Arianna Maiorana

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 11

Top Topics

Transition Metal

Fluorescence Imaging

Top Venues

Orphanet journal of rare diseases

Journal of inherited metabolic disease

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Evelina Maines, Michele Moretti, Nicola Vitturi, Giorgia Gugelmo, Ilaria Fasan, Livia Lenzini, Giovanni Piccoli, Vincenza Gragnaniello, Arianna Maiorana, Massimo Soffiati, Alberto B Burlina, Roberto Franceschi
Understanding the Pathogenesis of Cardiac Complications in Patients with Propionic Acidemia and Exploring Therapeutic Alternatives for Those Who Are Not Eligible or Are Waiting for Liver Transplantation. Metabolites 13 (4) (2023)
Evelina Maines, Michele Moretti, Nicola Vitturi, Giorgia Gugelmo, Ilaria Fasan, Livia Lenzini, Giovanni Piccoli, Vincenza Gragnaniello, Arianna Maiorana, Massimo Soffiati, Alberto B Burlina, Roberto Franceschi
Understanding the Pathogenesis of Cardiac Complications in Patients with Propionic Acidemia and Exploring Therapeutic Alternatives for Those Who Are Not Eligible or Are Waiting for Liver Transplantation. Metabolites 13 (4) (2023)
Evelina Maines, Michele Moretti, Nicola Vitturi, Giorgia Gugelmo, Ilaria Fasan, Livia Lenzini, Giovanni Piccoli, Vincenza Gragnaniello, Arianna Maiorana, Massimo Soffiati, Alberto B Burlina, Roberto Franceschi
Understanding the Pathogenesis of Cardiac Complications in Patients with Propionic Acidemia and Exploring Therapeutic Alternatives for Those Who Are Not Eligible or Are Waiting for Liver Transplantation. Metabolites 13 (4) (2023)
Evelina Maines, Michele Moretti, Nicola Vitturi, Giorgia Gugelmo, Ilaria Fasan, Livia Lenzini, Giovanni Piccoli, Vincenza Gragnaniello, Arianna Maiorana, Massimo Soffiati, Alberto B Burlina, Roberto Franceschi
Understanding the Pathogenesis of Cardiac Complications in Patients with Propionic Acidemia and Exploring Therapeutic Alternatives for Those Who Are Not Eligible or Are Waiting for Liver Transplantation. Metabolites 13 (4) (2023)
Francesco Tagliaferri, Miriam Massese, Luisa Russo, Anna Commone, Serena Gasperini, Roberta Pretese, Carlo Dionisi-Vici, Arianna Maiorana
Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohort. Orphanet journal of rare diseases 17 (1) (2022)
Miriam Massese, Francesco Tagliaferri, Carlo Dionisi-Vici, Arianna Maiorana
Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI. Orphanet journal of rare diseases 17 (1) (2022)
Arianna Maiorana, Stefania Caviglia, Benedetta Greco, Paolo Alfieri, Francesca Cumbo, Carmen Campana, Silvia Maria Bernabei, Raffaella Cusmai, Antonella Mosca, Carlo Dionisi-Vici
Ketogenic diet as elective treatment in patients with drug-unresponsive hyperinsulinemic hypoglycemia caused by glucokinase mutations. Orphanet journal of rare diseases 16 (1) (2021)
Evelina Maines, Giulio Catesini, Sara Boenzi, Antonella Mosca, Manila Candusso, Luca Dello Strologo, Diego Martinelli, Arianna Maiorana, Alessandra Liguori, Giorgia Olivieri, Roberta Taurisano, Fiorella Piemonte, Cristiano Rizzo, Marco Spada, Carlo Dionisi-Vici
Plasma methylcitric acid and its correlations with other disease biomarkers: The impact in the follow up of patients with propionic and methylmalonic acidemia. Journal of inherited metabolic disease 43 (6) (2020)
Arianna Maiorana, Antonella Sabia, Tiziana Corsetti, Carlo Dionisi-Vici
Safety of vaccines administration in hereditary fructose intolerance. Orphanet journal of rare diseases 15 (1) (2020)
Emanuela Ponzi, Viola Alesi, Francesca Romana Lepri, Silvia Genovese, Sara Loddo, Mafalda Mucciolo, Antonio Novelli, Carlo Dionisi-Vici, Arianna Maiorana
Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardation. Molecular genetics & genomic medicine 7 (5) (2019)
Arianna Maiorana, Carlo Dionisi-Vici
Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties. Journal of inherited metabolic disease 40 (4) (2017)