Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Alessandra Maresca

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
Gastroenterology|August 22, 2024
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-ObstructionChiara Diquigiovanni, Nicola Rizzardi, Erica Cataldi-Stagetti, et al.
Frontiers in Genetics|November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorderLeonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Brain : a Journal of Neurology|December 15, 2015
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversionValerio Carelli, Pio d'Adamo, Maria Lucia Valentino, et al.
Annals of Neurology|July 17, 2016
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathyRoberto De Giorgio, Loris Pironi, Rita Rinaldi, et al.
Biochimica Et Biophysica Acta|December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesionsLeonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Scientific Reports|March 18, 2020
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram SyndromeChiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Human Mutation|May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intoleranceValeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Scientific Reports|June 25, 2020
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram SyndromeChiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Plos Genetics|February 15, 2018
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathyLeonardo Caporali, Luisa Iommarini, Chiara La Morgia, et al.
Annals of Neurology|March 31, 2015
Syndromic parkinsonism and dementia associated with OPA1 missense mutationsValerio Carelli, Olimpia Musumeci, Leonardo Caporali, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Gastroenterology|August 22, 2024
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-ObstructionChiara Diquigiovanni, Nicola Rizzardi, Erica Cataldi-Stagetti, et al.
Frontiers in Genetics|November 24, 2022
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorderLeonardo Caporali, Claudio Fiorini, Flavia Palombo, et al.
Brain : a Journal of Neurology|December 15, 2015
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversionValerio Carelli, Pio d'Adamo, Maria Lucia Valentino, et al.
Annals of Neurology|July 17, 2016
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathyRoberto De Giorgio, Loris Pironi, Rita Rinaldi, et al.
Biochimica Et Biophysica Acta|December 19, 2012
Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesionsLeonardo Caporali, Anna Maria Ghelli, Luisa Iommarini, et al.
Scientific Reports|March 18, 2020
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram SyndromeChiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Human Mutation|May 28, 2014
A novel in-frame 18-bp microdeletion in MT-CYB causes a multisystem disorder with prominent exercise intoleranceValeria Carossa, Anna Ghelli, Concetta Valentina Tropeano, et al.
Scientific Reports|June 25, 2020
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram SyndromeChiara La Morgia, Alessandra Maresca, Giulia Amore, et al.
Plos Genetics|February 15, 2018
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathyLeonardo Caporali, Luisa Iommarini, Chiara La Morgia, et al.
Annals of Neurology|March 31, 2015
Syndromic parkinsonism and dementia associated with OPA1 missense mutationsValerio Carelli, Olimpia Musumeci, Leonardo Caporali, et al.
Pageof 7