Hb S-β-Thalassemia: Molecular, Hematological and Clinical Comparisons-Reference-Cited by-同舟云学术

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Hb S-β-Thalassemia: Molecular, Hematological and Clinical Comparisons

Published:2011-01-20 Issue:1 Volume:35 Page:1-12
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Serjeant Graham R.,Serjeant Beryl E.,Fraser Raphael A.,Hambleton Ian R.,Higgs Douglas R.,Kulozik Andreas E.,Donaldson Alan

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.546306

Reference21 articles.

1. Serjeant GR, Serjeant BE. Sickle Cell Disease, 3rd ed. Oxford: Oxford University Press, 2001.

2. Estimation of Small Percentages of Fœtal Hæmoglobin

3. Microchromatographic quantitation of gemoglobin A levels in phenotypes of sickle cell-beta+ thalassemia

4. Comparison of Haematological Features of the β0and β+Thalassaemia Traits in Jamaican Negroes

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1. The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β‐thalassaemia and no or low HbA expression;European Journal of Haematology;2024-06-30

2. Clinical, laboratory, and molecular characteristics of a cohort of children with hemoglobinopathy S/beta-thalassemia;Hematology, Transfusion and Cell Therapy;2023-12

3. Doping control approach: Identification of equine in vitro metabolites of voxelotor (GBT440), a hemoglobin S polymerization inhibitor;Rapid Communications in Mass Spectrometry;2023-11-28

4. Stratification of βSβ+ Compound Heterozygotes Based on L-Glutamine Administration and RDW: Focusing on Disease Severity;Antioxidants;2023-11-08

5. Management of gingival hyperpigmentation induced by increased ferritin level in a HbS‐β⁺ thalassemia patient using diode laser;Clinical Case Reports;2023-11

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