Cristina Vercellati

Via Francesco Sforza, 35
Milan, 20122, Italy

Last Updated: 09/26/2026

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Found 29 publications

Decoding the Ektacytometric Landscape of Hereditary Spherocytosis: Insights from 204 Cases.

Decoding the Ektacytometric Landscape of Hereditary Spherocytosis: Insights from 204 Cases.

Journal: Diagnostics (Basel, Switzerland)

Published: April 30, 2026

Integrated enzymatic and molecular diagnosis of G6PD deficiency: a one-year experience identifying five novel variants.

Integrated enzymatic and molecular diagnosis of G6PD deficiency: a one-year experience identifying five novel variants.

Journal: Annals of hematology

Published: April 07, 2026

Rheological and biochemical comparison of cord and adult blood red cells for transfusion applications.

Rheological and biochemical comparison of cord and adult blood red cells for transfusion applications.

Journal: Scientific reports

Published: October 07, 2025

Not-So-Rare Defects of RBC Lipidic Composition: Four New Cases of Flippase Deficiency Due to ATP11C Mutations.

Not-So-Rare Defects of RBC Lipidic Composition: Four New Cases of Flippase Deficiency Due to ATP11C Mutations.

Journal: International journal of molecular sciences

Published: July 04, 2025

Glycolytic activity and in vitro effect of the pyruvate kinase activator AG-946 in red blood cells from low-risk myelodysplastic syndromes patients: A proof-of-concept study.

Glycolytic activity and in vitro effect of the pyruvate kinase activator AG-946 in red blood cells from low-risk myelodysplastic syndromes patients: A proof-of-concept study.

Journal: American journal of hematology

Published: January 22, 2024

When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms.

When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms.

Journal: British journal of haematology

Published: June 14, 2023

Cytokine polymorphisms in patients with autoimmune hemolytic anemia.

Cytokine polymorphisms in patients with autoimmune hemolytic anemia.

Journal: Frontiers in immunology

Published: May 12, 2023

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.

Journal: Pediatric blood & cancer

Published: March 03, 2023

Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.

Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.

Journal: Scientific reports

Published: November 15, 2022

Case report: Transfusion independence and abolition of extravascular hemolysis in a PNH patient treated with pegcetacoplan.

Case report: Transfusion independence and abolition of extravascular hemolysis in a PNH patient treated with pegcetacoplan.

Journal: Frontiers in immunology

Published: October 03, 2022

Pyruvate Kinase Deficiency: Current Challenges and Future Prospects.

Pyruvate Kinase Deficiency: Current Challenges and Future Prospects.

Journal: Journal of blood medicine

Published: May 31, 2022

Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.

Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.

Journal: Frontiers in physiology

Published: May 20, 2022

Showing 1-12 of 29

Last Updated: 09/26/2026