Elisa Fermo

Via Francesco Sforza, 35
Milan, 20122, Italy

Last Updated: 09/26/2026

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Found 64 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

Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With Erythrocytosis.

Characterization of a Newly Discovered Non-Coding Variant in the EPO Gene Identified in Two Unrelated Italian Pedigrees With Erythrocytosis.

Journal: American journal of hematology

Published: October 31, 2025

Hypomorphic ATP11c is a novel regulator of decreased efficacy of transfused red blood cells in humans and mice.

Hypomorphic ATP11c is a novel regulator of decreased efficacy of transfused red blood cells in humans and mice.

Journal: HemaSphere

Published: October 07, 2025

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

Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literature.

Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literature.

Journal: Orphanet journal of rare diseases

Published: September 23, 2024

Recessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant.

Recessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant.

Journal: Clinical pediatrics

Published: March 05, 2024

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

Immunomodulatory cytokines and clonal dynamics in low-risk myelodysplastic syndromes patients treated with luspatercept.

Immunomodulatory cytokines and clonal dynamics in low-risk myelodysplastic syndromes patients treated with luspatercept.

Journal: American journal of hematology

Published: June 30, 2023

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

Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.

Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation.

Journal: Pediatric blood & cancer

Published: March 03, 2023

Showing 1-12 of 64

Last Updated: 09/26/2026