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

Federica Invernizzi

Showing results (21-30 of 115) with videos related to

Pageof 12
Sort By:
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Neurology|July 28, 2017
Thiamine-responsive disease due to mutation of <i>tpk1</i>: Importance of avoiding misdiagnosisFederica Invernizzi, Celeste Panteghini, Luisa Chiapparini, et al.
Parkinsonism & Related Disorders|November 10, 2023
Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen yearsCeleste Panteghini, Chiara Reale, Isabel Colangelo, et al.
United European Gastroenterology Journal|August 21, 2019
Safety of vedolizumab in liver transplant recipients: A systematic reviewMarco Spadaccini, Alessio Aghemo, Flavio Caprioli, et al.
European Journal of Medical Genetics|April 6, 2018
Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?Federica Invernizzi, Giovanna Zorzi, Andrea Legati, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Neuromuscular Disorders : NMD|May 28, 2008
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathyGiuliana Galassi, Eleonora Lamantea, Federica Invernizzi, et al.
Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 27, 2025
Sex differences in hepatic encephalopathy: addressing the knowledge gapLucia Lapenna, Manuela Merli, Marta Cilla, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 14, 2011
Long-term add-on therapy with adefovir in lamivudine-resistant kidney graft recipients with chronic hepatitis BPietro Lampertico, Mauro ViganĂ², Floriana Facchetti, et al.
Pageof 12

Showing results (21-30 of 115) with videos related to

Sort By:
Pageof 12
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Neurology|July 28, 2017
Thiamine-responsive disease due to mutation of <i>tpk1</i>: Importance of avoiding misdiagnosisFederica Invernizzi, Celeste Panteghini, Luisa Chiapparini, et al.
Parkinsonism & Related Disorders|November 10, 2023
Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen yearsCeleste Panteghini, Chiara Reale, Isabel Colangelo, et al.
United European Gastroenterology Journal|August 21, 2019
Safety of vedolizumab in liver transplant recipients: A systematic reviewMarco Spadaccini, Alessio Aghemo, Flavio Caprioli, et al.
European Journal of Medical Genetics|April 6, 2018
Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?Federica Invernizzi, Giovanna Zorzi, Andrea Legati, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Neuromuscular Disorders : NMD|May 28, 2008
Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathyGiuliana Galassi, Eleonora Lamantea, Federica Invernizzi, et al.
Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|April 27, 2025
Sex differences in hepatic encephalopathy: addressing the knowledge gapLucia Lapenna, Manuela Merli, Marta Cilla, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 14, 2011
Long-term add-on therapy with adefovir in lamivudine-resistant kidney graft recipients with chronic hepatitis BPietro Lampertico, Mauro ViganĂ², Floriana Facchetti, et al.
Pageof 12