Olivieri G - Search Results

1

The diagnostic challenge of mild citrulline elevation at newborn screening.

Siri B, Olivieri G, Angeloni A, Cairoli S, Carducci C, Cotugno G, Di Michele S, Giovanniello T, La Marca G, Lepri FR, Novelli A, Rossi C, Semeraro M, Dionisi-Vici C. Siri B, et al. Among authors: olivieri g. Mol Genet Metab. 2022 Apr;135(4):327-332. doi: 10.1016/j.ymgme.2022.02.008. Epub 2022 Feb 20. Mol Genet Metab. 2022. PMID: 35279366

2

Persistent Hypoglycemia in Children: Targeted Gene Panel Improves the Diagnosis of Hypoglycemia Due to Inborn Errors of Metabolism.

Ponzi E, Maiorana A, Lepri FR, Mucciolo M, Semeraro M, Taurisano R, Olivieri G, Novelli A, Dionisi-Vici C. Ponzi E, et al. Among authors: olivieri g. J Pediatr. 2018 Nov;202:272-278.e4. doi: 10.1016/j.jpeds.2018.06.050. Epub 2018 Sep 5. J Pediatr. 2018. PMID: 30193751

3

Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia.

Olivieri G, Pro S, Diodato D, Di Capua M, Longo D, Martinelli D, Bertini E, Dionisi-Vici C. Olivieri G, et al. Orphanet J Rare Dis. 2019 Aug 23;14(1):208. doi: 10.1186/s13023-019-1181-7. Orphanet J Rare Dis. 2019. PMID: 31443672 Free PMC article.

4

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

Semeraro M, Sacchetti E, Deodato F, Coşkun T, Lay I, Catesini G, Olivieri G, Rizzo C, Boenzi S, Dionisi-Vici C. Semeraro M, et al. Among authors: olivieri g. Orphanet J Rare Dis. 2021 Jan 9;16(1):24. doi: 10.1186/s13023-020-01662-8. Orphanet J Rare Dis. 2021. PMID: 33422100 Free PMC article.

5

Ethylmalonic encephalopathy and liver transplantation: long-term outcome of the first treated patient.

Olivieri G, Martinelli D, Longo D, Grimaldi C, Liccardo D, Di Meo I, Pietrobattista A, Sidorina A, Semeraro M, Dionisi-Vici C. Olivieri G, et al. Orphanet J Rare Dis. 2021 May 19;16(1):229. doi: 10.1186/s13023-021-01867-5. Orphanet J Rare Dis. 2021. PMID: 34011365 Free PMC article.

6

The urinary organic acids profile in single large-scale mitochondrial DNA deletion disorders.

Semeraro M, Boenzi S, Carrozzo R, Diodato D, Martinelli D, Olivieri G, Antonetti G, Sacchetti E, Catesini G, Rizzo C, Dionisi-Vici C. Semeraro M, et al. Among authors: olivieri g. Clin Chim Acta. 2018 Jun;481:156-160. doi: 10.1016/j.cca.2018.03.002. Epub 2018 Mar 10. Clin Chim Acta. 2018. PMID: 29534959

7

Early neurodevelopmental characterization in children with cobalamin C/defect.

Ricci D, Martinelli D, Ferrantini G, Lucibello S, Gambardella M, Olivieri G, Chieffo D, Battaglia D, Diodato D, Iarossi G, Donati AM, Dionisi-Vici C, Battini R, Mercuri EM. Ricci D, et al. Among authors: olivieri g. J Inherit Metab Dis. 2020 Mar;43(2):367-374. doi: 10.1002/jimd.12171. Epub 2020 Jan 16. J Inherit Metab Dis. 2020. PMID: 31503356

8

Plasma methylcitric acid and its correlations with other disease biomarkers: The impact in the follow up of patients with propionic and methylmalonic acidemia.

Maines E, Catesini G, Boenzi S, Mosca A, Candusso M, Dello Strologo L, Martinelli D, Maiorana A, Liguori A, Olivieri G, Taurisano R, Piemonte F, Rizzo C, Spada M, Dionisi-Vici C. Maines E, et al. Among authors: olivieri g. J Inherit Metab Dis. 2020 Nov;43(6):1173-1185. doi: 10.1002/jimd.12287. Epub 2020 Aug 23. J Inherit Metab Dis. 2020. PMID: 32681732

9

Orofacial features and pediatric dentistry in the long-term management of Infantile Pompe Disease children.

Galeotti A, De Rosa S, Uomo R, Dionisi-Vici C, Deodato F, Taurisano R, Olivieri G, Festa P. Galeotti A, et al. Among authors: olivieri g. Orphanet J Rare Dis. 2020 Nov 23;15(1):329. doi: 10.1186/s13023-020-01615-1. Orphanet J Rare Dis. 2020. PMID: 33228748 Free PMC article.

10

Axonal peripheral neuropathy in propionic acidemia: A severe side effect of long-term metronidazole therapy.

Diodato D, Olivieri G, Pro S, Maiorani D, Martinelli D, Deodato F, Taurisano R, Di Capua M, Dionisi-Vici C. Diodato D, et al. Among authors: olivieri g. Neurology. 2018 Sep 18;91(12):565-567. doi: 10.1212/WNL.0000000000006209. Epub 2018 Aug 17. Neurology. 2018. PMID: 30120134 No abstract available.

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