Catherine Skari
-
Sep- 2024 -20 SeptemberNews
UNITING EXPERTS | Highlights from the 1st Nordic Red Blood Cell Meeting
The meeting, organised by the Danish Red Blood Cell Centre of the Copenhagen University Hospital – Rigshospitalet, and led by…
Read More » -
4 SeptemberNews
ANNUAL REPORT 2023 | Unveiling TIF’s Impactful Achievements
In 2023, TIF enhanced its advocacy efforts with the WHO to advance the UN Sustainable Development Goals 2030 and universal…
Read More » -
3 SeptemberNews
WORLD PATIENT SAFETY DAY 2024 | Get It Right, Make It Safe!
This year the theme is “Improving diagnosis for patient safety” with the slogan “Get it right, make it safe!”, highlighting…
Read More » -
2 SeptemberNews
REGULATORY APPROVAL | PiaSky Becomes the First Monthly Treatment for PNH in the EU
Paroxysmal Nocturnal Haemoglobinuria (PNH) is a rare and life-threatening blood condition where red blood cells are destroyed by the complement…
Read More » -
Aug- 2024 -8 AugustNews
ACCESS TO INNOVATION | UK Greenlights Gene-Editing Therapy Casgevy for β-Thalassaemia Treatment
This development opens new treatment avenues for an estimated 460 patients aged 12 and above in England who rely on…
Read More » -
Jul- 2024 -29 JulyNews
GLOBAL SURVEY | Understanding the Thalassaemia Community Health Literacy & Its Impact on Care
To improve the understanding of health literacy within the thalassemia community and how this may impact disease management and care,…
Read More » -
29 July
-
26 JulyScientific Literature
Iron Chelation Therapy for Children with Transfusion‐Dependent β‐Thalassemia: How Young Is Too Young?
In this review, we provide a summary of evidence on iron overload in young children with transfusion-dependent β-thalassemia (TDT) and…
Read More » -
25 JulyScientific Literature
Bone Health Impairment in Patients with Hemoglobinopathies: From Biological Bases to New Possible Therapeutic Strategies
Hemoglobinopathies are monogenic disorders affecting hemoglobin synthesis. Thalassemia and sickle cell disease (SCD) are considered the two major hemoglobinopathies. Thalassemia…
Read More » -
25 JulyScientific Literature
Early Detection of Renal Complication in Children With Sickle Cell Disease: A Single Center Prospective Study
Introduction: This observational cross-sectional study aimed to identify predictors of renal complications in pediatric patients with sickle cell disease (SCD)…
Read More »

