Catherine Skari
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Apr- 2023 -10 AprilNews
NEW PUBLICATION | Guidelines for the Management of Non-Transfusion-Dependent β-Thalassaemia
This novel edition is an invaluable contribution in upgrading the care of individuals with NTDT, a condition that has been…
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8 April
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2 AprilNews
G6PD | Common Enzyme Deficiency Linked with COVID Severity
In Black men under 65, for example, those with the common enzyme deficiency had a roughly 1.5-fold higher risk for…
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Mar- 2023 -28 MarchNews
TIF’s Executive Director Chosen Among ‘Women Who Advance Associations 2023′
‘Women Who Advance Associations’ celebrates the great talent of the international association community. For International Women’s Day, marked annually on…
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26 MarchNews
INTERNATIONAL THALASSAEMIA DAY 2023 | The Official Page Is Now Live!
Head to the official webpage https://thalassaemia.org.cy/itd2023/ to explore the fantastic International Thalassaemia Day resources and activities, learn more about…
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24 MarchScientific Literature
Deferiprone for Transfusional Iron Overload in Sickle Cell Disease and Other Anemias: Open-label Study of Up to 3 Years
Long-term safety and efficacy data on the iron chelator deferiprone in sickle cell disease (SCD) and other anemias are limited.…
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20 MarchScientific News
Expecting More: The Case for Incorporating Fertility Services into Comprehensive Sickle Cell Disease Care
In recent years, advances in the medical care of sickle cell disease including optimal blood transfusion, the use of hydroxyurea…
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18 MarchScientific News
A Novel, Effective, and Efficient Strategy for Treating Sickle Cell Vaso-occlusive Events in the Infusion Center Setting
Coagulation factors are proteins in our blood, and they help form blood clots to stop bleeding when is needed. There…
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16 MarchScientific News
Splenectomy in Sickle Cell Disease: Do Benefits Outweigh Risks?
Spleen is an organ in the abdomen that plays an important role in immune system being a key-role organ in…
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15 MarchNews
NEW REVIEW | Treatment Landscape of Rare Anaemias Is Shifting Rapidly
Writing in Frontiers in Medicine, the authors began by reviewing congenital and acquired forms of anaemia. Those include sickle cell disease…
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