SPTA1-Related Hereditary Spherocytosis: Novel Compound Heterozygous Mutations With Severe Clinical Manifestation. [PDF]
Khor J, Boo YL.
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Case Report: Post-splenectomy bulky pelvic splenosis in an adolescent with hereditary spherocytosis. [PDF]
Di Majo BE +11 more
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Splenic Artery Embolization as a Primary Treatment for Hereditary Spherocytosis: A Case Report. [PDF]
Mahamat HA +5 more
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Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous <i>SPTA1</i> Variant and Hepatic Fibrosis [PDF]
Koçak Göl D +6 more
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Three novel heterozygous ANK1 loss-of-function variants cause hereditary spherocytosis in Chinese families. [PDF]
Wang Y +8 more
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Genetic screening strategy for children with hereditary spherocytosis in Jiangxi Province of China. [PDF]
Wu C, Xu Z, Wan Q, Chen F, Ye Y, Wang H.
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Transcatheter edge-to-edge repair for post-surgical recurrent mitral regurgitation in hereditary spherocytosis: a case report. [PDF]
Yagasaki H +4 more
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Clinical characteristics of hereditary spherocytosis with red blood cell membrane protein gene variants. [PDF]
Cheng J +4 more
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Drug-induced liver injury from Deferasirox in a pediatric patient with hereditary spherocytosis: A case report. [PDF]
Talwar S +5 more
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Red cell shape regulation by band 3-ankyrin-spectrin linkage: implications for clinical severity of bovine hereditary spherocytosis. [PDF]
Miyazono K +13 more
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