Where I see patients (2)
Selected research
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Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial.
Lancet (London, England)
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Hemoglobin Balkh, a Novel Mutation in Codon 132 of α2-Globin Gene [α132(H15) (+T) or HBA2:C.396dup (p.Val134fs)]: A Case Report and Insight into the Pathophysiology.
Hemoglobin
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Disease burden, management strategies, and unmet needs in α-thalassemia due to hemoglobin H disease.
American journal of hematology
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Tender wagging care
Our therapy dogs spread joy and smiles at the bedside and throughout the hospital.
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