Search

Author/Creator Maiorana, Arianna

1. Dietary lipids in glycogen storage disease type III: A systematic literature study, case studies, and future recommendations. Issue 4 (26th February 2020)

Authors:
Rossi, Alessandro; Hoogeveen, Irene J.; Bastek, Vanessa B.; de Boer, Foekje; Montanari, Chiara; Meyer, Uta; Maiorana, Arianna; Bordugo, Andrea; Dianin, Alice; Campana, Carmen; Rigoldi, Miriam; Kishnani, Priya S.; Pendyal, Surekha; Strisciuglio, Pietro; Gasperini, Serena; Parenti, Giancarlo; Parin...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 43:Issue 4(2020)
Page Start:
770
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening. (30th January 2014)

Authors:
Maiorana, Arianna; Barbetti, Fabrizio; Boiani, Arianna; Rufini, Vittoria; Pizzoferro, Milena; Francalanci, Paola; Faletra, Flavio; Nichols, Colin G.; Grimaldi, Chiara; de Ville de Goyet, Jean; Rahier, Jacques; Henquin, Jean‐Claude; Dionisi‐Vici, Carlo
Journal:
Clinical endocrinology
Issue:
Volume 81:Number 5(2014:Nov.)
Page Start:
679
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Plasma methylcitric acid and its correlations with other disease biomarkers: The impact in the follow up of patients with propionic and methylmalonic acidemia. Issue 6 (23rd August 2020)

Authors:
Maines, Evelina; Catesini, Giulio; Boenzi, Sara; Mosca, Antonella; Candusso, Manila; Dello Strologo, Luca; Martinelli, Diego; Maiorana, Arianna; Liguori, Alessandra; Olivieri, Giorgia; Taurisano, Roberta; Piemonte, Fiorella; Rizzo, Cristiano; Spada, Marco; Dionisi‐Vici, Carlo
Journal:
Journal of inherited metabolic disease
Issue:
Volume 43:Issue 6(2020)
Page Start:
1173
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Uniparental isodisomy of chromosome 1 results in glycogen storage disease type III with profound growth retardation. Issue 5 (27th March 2019)

Authors:
Ponzi, Emanuela; Alesi, Viola; Lepri, Francesca R.; Genovese, Silvia; Loddo, Sara; Mucciolo, Mafalda; Novelli, Antonio; Dionisi‐Vici, Carlo; Maiorana, Arianna
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 5(2019)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗