Elisa Ferro

Via Consolare Valeria, 1
Messina, 98125, Italy

Last Updated: 09/26/2026

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Found 11 publications

Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion.

Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion.

Journal: Pediatric surgery international

Published: May 14, 2018

FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family.

FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: February 11, 2018

Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study.

Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study.

Journal: Cytokine

Published: December 19, 2017

Co-inheritance of HBB:c.-106G > C, a rare single nucleotide variation at position -56 relative to transcription initiation site, with other known mutations in the globin clusters.

Co-inheritance of HBB:c.-106G > C, a rare single nucleotide variation at position -56 relative to transcription initiation site, with other known mutations in the globin clusters.

Journal: Hematology (Amsterdam, Netherlands)

Published: November 22, 2017

A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype.

A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype.

Journal: Hematology (Amsterdam, Netherlands)

Published: April 28, 2017

Inflammatory biomarkers and intellectual disability in patients with Down syndrome.

Inflammatory biomarkers and intellectual disability in patients with Down syndrome.

Journal: Journal of intellectual disability research : JIDR

Published: February 02, 2017

Genotoxic effect of iron overload and disease complications in transfused β thalassaemic patients.

Genotoxic effect of iron overload and disease complications in transfused β thalassaemic patients.

Journal: Mutagenesis

Published: December 10, 2016

The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients.

The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients.

Journal: Hematology (Amsterdam, Netherlands)

Published: November 02, 2016

Soluble hemojuvelin in transfused and untransfused thalassaemic subjects.

Soluble hemojuvelin in transfused and untransfused thalassaemic subjects.

Journal: European journal of haematology

Published: July 16, 2016

HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients.

HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients.

Journal: British journal of haematology

Published: October 13, 2015

Oxidative damage and genotoxicity biomarkers in transfused and untransfused thalassemic subjects.

Oxidative damage and genotoxicity biomarkers in transfused and untransfused thalassemic subjects.

Journal: Free radical biology & medicine

Published: March 05, 2012

Showing 1-11 of 11

Last Updated: 09/26/2026