Hereditary Elliptocytosis Latest Advances

Acute Liver Injury with Viral-like Illness and Ceftriaxone Exposure in a Patient with Previously Undiagnosed Hereditary Elliptocytosis.

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

Published: June 19, 2026

Fish-shaped erythrocytes and pincer cells co-occur in distinct hematological disorders and are associated with anemia severity.

Journal: Clinical chemistry and laboratory medicine

Published: June 15, 2026

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.

Journal: BMJ paediatrics open

Published: March 26, 2026

Oxidative stress and antioxidant capacity in hereditary elliptocytosis and hereditary pyropoikilocytosis.

Journal: British journal of haematology

Published: February 25, 2026

Mapping Three Decades of Research on Southeast Asian Ovalocytosis: A Bibliometric Analysis.

Journal: Mediterranean journal of hematology and infectious diseases

Published: February 17, 2026

A βH-spectrin self-interaction domain forms antiparallel dimers that may facilitate non-canonical spectrin membrane skeleton assembly.

Journal: The Journal of biological chemistry

Published: January 28, 2026

Cooley's Legacy Endures-Elliptocytes in X-Linked Sideroblastic Anemia Due to Aminolevulinate Synthase 2 Mutations.

Journal: Pediatric blood & cancer

Published: December 17, 2025

Recurrent Hemolytic Anemia in an Infant with Hereditary Elliptocytosis at a Nigerian Hospital.

Journal: Annals of African medicine

Published: November 25, 2025

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

Journal: Cureus

Published: November 25, 2025

Hereditary red cell defects as an underrecognized cause of neonatal jaundice.

Journal: Journal of perinatology : official journal of the California Perinatal Association

Published: November 12, 2025

Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis.

Journal: International journal of laboratory hematology

Published: July 25, 2025

Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil.

Journal: American journal of hematology

Published: June 05, 2025

Hereditary Elliptocytosis Latest Advances

Find the Latest Research About Hereditary Elliptocytosis

Acute Liver Injury with Viral-like Illness and Ceftriaxone Exposure in a Patient with Previously Undiagnosed Hereditary Elliptocytosis.

Acute Liver Injury with Viral-like Illness and Ceftriaxone Exposure in a Patient with Previously Undiagnosed Hereditary Elliptocytosis.

Fish-shaped erythrocytes and pincer cells co-occur in distinct hematological disorders and are associated with anemia severity.

Fish-shaped erythrocytes and pincer cells co-occur in distinct hematological disorders and are associated with anemia severity.

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.

Oxidative stress and antioxidant capacity in hereditary elliptocytosis and hereditary pyropoikilocytosis.

Oxidative stress and antioxidant capacity in hereditary elliptocytosis and hereditary pyropoikilocytosis.

Mapping Three Decades of Research on Southeast Asian Ovalocytosis: A Bibliometric Analysis.

Mapping Three Decades of Research on Southeast Asian Ovalocytosis: A Bibliometric Analysis.

A βH-spectrin self-interaction domain forms antiparallel dimers that may facilitate non-canonical spectrin membrane skeleton assembly.

A βH-spectrin self-interaction domain forms antiparallel dimers that may facilitate non-canonical spectrin membrane skeleton assembly.

Cooley's Legacy Endures-Elliptocytes in X-Linked Sideroblastic Anemia Due to Aminolevulinate Synthase 2 Mutations.

Cooley's Legacy Endures-Elliptocytes in X-Linked Sideroblastic Anemia Due to Aminolevulinate Synthase 2 Mutations.

Recurrent Hemolytic Anemia in an Infant with Hereditary Elliptocytosis at a Nigerian Hospital.

Recurrent Hemolytic Anemia in an Infant with Hereditary Elliptocytosis at a Nigerian Hospital.

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

Hereditary red cell defects as an underrecognized cause of neonatal jaundice.

Hereditary red cell defects as an underrecognized cause of neonatal jaundice.

Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis.

Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis.

Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil.

Hereditary Elliptocytosis Resulting From Heterozygosity for β Spectrin Tandil.