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Last Updated: 10/31/2025
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Found 141 publications
Homozygous α-Spectrin (SPTA1) Variant Causing Persistent Hereditary Pyropoikilocytosis in a Newborn: A Case Report and Literature Review.
Journal: International medical case reports journal
Published: May 19, 2025
Challenges in determining red blood cell and platelet counts in severely burned patients
Journal: Orvosi hetilap
Published: May 08, 2025
Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis.
Journal: Prenatal diagnosis
Published: January 30, 2025
Genetic mutations of congenital red cell membrane defects in hydrops fetalis.
Journal: Fetal diagnosis and therapy
Published: December 28, 2024
Genetic Mutations of Congenital Red Cell Membrane Defects in Hydrops Fetalis.
Journal: Fetal diagnosis and therapy
Published: December 28, 2024
Hereditary pyropoikilocytosis resulting in artefactual thrombocytosis.
Journal: British journal of haematology
Published: November 07, 2024
Hereditary Pyropoikilocytosis as a Modifier of Sickle Cell Disease Severity.
Journal: Journal of pediatric hematology/oncology
Published: September 18, 2024
Placental Histopathologic Findings in Fetal Hereditary Pyropoikilocytosis after Undergoing Successful Intrauterine Transfusion.
Journal: Fetal and pediatric pathology
Published: December 18, 2023
One-step amplification refractory mutation system-PCR/high-resolution melting curve assay for carrier detection of red blood cell membranopathy caused by common SPTB mutations.
Journal: International journal of laboratory hematology
Published: July 06, 2023
Homozygous SPTA1-associated hereditary pyropoikilocytosis presenting as hydrops fetalis.
Journal: Transfusion
Published: May 15, 2023
Last Updated: 10/31/2025