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Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA
Taylor & Francis Verlag | 2020| -
Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition
Taylor & Francis Verlag | 2018| -
Prevalence, Incidence, Trend, and Complications of Thalassemia in Iraq
Taylor & Francis Verlag | 2017| -
Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations
Taylor & Francis Verlag | 2016| -
β-Thalassemia Major and Coronavirus-19, Mortality and Morbidity: a Systematic Review Study
Taylor & Francis Verlag | 2021| -
β-Thalassemia in Iran: Things Everyone Needs to Know About This Disease
Taylor & Francis Verlag | 2019| -
Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria
Taylor & Francis Verlag | 2019| -
The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran
Taylor & Francis Verlag | 2019| -
COVID-19 in a Patient with β-Thalassemia Major and Severe Pulmonary Arterial Hypertension
Taylor & Francis Verlag | 2020| -
Aging in Sickle Cell Disease: Co-morbidities and New Issues in Management
Taylor & Francis Verlag | 2015| -
Hematological Characteristics of β-Globin Gene Mutation –50 (G>A) (HBB: c.-100G>A) Carriers in Mainland China
Taylor & Francis Verlag | 2020| -
Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting Curve
Taylor & Francis Verlag | 2020|
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