Fiorella Piemonte - Concepedia

Author

Fiorella Piemonte

Also Known As

E. Guerri, F Gatto, F Piemonte, F. PIEMONTE, F. Piemonte, FIORELLA PIEMONTE, Fiorella PIEMONTE, Fiorella Piemonte, Piemonte, F, Piemonte, Fiorella

178

Publications

9.1K

Citations

H-Index

167

Concepts

All Affiliations

Bambino Gesù Children's Hospital Istituti di Ricovero e Cura a Carattere Scientifico Sapienza University of Rome University of Rome Tor Vergata Boston Children's Hospital

About

Fiorella Piemonte is an author at Bambino Gesù Children's Hospital specializing in medicine, biochemistry, and oxidative stress.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	35	62	4K
2	Health Sciences	13	13	943
3	Natural Sciences	6	6	537
4	Social Sciences	6	6	550
5	Engineering	1	1	42

Fiorella Piemonte

101

Publications

7.1K

Citations

H-Index

Page 1

	Year	Citations
Lifestyle intervention and antioxidant therapy in children with nonalcoholic fatty liver disease Valério Nobili, Melania Manco, Rita De Vito, Hepatology	2008	406
NAFLD in children: A prospective clinical-pathological study and effect of lifestyle advice Valério Nobili, Matilde Marcellini, Rita De Vito, Hepatology NutritionMetabolic DisorderPediatric NafldFatty Liver DiseaseLifestyle Advice	2006	351
COQ2 Nephropathy Francesca Diomedi‐Camassei, Silvia Di Giandomenico, Filippo M. Santorelli, Journal of the American Society of Nephrology Glomerular DiseaseGlomerulonephritisUrologyRenal DiseaseRenal Function	2007	326
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport Fátima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Journal of Clinical Investigation	2004	269
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport Fátima Ferreirinha, Angelo Quattrini, Marinella Pirozzi, Journal of Clinical Investigation GeneticsCell DeathPeripheral NervesSynaptic SignalingCellular Physiology	2004	268
Determination of Blood Total, Reduced, and Oxidized Glutathione in Pediatric Subjects Anna Pastore, Fiorella Piemonte, Mattia Locatelli, Clinical Chemistry	2001	213
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness Rosalba Carrozzo, Carlo Dionisi‐Vici, Ulrike Steuerwald, Brain GeneticsPathologyMolecular BiologyMolecular GeneticsDisease Gene Identification	2007	204
Mirnome analysis reveals novel molecular determinants in the pathogenesis of diet-induced nonalcoholic fatty liver disease Anna Alisi, Letizia Da Sacco, G. Bruscalupi, Laboratory Investigation Mirnome Analysis RevealsMetabolic SyndromeSystems BiologyMetabolic Associated SteatohepatitisHepatology	2010	194
EPI-743 reverses the progression of the pediatric mitochondrial disease—Genetically defined Leigh Syndrome Diego Martinelli, Michela Catteruccia, Fiorella Piemonte, Molecular Genetics and Metabolism Mitochondrial FunctionGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2012	184
Effect of vitamin E on aminotransferase levels and insulin resistance in children with non‐alcoholic fatty liver disease Valério Nobili, Melania Manco, Paolo Ciampalini, Alimentary Pharmacology & Therapeutics	2006	180

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