Hemoglobin sickle cell disease complications: a clinical study of 179 cases-Reference-Cited by-同舟云学术

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Hemoglobin sickle cell disease complications: a clinical study of 179 cases

Published:2012-02-07 Issue:8 Volume:97 Page:1136-1141
ISSN:0390-6078
Container-title:Haematologica
language:en
Short-container-title:Haematologica

Author:

Lionnet F.,Hammoudi N.,Stojanovic K. S.,Avellino V.,Grateau G.,Girot R.,Haymann J.-P.

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Cited by 116 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. Automated red blood cell exchange with a post‐procedure haematocrit targeted at 34% in the chronic management of sickle cell disease;British Journal of Haematology;2024-07-30

2. 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

3. Constitutive hypercoagulability in pediatric sickle cell disease patients with hemoglobin SS genotype;Research and Practice in Thrombosis and Haemostasis;2024-03

4. Drepanocitosis y dolor en niños: descripción y tratamiento analgésico de los episodios vasooclusivos;EMC - Pediatría;2024-03

5. Iron restriction in sickle cell disease: When less is more;American Journal of Hematology;2024-02-23

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