Gian L. Forni

Genoa, Italy

Last Updated: 09/26/2026

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Found 119 publications

Non-transfusion-dependent β-thalassemia: A disease of clinical paradoxes.

Non-transfusion-dependent β-thalassemia: A disease of clinical paradoxes.

Journal: Blood reviews

Published: June 28, 2026

Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging.

Colchicine Protects Against Sickle Cell Related Cardiomyopathy: Evidence of the Novel Role of Inflammaging.

Journal: Antioxidants (Basel, Switzerland)

Published: May 18, 2026

The Emerging Role of Liver Stiffness Measurement in Transfusion Dependent Thalassemia.

The Emerging Role of Liver Stiffness Measurement in Transfusion Dependent Thalassemia.

Journal: American journal of hematology

Published: February 18, 2026

Real-world evidence supports the safety and efficacy profile of luspatercept in clinically complex and heavily iron-overloaded patients.

Real-world evidence supports the safety and efficacy profile of luspatercept in clinically complex and heavily iron-overloaded patients.

Journal: British journal of haematology

Published: January 23, 2026

Update of the decision-making algorithm on selecting transfusion-dependent β-thalassemic patients for gene therapy approaches: joint consensus report on behalf of EHA-specialized working group and EBMT hemoglobinopathies working party.

Update of the decision-making algorithm on selecting transfusion-dependent β-thalassemic patients for gene therapy approaches: joint consensus report on behalf of EHA-specialized working group and EBMT hemoglobinopathies working party.

Journal: Bone marrow transplantation

Published: December 23, 2025

Incorporating national disease burden in GBD estimates of haemoglobinopathies in Italy.

Incorporating national disease burden in GBD estimates of haemoglobinopathies in Italy.

Journal: The Lancet. Haematology

Published: November 05, 2025

Iron Overload and Anemia in Transferrin Immune Complex Disease, an Overlooked Monoclonal Gammopathy of Clinical Significance.

Iron Overload and Anemia in Transferrin Immune Complex Disease, an Overlooked Monoclonal Gammopathy of Clinical Significance.

Journal: American journal of hematology

Published: September 30, 2025

Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red blood cell and iron disorders.

Refined classification and phenotype-driven analysis of PIEZO1 variants in hereditary red blood cell and iron disorders.

Journal: Blood

Published: September 11, 2025

Narratives unveil knowledge and awareness-related issue, reinforcing patients' self-identity in sickle cell disease.

Narratives unveil knowledge and awareness-related issue, reinforcing patients' self-identity in sickle cell disease.

Journal: Orphanet journal of rare diseases

Published: August 19, 2025

New insights into mitochondrial segregation from the Doubly Uniparental Inheritance system in bivalves.

New insights into mitochondrial segregation from the Doubly Uniparental Inheritance system in bivalves.

Journal: BMC biology

Published: July 14, 2025

Erratum to: Prevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study.

Erratum to: Prevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study.

Journal: Haematologica

Published: June 01, 2025

Pregnancy and childbirth in women with thalassemia: past and present.

Pregnancy and childbirth in women with thalassemia: past and present.

Journal: Haematologica

Published: April 04, 2025

Showing 1-12 of 119

Last Updated: 09/26/2026