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Oxidative abnormalities in Menkes disease.
Published in:
Journal of Inherited Metabolic Disease, 2000, v. 23, n. 4, p. 349, doi. 10.1023/A:1005675012708
By:
- Rizzo, C.;
- Bertini, E.;
- Piemonte, F.;
- Leuzzi, V.;
- Sabetta, G.;
- Federici, G.;
- Luchetti, A.;
- Dionisi-Vici, C.
Publication type:
Article
DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7.
Published in:
Clinical Genetics, 2017, v. 92, n. 1, p. 18, doi. 10.1111/cge.12841
By:
- Di Nottia, M.;
- Masciullo, M.;
- Verrigni, D.;
- Petrillo, S.;
- Modoni, A.;
- Rizzo, V.;
- Di Giuda, D.;
- Rizza, T.;
- Niceta, M.;
- Torraco, A.;
- Bianchi, M.;
- Santoro, M.;
- Bentivoglio, A.R.;
- Bertini, E.;
- Piemonte, F.;
- Carrozzo, R.;
- Silvestri, G.
Publication type:
Article
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defect.
Published in:
Clinical Genetics, 2017, v. 91, n. 6, p. 918, doi. 10.1111/cge.12931
By:
- Verrigni, D.;
- Diodato, D.;
- Di Nottia, M.;
- Torraco, A.;
- Bellacchio, E.;
- Rizza, T.;
- Tozzi, G.;
- Verardo, M.;
- Piemonte, F.;
- Tasca, G.;
- D'Amico, A.;
- Bertini, E.;
- Carrozzo, R.
Publication type:
Article
A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia.
Published in:
Clinical Genetics, 2017, v. 91, n. 3, p. 441, doi. 10.1111/cge.12790
By:
- Torraco, A.;
- Bianchi, M.;
- Verrigni, D.;
- Gelmetti, V.;
- Riley, L.;
- Niceta, M.;
- Martinelli, D.;
- Montanari, A.;
- Guo, Y.;
- Rizza, T.;
- Diodato, D.;
- Di Nottia, M.;
- Lucarelli, B.;
- Sorrentino, F.;
- Piemonte, F.;
- Francisci, S.;
- Tartaglia, M.;
- Valente, E.M.;
- Dionisi‐Vici, C.;
- Christodoulou, J.
Publication type:
Article
OXPHOS and mtDNA alterations in a family with spastic paraparesis.
Published in:
Acta Neurologica Scandinavica, 2000, v. 101, n. 4, p. 255, doi. 10.1034/j.1600-0404.2000.101004255.x
By:
- Santorelli, F. M.;
- Piemonte, F.;
- Carrozzo, R.;
- Tessa, A.;
- Patrono, C.;
- Tozzi, G.;
- Bertini, E.
Publication type:
Article
Glutathione in blood of patients with Friedreich's ataxia.
Published in:
European Journal of Clinical Investigation, 2001, v. 31, n. 11, p. 1007, doi. 10.1046/j.1365-2362.2001.00922.x
By:
- Piemonte, F.;
- Pastore, A.;
- Tozzi, G.;
- Tagliacozzi, D.;
- Santorelli, F. M.;
- Carrozzo, R.;
- Casali, C.;
- Damiano, M.;
- Federici, G.;
- Bertini, E.
Publication type:
Article
Endotoxin and plasminogen activator inhibitor-1 serum levels associated with nonalcoholic steatohepatitis in children.
Published in:
2010
By:
- Alisi A;
- Manco M;
- Devito R;
- Piemonte F;
- Nobili V
Publication type:
Journal Article
NAFLD IN CHILDREN: A SINGLE‐CENTER EXPERIENCE.
Published in:
Journal of Pediatric Gastroenterology & Nutrition, 2006, v. 42, n. 5, p. E61-E62, doi. 10.1002/j.1536-4801.2006.tb01933.x
By:
- Nobili, V;
- Marcellini, M;
- Devito, R;
- Ciampalini, P;
- Comparcola, D;
- Sartorelli, MR;
- Piemonte, F;
- Angulo, P
Publication type:
Article
O0114 GLUTATHIONE BLOOD PROFILE IN CHILDREN AFFECTED BY NASH.
Published in:
Journal of Pediatric Gastroenterology & Nutrition, 2004, v. 39, p. S52, doi. 10.1097/00005176-200406001-00116
By:
- Nobili, V.;
- Pastore, A.;
- Gaeta, L.;
- Tozzi, G.;
- Comparcola, D.;
- Sartorelli, M.;
- Marcellini, M.;
- Bertini, E.;
- Piemonte, F.
Publication type:
Article
Effect of vitamin E on aminotransferase levels and insulin resistance in children with non-alcoholic fatty liver disease.
Published in:
Alimentary Pharmacology & Therapeutics, 2006, v. 24, n. 11/12, p. 1553, doi. 10.1111/j.1365-2036.2006.03161.x
By:
- NOBILI, V.;
- MANCO, M.;
- DEVITO, R.;
- CIAMPALINI, P.;
- PIEMONTE, F.;
- MARCELLINI, M.
Publication type:
Article

Found: 10