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

Andreina Bordoni

Showing results (1-10 of 54) with videos related to

Pageof 6
Sort By:
Critical Care Medicine|December 15, 2015
Changes in Whole-Body Oxygen Consumption and Skeletal Muscle Mitochondria During Linezolid-Induced Lactic AcidosisAlessandro Protti, Dario Ronchi, Gabriele Bassi, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletionMarco Crimi, Roberto Del Bo, Sara Galbiati, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 8, 2006
A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeastManuela Sironi, Uberto Pozzoli, Giacomo P Comi, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Mitochondrion|August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new casesMarco Crimi, Sara Galbiati, Monica Sciacco, et al.
Journal of the Neurological Sciences|September 11, 2002
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patientsRoberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, et al.
Human Mutation|October 29, 2002
A collection of 33 novel human mtDNA homoplasmic variantsMarco Crimi, Monica Sciacco, Sara Galbiati, et al.
Respiratory Physiology & Neurobiology|March 19, 2013
Postural effects on lung and chest wall volumes in late onset type II glycogenosis patientsGauthier Remiche, Antonella Lo Mauro, Paolo Tarsia, et al.
Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Critical Care Medicine|December 15, 2015
Changes in Whole-Body Oxygen Consumption and Skeletal Muscle Mitochondria During Linezolid-Induced Lactic AcidosisAlessandro Protti, Dario Ronchi, Gabriele Bassi, et al.
European Journal of Human Genetics : EJHG|October 23, 2003
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletionMarco Crimi, Roberto Del Bo, Sara Galbiati, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 8, 2006
A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeastManuela Sironi, Uberto Pozzoli, Giacomo P Comi, et al.
Human Mutation|November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletionsAlessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Journal of Neurology|October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literatureGauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Mitochondrion|August 27, 2005
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new casesMarco Crimi, Sara Galbiati, Monica Sciacco, et al.
Journal of the Neurological Sciences|September 11, 2002
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patientsRoberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, et al.
Human Mutation|October 29, 2002
A collection of 33 novel human mtDNA homoplasmic variantsMarco Crimi, Monica Sciacco, Sara Galbiati, et al.
Respiratory Physiology & Neurobiology|March 19, 2013
Postural effects on lung and chest wall volumes in late onset type II glycogenosis patientsGauthier Remiche, Antonella Lo Mauro, Paolo Tarsia, et al.
Neuromuscular Disorders : NMD|July 27, 2007
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiencyOlimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, et al.
Pageof 6