Catherine Skari

l-glutamine, crizanlizumab, voxelotor, and cell-based therapy for adult sickle cell disease: Hype or hope?

For more than two decades, hydroxyurea was the only therapeutic agent approved by the Food and Drug Administration (FDA) for sickle cell disease (SCD).…

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Kidney Stones in Transfusion-Dependent Thalassemia: Prevalence and Risk Factors

As patients with transfusion-dependent thalassemia (TDT) are living longer, novel morbidities are being recognized. The purpose of this review is…

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Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries

The Global Globin Network (GGN) is a project-wide initiative of the Human Variome/Global Variome Project (HVP) focusing on haemoglobinopathies to…

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Pregnancy Outcomes Among Women Affected with Thalassemia Traits

Objective To compare the maternal and perinatal outcomes between a group of pregnant women diagnosed with thalassemia traits and normal…

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Early Detection of Iron Overload Cardiomyopathy in Transfusion Dependent Thalassemia Patients in Sulaimaniyah City, Iraq

Lifelong blood transfusion is recommended for patients with transfusion-dependent thalassemia (TDT) that lead to iron overload and results in cardiomyopathy…

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NEW WHO REPORT | Effective TB, HIV, Viral Hepatitis Services For Refugees And Migrants Across The WHO European Region

International recommendations on effective services to treat tuberculosis (TB), HIV and viral hepatitis for refugees and migrants lack implementation across…

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Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell Disease

BACKGROUND Sickle cell disease is characterized by the painful recurrence of vaso-occlusive events. Gene therapy with the use of LentiGlobin…

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Iron Overload Status in Patients with Non-Transfusion-Dependent Thalassemia in China

Background: Non-transfusion-dependent thalassemia (NTDT) is a genetic disorder most commonly including beta-thalassemia intermedia (Beta-TI), HbE/Beta thalassemia (HbE/Beta thalassemia), and hemoglobin H…

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Nutrition in Thalassemia: A Systematic Review of Deficiency, Relations to Morbidity, and Supplementation Recommendations

Reports of nutritional deficiencies in patients with thalassemia (Thal) are common. Despite its importance, however, nutritionally focused research in Thal…

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Morbidity-free Survival and Hemoglobin Level in Non-Transfusion-Dependent β-Thalassemia: A 10-Year Cohort Study

No abstract available.

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