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

Blood transfusion therapy for β‐thalassemia major and hemoglobin E β‐thalassemia: Adequacy, trends, and determinants in Sri Lanka

(2019) Sachith Mettananda et al.   PEDIATRIC BLOOD & CANCER

A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?

(2018) Maria Domenica Cappellini et al.   BLOOD REVIEWS

Health-related quality of life in pediatric and adolescent patients with transfusion-dependent ß-thalassemia in upper Egypt (single center study)

(2018) Gehan L Abdel Hakeem et al.   Health and Quality of Life Outcomes

Molecular Basis and Genetic Modifiers of Thalassemia

(2018) Sachith Mettananda et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Clinical Complications and Their Management

(2018) Alessia Marcon et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Non-Transfusion-Dependent Thalassemia: An Update on Complications and Management

(2018) Joseph Sleiman et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Thalassaemia

(2018) Ali T Taher et al.   LANCET

Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia

(2018) Alexis A. Thompson et al.   NEW ENGLAND JOURNAL OF MEDICINE

How I manage medical complications of beta-thalassemia in adults

(2018) Ali T. Taher et al.   BLOOD

Health-related quality of life (HRQoL) in beta-thalassemia major (β-TM) patients assessed by 36-item short form health survey (SF-36): a meta-analysis

(2018) Mahdieh Arian et al.   QUALITY OF LIFE RESEARCH

Anaemia among females in child-bearing age: Relative contributions, effects and interactions of α- and β-thalassaemia

(2018) Sachith Mettananda et al.   PLoS One

Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia

(2017) Sachith Mettananda et al.   Nature Communications

Psychological maladjustment and quality of life in adolescents with constipation

(2016) Nishadi Ranasinghe et al.   ARCHIVES OF DISEASE IN CHILDHOOD

The evolutionary and clinical implications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances

(2016) Anuja Premawardhena et al.   BRITISH JOURNAL OF HAEMATOLOGY

Selective silencing of α-globin by the histone demethylase inhibitor IOX1: a potentially new pathway for treatment of β-thalassemia

(2016) Sachith Mettananda et al.   HAEMATOLOGICA

Selective silencing of α-globin by the histone demethylase inhibitor IOX1: a potentially new pathway for treatment of β-thalassemia

(2016) Sachith Mettananda et al.   HAEMATOLOGICA

 -Globin as a molecular target in the treatment of  -thalassemia

(2015) S. Mettananda et al.   BLOOD

BCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesis

(2015) Matthew C. Canver et al.   NATURE

Quality of life and health care consultation in 13 to 18 year olds with abdominal pain predominant functional gastrointestinal diseases

(2014) Niranga Manjuri Devanarayana et al.   BMC GASTROENTEROLOGY

Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia major

(2013) Robert J. Klaassen et al.   BRITISH JOURNAL OF HAEMATOLOGY

Psychometric properties of the Sinhala version of the PedsQL™ 4.0 Generic Core Scales in early adolescents in Sri Lanka

(2012) Manjula Danansuriya et al.   Health and Quality of Life Outcomes

The challenge of haemoglobinopathies in resource-poor countries

(2011) David J. Weatherall   BRITISH JOURNAL OF HAEMATOLOGY

Thalassaemia

(2011) Douglas R Higgs et al.   LANCET

Studies in haemoglobin E beta-thalassaemia

(2010) Nancy F. Olivieri et al.   BRITISH JOURNAL OF HAEMATOLOGY