Hereditary Ovalocytosis Latest Advances

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

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 in a child with an autosomal recessive SPTA1 mutation: a case report from Saudi Arabia.

Journal: Journal of medicine and life

Published: March 05, 2025

Parvovirus B19-induced autoimmune hemolytic anemia in hereditary elliptocytosis.

Journal: Blood

Published: January 02, 2025

Unraveling biochemical differences in the membrane of functional RBCs and elliptocytes using vortex beam-based micro-Raman spectroscopy.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Published: December 18, 2024

Hereditary Pyropoikilocytosis as a Modifier of Sickle Cell Disease Severity.

Journal: Journal of pediatric hematology/oncology

Published: September 18, 2024

A rare case report of hemolysis in a newborn: hereditary elliptocytosis.

Journal: Frontiers in pediatrics

Published: August 23, 2024

Frameshift Mutation in the EPB41 Gene with Hereditary Elliptocytosis.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: May 27, 2024

Effect of Staphylococcal Nuclease and Tudor Domain Containing 1/SLC7A11 on the Occurrence and Development of Osteosarcoma by Inhibiting Ferroptosis

Journal: Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae

Published: March 04, 2024

Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion.

Journal: Fetal and pediatric pathology

Published: December 18, 2023

Effects of Daidzein, Tempeh, and a Probiotic Digested in an Artificial Gastrointestinal Tract on Calcium Deposition in Human Osteoblast-like Saos-2 Cells.

Journal: International journal of molecular sciences

Published: December 06, 2023

Hereditary Ovalocytosis Latest Advances

Find the Latest Research About Hereditary Ovalocytosis

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.

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.

Hereditary elliptocytosis in a child with an autosomal recessive SPTA1 mutation: a case report from Saudi Arabia.

Hereditary elliptocytosis in a child with an autosomal recessive SPTA1 mutation: a case report from Saudi Arabia.

Parvovirus B19-induced autoimmune hemolytic anemia in hereditary elliptocytosis.

Parvovirus B19-induced autoimmune hemolytic anemia in hereditary elliptocytosis.

Unraveling biochemical differences in the membrane of functional RBCs and elliptocytes using vortex beam-based micro-Raman spectroscopy.

Unraveling biochemical differences in the membrane of functional RBCs and elliptocytes using vortex beam-based micro-Raman spectroscopy.

Hereditary Pyropoikilocytosis as a Modifier of Sickle Cell Disease Severity.

Hereditary Pyropoikilocytosis as a Modifier of Sickle Cell Disease Severity.

A rare case report of hemolysis in a newborn: hereditary elliptocytosis.

A rare case report of hemolysis in a newborn: hereditary elliptocytosis.

Frameshift Mutation in the EPB41 Gene with Hereditary Elliptocytosis.

Frameshift Mutation in the EPB41 Gene with Hereditary Elliptocytosis.

Effect of Staphylococcal Nuclease and Tudor Domain Containing 1/SLC7A11 on the Occurrence and Development of Osteosarcoma by Inhibiting Ferroptosis

Effect of Staphylococcal Nuclease and Tudor Domain Containing 1/SLC7A11 on the Occurrence and Development of Osteosarcoma by Inhibiting Ferroptosis

Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion.

Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion.

Effects of Daidzein, Tempeh, and a Probiotic Digested in an Artificial Gastrointestinal Tract on Calcium Deposition in Human Osteoblast-like Saos-2 Cells.

Effects of Daidzein, Tempeh, and a Probiotic Digested in an Artificial Gastrointestinal Tract on Calcium Deposition in Human Osteoblast-like Saos-2 Cells.