Hereditary Spherocytosis Latest Advances

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

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

When a Trait Becomes a Disease: A Rare Hematologic Overlap of Sickle Cell Trait and Hereditary Spherocytosis.

Journal: American journal of hematology

Published: October 10, 2025

Exchange Transfusion via Peripheral Access for Neonate With Hyperbilirubinemia and Hereditary Spherocytosis in the NICU: A Case Report.

Journal: Advances in neonatal care : official journal of the National Association of Neonatal Nurses

Published: October 07, 2025

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Journal: Fetal and pediatric pathology

Published: September 27, 2025

Challenging diagnosis of spherocytosis in early infancy.

Journal: BMJ case reports

Published: August 25, 2025

Laparoscopic Subtotal Splenectomy in Pediatric Patients With Hematologic Disorders: A Case Series and Operative Technique.

Journal: Asian journal of endoscopic surgery

Published: July 28, 2025

Hereditary Spherocytosis: Review of Presentation at Birth.

Journal: Children (Basel, Switzerland)

Published: July 27, 2025

A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report.

Journal: Frontiers in pediatrics

Published: July 15, 2025

Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrinLELY in Trans.

Journal: American journal of hematology

Published: July 14, 2025

Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report.

Journal: Frontiers in oncology

Published: July 13, 2025

Role of Additional Erythrocyte and Reticulocyte Parameters Offered by Sysmex XN-9000 in the Diagnostic Workup of Hereditary Spherocytosis: A New Screening Algorithm According to Age.

Journal: International journal of laboratory hematology

Published: July 01, 2025

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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.

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.

When a Trait Becomes a Disease: A Rare Hematologic Overlap of Sickle Cell Trait and Hereditary Spherocytosis.

When a Trait Becomes a Disease: A Rare Hematologic Overlap of Sickle Cell Trait and Hereditary Spherocytosis.

Exchange Transfusion via Peripheral Access for Neonate With Hyperbilirubinemia and Hereditary Spherocytosis in the NICU: A Case Report.

Exchange Transfusion via Peripheral Access for Neonate With Hyperbilirubinemia and Hereditary Spherocytosis in the NICU: A Case Report.

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile.

Challenging diagnosis of spherocytosis in early infancy.

Challenging diagnosis of spherocytosis in early infancy.

Laparoscopic Subtotal Splenectomy in Pediatric Patients With Hematologic Disorders: A Case Series and Operative Technique.

Laparoscopic Subtotal Splenectomy in Pediatric Patients With Hematologic Disorders: A Case Series and Operative Technique.

Hereditary Spherocytosis: Review of Presentation at Birth.

Hereditary Spherocytosis: Review of Presentation at Birth.

A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report.

A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report.

Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrinLELY in Trans.

Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrinLELY in Trans.

Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report.

Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report.

Role of Additional Erythrocyte and Reticulocyte Parameters Offered by Sysmex XN-9000 in the Diagnostic Workup of Hereditary Spherocytosis: A New Screening Algorithm According to Age.

Role of Additional Erythrocyte and Reticulocyte Parameters Offered by Sysmex XN-9000 in the Diagnostic Workup of Hereditary Spherocytosis: A New Screening Algorithm According to Age.