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Author/Creator Mattiuzzo, Matteo

1. Clinical presentation and molecular characterization of a novel patient with variant POC1A‐related syndrome. Issue 4 (13th January 2021)

Authors:
Majore, Silvia; Agolini, Emanuele; Micale, Lucia; Pascolini, Giulia; Zuppi, Paolo; Cocciadiferro, Dario; Morlino, Silvia; Mattiuzzo, Matteo; Valiante, Michele; Castori, Marco; Novelli, Antonio; Grammatico, Paola
Journal:
Clinical genetics
Issue:
Volume 99:Issue 4(2021)
Page Start:
540
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis. Issue 4 (7th May 2022)

Authors:
Tummolo, Albina; Leone, Piero; Tolomeo, Maria; Solito, Rita; Mattiuzzo, Matteo; Lepri, Francesca Romana; Lorè, Tania; Cardinali, Roberta; De Giovanni, Donatella; Simonetti, Simonetta; Barile, Maria
Journal:
JIMD reports
Issue:
Volume 63:Issue 4(2022)
Page Start:
276
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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