Vito Porcelli - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Vito Porcelli

Showing results (31-40 of 36) with videos related to

Pageof 4

Sort By:

You have reached the last page of results.This site can display upto 36 results.

Human Molecular Genetics|December 7, 2017

SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiencyGiuseppe Punzi, Vito Porcelli, Matteo Ruggiu, et al.

Journal of Neuromuscular Diseases|February 13, 2016

Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular TransmissionAmina Chaouch, Vito Porcelli, Daniel Cox, et al.

Journal of Proteome Research|August 23, 2017

Toward the Standardization of Mitochondrial Proteomics: The Italian Mitochondrial Human Proteome Project InitiativeTiziana Alberio, Luisa Pieroni, Maurizio Ronci, et al.

Journal of Inherited Metabolic Disease|December 15, 2017

An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variantsAna Pop, Monique Williams, Eduard A Struys, et al.

Cell Death & Disease|December 15, 2025

Combined ketone body and glutamine supplementation restores aerobic energy production in AGC1-deficient neuronal progenitorsSimona Nicole Barile, Maria Chiara Magnifico, Eleonora Poeta, et al.

Nutrients|September 9, 2022

Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate CarrierBigna K Bölsterli, Eugen Boltshauser, Luigi Palmieri, et al.

Pageof 4

Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

Human Molecular Genetics|December 7, 2017

SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiencyGiuseppe Punzi, Vito Porcelli, Matteo Ruggiu, et al.

Journal of Neuromuscular Diseases|February 13, 2016

Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular TransmissionAmina Chaouch, Vito Porcelli, Daniel Cox, et al.

Journal of Proteome Research|August 23, 2017

Toward the Standardization of Mitochondrial Proteomics: The Italian Mitochondrial Human Proteome Project InitiativeTiziana Alberio, Luisa Pieroni, Maurizio Ronci, et al.

Journal of Inherited Metabolic Disease|December 15, 2017

An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variantsAna Pop, Monique Williams, Eduard A Struys, et al.

Cell Death & Disease|December 15, 2025

Combined ketone body and glutamine supplementation restores aerobic energy production in AGC1-deficient neuronal progenitorsSimona Nicole Barile, Maria Chiara Magnifico, Eleonora Poeta, et al.

Nutrients|September 9, 2022

Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate CarrierBigna K Bölsterli, Eugen Boltshauser, Luigi Palmieri, et al.

Pageof 4