Carlo Dionisi-Vici

Head of the Division

Ospedale Pediatrico Bambino Gesù

Italy

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About

Carlo Dionisi-Vici is the Head of the Division at Ospedale Pediatrico Bambino Gesù in Italy. His research focuses on pediatric metabolic disorders, including cystic fibrosis, tyrosinemia, and lysosomal storage disorders. He has contributed significantly to the development of diagnostic methods and treatment interventions for inherited metabolic conditions. His recent publications reflect a commitment to improving early detection and patient care in pediatric populations.

Articles (15)

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2025

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2025

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2025

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2024

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2024

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2024

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2022

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2022

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2022

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2021

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2021

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2021

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2021

Collaborators (16)

Manoe Janssen

Assistant professor

Utrecht University

NETHERLANDS

Carlo Dionisi-Vici

Research Interests

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Articles (15)

Single Amino Acid Supplementation in Inherited Metabolic Disorders: An Evidence-Based Review of Interventions

Development and Validation of a New LC-MS/MS Method for Simultaneous Quantification of Ivacaftor, Tezacaftor and Elexacaftor Plasma Levels in Pediatric Cystic Fibrosis Patients

Integrating Machine Learning and Follow-Up Variables to Improve Early Detection of Hepatocellular Carcinoma in Tyrosinemia Type 1: A Multicenter Study

Measurement of Anti-TNF Biologics in Serum Samples of Pediatric Patients: Comparison of Enzyme-Linked Immunosorbent Assay (ELISA) with a Rapid and Automated Fluorescence-Based Lateral Flow Immunoassay

Propionic Acidemia, Methylmalonic Acidemia, and Cobalamin C Deficiency: Comparison of Untargeted Metabolomic Profiles

Pharmacokinetic Evaluation of Oral Viscous Budesonide in Paediatric Patients with Eosinophilic Oesophagitis in Repaired Oesophageal Atresia

The Unmet Needs of Lysosomal Storage Disorders from Early Diagnosis to Caregiving Pathways: An Italian Perspective

A New Pattern of Brain and Cord Gadolinium Enhancement in Molybdenum Cofactor Deficiency: A Case Report

Expanded Newborn Screening in Italy Using Tandem Mass Spectrometry: Two Years of National Experience

High Incidence of Partial Biotinidase Deficiency in the First 3 Years of a Regional Newborn Screening Program in Italy

Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis

Partial Biotinidase Deficiency Revealed Imbalances in Acylcarnitines Profile at Tandem Mass Spectrometry Newborn Screening

Benefits and toxicity of disulfiram in preclinical models of nephropathic cystinosis

ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype

A new UHPLC-MS/MS method for the screening of urinary oligosaccharides expands the detection of storage disorders

Collaborators (16)

Manoe Janssen

amelia morrone

Elvira Verduci

silvia di michele

Sebastiano A.G. Lava

Damiana Pieragostino

Claudia Rossi

Giulia Frisso

Margherita RUOPPOLO

FRANCESCA NARDECCHIA

Susan Berry

Ines Bucci

alessandro salina

Marco Spada

Alberto B. Burlina

Sara Verrocchio

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