Co-inheritance of a-thalassemia dramatically decreases the risk of acute splenic sequestration in a large cohort of newborns with hemoglobin SC-Reference-Cited by-同舟云学术

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Co-inheritance of a-thalassemia dramatically decreases the risk of acute splenic sequestration in a large cohort of newborns with hemoglobin SC

Published:2019-01-10 Issue:7 Volume:104 Page:e281-e283
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Rezende Paulo V.,Belisário André R.,Oliveira Érica L.,Almeida Jéssica A.,Oliveira Larissa M. M.,Muniz Maristela B.S.R.,Viana Marcos B.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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

2. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

3. Determinants of severity in sickle cell disease;Blood Reviews;2022-11

4. 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 not translate into increased survival;American Journal of Hematology;2022-07-18

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