Hereditary Spherocytosis Latest Advances

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.

Journal: Clinical laboratory

Published: April 07, 2026

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

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: February 19, 2026

Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: February 02, 2026

Sacral Brodie's abscess in a patient with hereditary spherocytosis.

Journal: BMJ case reports

Published: January 16, 2026

Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.

Journal: Hemoglobin

Published: December 21, 2025

Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review.

Journal: International journal of molecular sciences

Published: December 08, 2025

Correction: Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis.

Journal: Frontiers in genetics

Published: December 07, 2025

Establishing a Reference Interval for Flow Cytometric Analysis of Red Blood Cell Osmotic Fragility in a Healthy Korean Population.

Journal: Annals of clinical and laboratory science

Published: November 18, 2025

Parvovirus B19-Induced Aplastic Crisis and Hemophagocytic Lymphohistiocytosis in a Child With Hereditary Spherocytosis.

Journal: Cureus

Published: November 17, 2025

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Journal: Cureus

Published: October 31, 2025

Hereditary Spherocytosis Latest Advances

Find the Latest Research About Hereditary Spherocytosis

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

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

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.

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.

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

Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression.

Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression.

Sacral Brodie's abscess in a patient with hereditary spherocytosis.

Sacral Brodie's abscess in a patient with hereditary spherocytosis.

Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.

Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child.

Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review.

Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review.

Correction: Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis.

Correction: Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis.

Establishing a Reference Interval for Flow Cytometric Analysis of Red Blood Cell Osmotic Fragility in a Healthy Korean Population.

Establishing a Reference Interval for Flow Cytometric Analysis of Red Blood Cell Osmotic Fragility in a Healthy Korean Population.

Parvovirus B19-Induced Aplastic Crisis and Hemophagocytic Lymphohistiocytosis in a Child With Hereditary Spherocytosis.

Parvovirus B19-Induced Aplastic Crisis and Hemophagocytic Lymphohistiocytosis in a Child With Hereditary Spherocytosis.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.

Confounding Factors in the Diagnosis of Hereditary Spherocytosis and Gallstone Formation in Related Hemolytic Disorders From a Tertiary Care Center in North India.