Works by Olivieri, Giorgia


Results: 25
    1

    Novel NDUFA12 variants are associated with isolated complex I defect and variable clinical manifestation.

    Published in:
    Human Mutation, 2021, v. 42, n. 6, p. 699, doi. 10.1002/humu.24195
    By:
    • Torraco, Alessandra;
    • Nasca, Alessia;
    • Verrigni, Daniela;
    • Pennisi, Alessandra;
    • Zaki, Maha S.;
    • Olivieri, Giorgia;
    • Assouline, Zahra;
    • Martinelli, Diego;
    • Maroofian, Reza;
    • Rizza, Teresa;
    • Di Nottia, Michela;
    • Invernizzi, Federica;
    • Lamantea, Eleonora;
    • Longo, Daniela;
    • Houlden, Henry;
    • Prokisch, Holger;
    • Rötig, Agnès;
    • Dionisi‐Vici, Carlo;
    • Bertini, Enrico;
    • Ghezzi, Daniele
    Publication type:
    Article
    2
    3

    The forward parachute reaction and independent walking in infants with brain lesions.

    Published in:
    Developmental Medicine & Child Neurology, 2011, v. 53, n. 7, p. 636, doi. 10.1111/j.1469-8749.2011.03940.x
    By:
    • ROMEO, DOMENICO M.;
    • RICCI, DANIELA;
    • BARANELLO, GIOVANNI;
    • PAGLIANO, EMANUELA;
    • BROGNA, CLAUDIA;
    • OLIVIERI, GIORGIA;
    • CONTALDO, ILARIA;
    • MAZZONE, DOMENICO;
    • QUINTILIANI, MICHELA;
    • TORRIOLI, MARIA GIULIA;
    • ROMEO, MARIO G.;
    • MERCURI, EUGENIO
    Publication type:
    Article
    4
    5
    6
    7
    8

    The impact of liver transplantation on health‐related quality of life in (acute) intoxication‐type inborn errors of metabolism.

    Published in:
    Journal of Inherited Metabolic Disease, 2023, v. 46, n. 5, p. 906, doi. 10.1002/jimd.12648
    By:
    • Greco, Benedetta;
    • Caviglia, Stefania;
    • Martinelli, Diego;
    • Capitello, Teresa Grimaldi;
    • Liccardo, Daniela;
    • De Nictolis, Francesca;
    • Pietrobattista, Andrea;
    • Huemer, Martina;
    • Piga, Simone;
    • Olivieri, Giorgia;
    • Spagnoletti, Gionata;
    • Spada, Marco;
    • Dionisi‐Vici, Carlo
    Publication type:
    Article
    9

    Neurologic outcome following liver transplantation for methylmalonic aciduria.

    Published in:
    Journal of Inherited Metabolic Disease, 2023, v. 46, n. 3, p. 450, doi. 10.1002/jimd.12599
    By:
    • Martinelli, Diego;
    • Catesini, Giulio;
    • Greco, Benedetta;
    • Guarnera, Alessia;
    • Parrillo, Chiara;
    • Maines, Evelina;
    • Longo, Daniela;
    • Napolitano, Antonio;
    • De Nictolis, Francesca;
    • Cairoli, Sara;
    • Liccardo, Daniela;
    • Caviglia, Stefania;
    • Sidorina, Anna;
    • Olivieri, Giorgia;
    • Siri, Barbara;
    • Bianchi, Roberto;
    • Spagnoletti, Gionata;
    • Dello Strologo, Luca;
    • Spada, Marco;
    • Dionisi‐Vici, Carlo
    Publication type:
    Article
    10

    Health‐related quality of life in paediatric patients with intoxication‐type inborn errors of metabolism: Analysis of an international data set.

    Published in:
    Journal of Inherited Metabolic Disease, 2021, v. 44, n. 1, p. 215, doi. 10.1002/jimd.12301
    By:
    • Bösch, Florin;
    • Landolt, Markus A.;
    • Baumgartner, Matthias R.;
    • Zeltner, Nina;
    • Kölker, Stefan;
    • Gleich, Florian;
    • Burlina, Alberto;
    • Cazzorla, Chiara;
    • Packman, Wendy;
    • V. D. Schwartz, Ida;
    • Neto, Eduardo;
    • Ribeiro, Márcia G.;
    • Martinelli, Diego;
    • Olivieri, Giorgia;
    • Huemer, Martina
    Publication type:
    Article
    11

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

    Published in:
    Journal of Inherited Metabolic Disease, 2020, v. 43, n. 6, p. 1173, doi. 10.1002/jimd.12287
    By:
    • 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
    Publication type:
    Article
    12

    Early neurodevelopmental characterization in children with cobalamin C/defect.

    Published in:
    Journal of Inherited Metabolic Disease, 2020, v. 43, n. 2, p. 367, doi. 10.1002/jimd.12171
    By:
    • Ricci, Daniela;
    • Martinelli, Diego;
    • Ferrantini, Gloria;
    • Lucibello, Simona;
    • Gambardella, MLuigia;
    • Olivieri, Giorgia;
    • Chieffo, Daniela;
    • Battaglia, Domenica;
    • Diodato, Daria;
    • Iarossi, Giancarlo;
    • Donati, Alice M.;
    • Dionisi‐Vici, Carlo;
    • Battini, Roberta;
    • Mercuri, Eugenio M.
    Publication type:
    Article
    13

    Phenotype, treatment practice and outcome in the cobalamin‐dependent remethylation disorders and MTHFR deficiency: Data from the E‐HOD registry.

    Published in:
    Journal of Inherited Metabolic Disease, 2019, v. 42, n. 2, p. 333, doi. 10.1002/jimd.12041
    By:
    • Huemer, Martina;
    • Diodato, Daria;
    • Martinelli, Diego;
    • Olivieri, Giorgia;
    • Blom, Henk;
    • Gleich, Florian;
    • Kölker, Stefan;
    • Kožich, Viktor;
    • Morris, Andrew A.;
    • Seifert, Burkhardt;
    • Froese, D. Sean;
    • Baumgartner, Matthias R.;
    • Dionisi‐Vici, Carlo;
    • Martin, Carlos Alcalde;
    • Baethmann, Martina;
    • Ballhausen, Diana;
    • Blasco‐Alonso, Javier;
    • Boy, Nikolas;
    • Bueno, Maria;
    • Burgos Peláez, Rosa
    Publication type:
    Article
    14
    15
    16
    17
    18
    19

    Donor-Acceptor Shape Matching Drives Performance in Photovoltaics.

    Published in:
    Advanced Energy Materials, 2013, v. 3, n. 7, p. 894, doi. 10.1002/aenm.201201125
    By:
    • Schiros, Theanne;
    • Kladnik, Gregor;
    • Prezzi, Deborah;
    • Ferretti, Andrea;
    • Olivieri, Giorgia;
    • Cossaro, Albano;
    • Floreano, Luca;
    • Verdini, Alberto;
    • Schenck, Christine;
    • Cox, Marshall;
    • Gorodetsky, Alon A.;
    • Plunkett, Kyle;
    • Delongchamp, Dean;
    • Nuckolls, Colin;
    • Morgante, Alberto;
    • Cvetko, Dean;
    • Kymissis, Ioannis
    Publication type:
    Article
    20
    21

    Natural history of epilepsy in argininosuccinic aciduria provides new insights into pathophysiology: A retrospective international study.

    Published in:
    Epilepsia (Series 4), 2023, v. 64, n. 6, p. 1612, doi. 10.1111/epi.17596
    By:
    • Elkhateeb, Nour;
    • Olivieri, Giorgia;
    • Siri, Barbara;
    • Boyd, Stewart;
    • Stepien, Karolina M.;
    • Sharma, Reena;
    • Morris, Andrew A. M.;
    • Hartley, Thomas;
    • Crowther, Laura;
    • Grunewald, Stephanie;
    • Cleary, Maureen;
    • Mundy, Helen;
    • Chakrapani, Anupam;
    • Lachmann, Robin;
    • Murphy, Elaine;
    • Santra, Saikat;
    • Uudelepp, Mari‐Liis;
    • Yeo, Mildrid;
    • Bernhardt, Isaac;
    • Sudakhar, Sniya
    Publication type:
    Article
    22
    23
    24
    25