-45

2021

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Delta globin gene variations leading to reduction in HbA2 levels

International journal of laboratory hematology, 2016-12, Vol.38 (6), p.610-615

2016

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Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia

British journal of haematology, 2000-11, Vol.111 (2), p.467-473

2000

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MicroRNA‐2355‐5p regulates γ‐globin expression in human erythroid cells by inhibiting KLF6

British journal of haematology, 2021-04, Vol.193 (2), p.401-405

2021

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Hearing loss in beta‐thalassaemia: An Italian multicentre case–control study

British journal of haematology, 2024-05, Vol.204 (5), p.2016-2024

2024

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Management of luspatercept therapy in patients with transfusion‐dependent β‐thalassaemia

British journal of haematology, 2023-06, Vol.201 (5), p.824-831

2023

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Myocardial tissue characterization by segmental T2 mapping in thalassaemia major: detecting inflammation beyond iron

European heart journal cardiovascular imaging, 2023-09, Vol.24 (9), p.1222-1230

2023

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Management of Thalassaemia

Health related quality of life among children with transfusion dependent β-thalassaemia major and haemoglobin E β-thalassaemia in Sri Lanka: a case control study

Characterization of Iron Complexes in the Red Blood Cells of β-thalassaemia patients using 57Fe Mössbauer Spectroscopy

When to consider transfusion therapy for patients with non-transfusion-dependent thalassaemia

The Danish national haemoglobinopathy screening programme: Report from 16 years of screening in a low-prevalence, non-endemic region

Cell erythroid maturation approach: a new paradigm in the road map towards a cure for β‐thalassaemia syndromes

Novel therapies in β‐thalassaemia

Long‐term sequential deferiprone and deferasirox therapy in transfusion‐dependent thalassaemia patients: a prospective clinical trial

Management of iron deficiency anaemia in children

Hydroxyurea reduces the blood transfusion burden in patients with thalassaemia

Co‐morbidities and mortality associated with transfusion‐dependent beta‐thalassaemia in patients in England: a 10‐year retrospective cohort analysis

Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

GDF15 molecule is responsible for low body mass index in children with thalassaemia

When a synonymous mutation breaks the silence in a thalassaemia patient

Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia

Dominant β-thalassaemia with unusually high Hb A 2 and Hb F caused by β CD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene

The effect of erythroferrone suppression by transfusion on the erythropoietin–erythroferrone–hepcidin axis in transfusion‐dependent thalassaemia: A pre–post cohort study

Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review

Markers of ineffective erythropoiesis in non-transfusion dependent β-thalassaemia

Delta globin gene variations leading to reduction in HbA2 levels

Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia

MicroRNA‐2355‐5p regulates γ‐globin expression in human erythroid cells by inhibiting KLF6

Hearing loss in beta‐thalassaemia: An Italian multicentre case–control study

Management of luspatercept therapy in patients with transfusion‐dependent β‐thalassaemia

Myocardial tissue characterization by segmental T2 mapping in thalassaemia major: detecting inflammation beyond iron

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