Sauro Maoggi
Florence, Italy
Last Updated: 09/26/2026
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Found 8 publications
Familial erythrocytosis and phenotypic heterogeneity associated with different defects in alpha globin genes: a significant new case of Hb Wroclaw (α88(F9) Ala>Glu; HBA1: c.266C>A).
Journal: Clinical chemistry and laboratory medicine
Published: August 25, 2025
Hb A2-Pontedera [δ93(F9) Cys > Trp; HBD: C.282T > G]: A New δ-Globin Chain Variant Detected by Screening Tests for Hemoglobinopathies.
Journal: Hemoglobin
Published: December 17, 2024
Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel ATRX mutation.
Journal: Clinical chemistry and laboratory medicine
Published: April 12, 2024
Ability of the Capillary Electrophoresis-based HbA1c Assay to Detect Rare Hemoglobin Variants.
Journal: Annals of laboratory medicine
Published: April 09, 2024
Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary Electrophoresis.
Journal: Hemoglobin
Published: September 15, 2022
Two co-inherited hemoglobin variants revealed by capillary electrophoresis during quantification of glycated hemoglobin.
Journal: Clinical chemistry and laboratory medicine
Published: November 28, 2021
Hemoglobin Yamagata [β132(H10)Lys→Asn; (HBB: c.399A>T)]: a mosaic to be put together.
Journal: Clinical chemistry and laboratory medicine
Published: March 28, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026