Hereditary Spherocytosis Latest Advances

Find the Latest Research About Hereditary Spherocytosis

Last Updated: 06/30/2026

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Found 2709 publications

Red cell shape regulation by band 3-ankyrin-spectrin linkage: implications for clinical severity of bovine hereditary spherocytosis.

Red cell shape regulation by band 3-ankyrin-spectrin linkage: implications for clinical severity of bovine hereditary spherocytosis.

Journal: Blood. Red cells & iron
Published: June 04, 2026

Hereditary Hemolytic Spherocytosis in the Active-Duty Population: A Unique Case.

Hereditary Hemolytic Spherocytosis in the Active-Duty Population: A Unique Case.

Journal: Cureus
Published: May 19, 2026

Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report.

Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report.

Journal: Cureus
Published: April 16, 2026

Robot-Assisted Laparoscopic Splenectomy In Children: A Case Report with Literature Review.

Robot-Assisted Laparoscopic Splenectomy In Children: A Case Report with Literature Review.

Journal: Journal of visualized experiments : JoVE
Published: April 13, 2026

Abnormal Liver Function with Low Glycated Hemoglobin: a Case of Hereditary Spherocytosis Concealed by Liver Disease Symptoms.

Abnormal Liver Function with Low Glycated Hemoglobin: a Case of Hereditary Spherocytosis Concealed by Liver Disease Symptoms.

Journal: Clinical laboratory
Published: April 07, 2026

Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis

Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: March 16, 2026

Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care.

Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care.

Journal: Prenatal diagnosis
Published: March 11, 2026

Evaluation of the Eosin-5'-Maleimide Flow Cytometry Test for the Diagnosis of Hereditary Spherocytosis.

Evaluation of the Eosin-5'-Maleimide Flow Cytometry Test for the Diagnosis of Hereditary Spherocytosis.

Journal: European journal of haematology
Published: February 27, 2026

De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review.

De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review.

Journal: Annals of hematology
Published: February 25, 2026

Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous SPTA1 Variant and Hepatic Fibrosis

Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous SPTA1 Variant and Hepatic Fibrosis

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology
Published: February 19, 2026

Internalizing and Externalizing Problems and Psychiatric Comorbidities in Children With Hereditary Spherocytosis.

Internalizing and Externalizing Problems and Psychiatric Comorbidities in Children With Hereditary Spherocytosis.

Journal: Journal of pediatric hematology/oncology
Published: February 18, 2026

Diagnostic performance of flow cytometric osmotic fragility testing in hereditary spherocytosis.

Diagnostic performance of flow cytometric osmotic fragility testing in hereditary spherocytosis.

Journal: Cytometry. Part B, Clinical cytometry
Published: February 15, 2026
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Last Updated: 06/30/2026