Ivano Di Meo - Concepedia

Author

Ivano Di Meo

Fondazione IRCCS Istituto Neurologico Carlo Besta ORCID

Also Known As

DI MEO, Ivano, Di Meo, Ivano, I Di Meo, I DiMeo, I. Di Meo, Ivano Di Meo

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Fondazione IRCCS Istituto Neurologico Carlo Besta Istituti di Ricovero e Cura a Carattere Scientifico Vita-Salute San Raffaele University MRC Mitochondrial Biology Unit Telethon Institute Of Genetics And Medicine

About

Ivano Di Meo is an author at Fondazione IRCCS Istituto Neurologico Carlo Besta specializing in medicine, mitochondrial function, and oxidative stress.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	774
2	Health Sciences	2	2	152
3	Engineering	1	1	30
4	Natural Sciences	1	1	36
5	Public Health	1	1	37

Ivano Di Meo

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy Valeria Tiranti, Carlo Viscomi, Tatjana M. Hildebrandt, Nature Medicine Mitochondrial DioxygenaseBiochemistryMitochondrial FunctionEthylmalonic EncephalopathyMedicine	2009	400
Transcription Factor EB Controls Metabolic Flexibility during Exercise Gelsomina Mansueto, Andrea Armani, Carlo Viscomi, Cell Metabolism	2016	318
Dissection of metabolic reprogramming in polycystic kidney disease reveals coordinated rewiring of bioenergetic pathways Christine Podrini, Isaline Rowe, Roberto Pagliarini, Communications Biology	2018	97
Chronic Exposure to Sulfide Causes Accelerated Degradation of Cytochrome c Oxidase in Ethylmalonic Encephalopathy Ivano Di Meo, Gigliola Fagiolari, A. Prelle, Antioxidants and Redox Signaling Ethylmalonic EncephalopathyLipid PeroxidationCell DeathPathologyRedox Biology	2010	94
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder Valentina Del Dotto, Farid Ullah, Ivano Di Meo, Journal of Clinical Investigation Mtdna DepletionMitochondrial DysfunctionGeneticsMolecular BiologyMolecular Genetics	2019	91
Effective AAV‐mediated gene therapy in a mouse model of ethylmalonic encephalopathy Ivano Di Meo, Alberto Auricchio, Costanza Lamperti, EMBO Molecular Medicine	2012	85
Coenzyme Q deficiency causes impairment of the sulfide oxidation pathway Marcello Ziosi, Ivano Di Meo, Giulio Kleiner, EMBO Molecular Medicine	2016	74
Liver transplant in ethylmalonic encephalopathy: a new treatment for an otherwise fatal disease Carlo Dionisi‐Vici, Daria Diodato, Giuliano Torre, Brain	2016	69
Identification of new mutations in the <i>ETHE1</i> gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy Rossana Mineri, M. Rimoldi, Alberto Burlina, Journal of Medical Genetics	2008	66
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome Ivano Di Meo, Silvia Marchet, Costanza Lamperti, Gene Therapy	2017	64

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