Acute splenic complications in children with sickle cell–hemoglobin C disease
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference28 articles.
1. The spleen;Serjeant,1985
2. Determinants of hemoglobin level in sickle cell-hemoglobin C disease;Bannerman;Br J Haematol,1973
3. The clinical features of sickle-cell/beta thalassemia in Jamaica;Serjeant;Br J Haematol,1973
4. Clinical triad of massive splenic infarction associated with high-altitude flying;Cooley;JAMA,1954
5. Splenic infarction following air travel and associated with the sickling phenomenon;Doenges;JAMA,1954
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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. The clinical spectrum of HbSC sickle cell disease‐not a benign condition;British Journal of Haematology;2024-06-19
3. Pediatric splenic infarction: Assessment of associated clinical conditions and outcome;Pediatric Blood & Cancer;2024-03-10
4. The Spleen and Sickle Cell Anemia;The Spleen;2023
5. Splenectomy in sickle cell disease: do benefits outweigh risks?;Haematologica;2022-08-04
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