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The pleiotropic effects of α‐thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co‐transport activity, serum erythropoietin, and transfusion burden, do no...
by
Brewin, John N.
,
Nardo‐Marino, Amina
,
Stuart‐Smith, Sara
,
El Hoss, Sara
,
Hanneman, Anke
,
Strouboulis, John
,
Menzel, Stephan
,
Gibson, John S.
,
Rees, David C.
Published in
American journal of hematology
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American Journal Of Hematology
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Alpha-Thalassemia - Complications
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Alpha-Thalassemia - Therapy
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Anemia, Sickle Cell - Complications
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Blood Diseases
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Cations
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Erythrocytes
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Erythropoietin
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Hematology
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Hemoglobin
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Hemoglobin Sc Disease
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Hemoglobin, Sickle - Genetics
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Humans
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Life Sciences & Biomedicine
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Oxygenation
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Patients
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Phenotypes
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Potassium
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Potassium Chloride
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Proteinuria
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