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Last Updated: 10/31/2025

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Found 2668 publications

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.

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.

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.

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.

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.

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.

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.

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

Journal: American journal of hematology
Published: July 14, 2025

Combined hereditary spherocytosis and β-thalassaemia trait: A rare co-existence.

Combined hereditary spherocytosis and β-thalassaemia trait: A rare co-existence.

Journal: The National medical journal of India
Published: June 30, 2025

Hereditary spherocytosis in a neonate during cardiac surgery.

Hereditary spherocytosis in a neonate during cardiac surgery.

Journal: Perfusion
Published: June 29, 2025

Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children.

Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children.

Journal: Frontiers in pediatrics
Published: June 19, 2025

Diagnosis and management of severe SPTA1-associated congenital anaemia in a family cohort affected by two founder variants.

Diagnosis and management of severe SPTA1-associated congenital anaemia in a family cohort affected by two founder variants.

Journal: BMJ case reports
Published: May 12, 2025

A case report of hereditary spherocytosis complicated by massive splenomegaly and cholelithiasis.

A case report of hereditary spherocytosis complicated by massive splenomegaly and cholelithiasis.

Journal: Journal of surgical case reports
Published: May 09, 2025
Showing 1-12 of 2,668

Last Updated: 10/31/2025