Natascia Campostrini

Verona, 37134, Italy

Last Updated: 09/26/2026

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Found 24 publications

A Gain-of-Function Mutation on BCKDK Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid Metabolism.

A Gain-of-Function Mutation on BCKDK Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid Metabolism.

Journal: Genes

Published: December 21, 2021

Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy.

Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy.

Journal: Frontiers in pediatrics

Published: January 30, 2021

Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience.

Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience.

Journal: Molecular genetics and metabolism reports

Published: June 30, 2020

High-protein goat's milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice.

High-protein goat's milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice.

Journal: Public health nutrition

Published: July 25, 2017

A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients?

A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients?

Journal: Journal of nephrology

Published: December 08, 2016

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity.

Journal: Journal of inherited metabolic disease

Published: October 12, 2016

Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient.

Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient.

Journal: JIMD reports

Published: September 12, 2016

Toward Worldwide Hepcidin Assay Harmonization: Identification of a Commutable Secondary Reference Material.

Toward Worldwide Hepcidin Assay Harmonization: Identification of a Commutable Secondary Reference Material.

Journal: Clinical chemistry

Published: March 08, 2016

Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.

Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.

Journal: American journal of hematology

Published: December 09, 2015

Detection of a rare mutation in the ferroportin gene through targeted next generation sequencing.

Detection of a rare mutation in the ferroportin gene through targeted next generation sequencing.

Journal: Blood transfusion = Trasfusione del sangue

Published: October 29, 2015

Serum Hepcidin and Iron Absorption in Paediatric Inflammatory Bowel Disease.

Serum Hepcidin and Iron Absorption in Paediatric Inflammatory Bowel Disease.

Journal: Journal of Crohn's & colitis

Published: July 20, 2015

Does TMPRSS6 RS855791 polymorphism contribute to iron deficiency in treated celiac disease?

Does TMPRSS6 RS855791 polymorphism contribute to iron deficiency in treated celiac disease?

Journal: The American journal of gastroenterology

Published: January 09, 2015

Showing 1-12 of 24

Last Updated: 09/26/2026