Giovanni Ivaldi

Genoa, Italy

Last Updated: 09/26/2026

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Found 14 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).

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.

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

Screening for sickle cell disease: focus on newborn investigations.

Screening for sickle cell disease: focus on newborn investigations.

Journal: Clinical chemistry and laboratory medicine

Published: April 17, 2024

Evolution of acquired haemoglobin H disease monitored by capillary electrophoresis: a case of a myelofibrotic patient with a novel ATRX mutation.

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

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.

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.

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 A2 and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene.

Hemoglobin A2 and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene.

Journal: Genes

Published: October 22, 2021

Hemoglobin Yamagata [β132(H10)Lys→Asn; (HBB: c.399A>T)]: a mosaic to be put together.

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

Hb A2-Pistoia [δ89(F5)Ser→Asn, HBD: c.269G>a]: a Novel Mutation on the δ-Globin Gene in an Italian Child.

Hb A2-Pistoia [δ89(F5)Ser→Asn, HBD: c.269G>a]: a Novel Mutation on the δ-Globin Gene in an Italian Child.

Journal: Hemoglobin

Published: September 11, 2020

Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.

Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.

Journal: Hemoglobin

Published: May 16, 2019

Equipment, staffing, and provision of radiotherapy in Lombardy, Italy: Results of three surveys performed between 2012 and 2016.

Equipment, staffing, and provision of radiotherapy in Lombardy, Italy: Results of three surveys performed between 2012 and 2016.

Journal: Tumori

Published: July 11, 2018

Serendipitous detection of Hemoglobin G-Ferrara variant with Sysmex DIFF channel.

Serendipitous detection of Hemoglobin G-Ferrara variant with Sysmex DIFF channel.

Journal: Clinical biochemistry

Published: July 23, 2015

Showing 1-12 of 14

Last Updated: 09/26/2026