Catherine Skari – Page 35

Aug- 2022 -

14 August

Nutritional Status in a Sample of Patients With β-Thalassemia Major

Patients suffering from thalassemia have decreased levels of lean body mass and an increased nutritional risk. The aim of this…

13 August

Scientific Literature

Safety and Efficacy of Mitapivat, an Oral Pyruvate Kinase Activator, in Adults with Non-Transfusion Dependent α-Thalassaemia or β-Thalassaemia: An Open-label, Multicentre, Phase 2 Study

Background: Patients with non-transfusion-dependent thalassaemia (NTDT), although they do not require regular blood transfusions for survival, can still accrue a heavy…

9 August

Scientific Literature

New Entity—Thalassemic Endocrine Disease: Major Beta-Thalassemia and Endocrine Involvement

Beta-thalassemia (BTH), a recessively inherited haemoglobin (Hb) disorder, causes iron overload (IO), extra-medullary haematopoiesis and bone marrow expansion with major…

3 August

Scientific Literature

2021 Thalassaemia International Federation Guidelines for the Management of Transfusion-dependent Thalassemia

Beta-thalassemia and particularly its transfusion-dependent form (TDT) is a demanding clinical condition, requiring life-long care and follow-up, ideally in specialized…

1 August

TIF Publications

A Short Guide for the Management of Transfusion-Dependent Thalassaemia (2nd edition – 2022)

Prepared by: Farmakis, D. Reviewed by: Eleſtheriou, A., Bain, B.

Jul- 2022 -

11 July

Scientific Literature

Frequency, Pattern, and Associations of Renal Iron Accumulation in Sickle/β-Thalassemia Patients

We evaluated frequency, pattern, and associations of renal iron accumulation in sickle/β-thalassemia. Thirty-three sickle/β-thalassemia patients (36.5 ± 14.7 years; 13 females), 14 homozygous…

Jun- 2022 -

18 June

News