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Federica Invernizzi

Showing results (61-70 of 115) with videos related to

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Nature Genetics|May 26, 2009
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathyDaniele Ghezzi, Paola Goffrini, Graziella Uziel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 25, 2016
DYT2 screening in early-onset isolated dystoniaMiryam Carecchio, Chiara Reale, Federica Invernizzi, et al.
Parkinsonism & Related Disorders|April 2, 2025
Myoclonic manifestations and skin inclusions as diagnostic clues in ATP13A2-related disordersChiara Benzoni, Gianluca Marucci, Chiara Pisciotta, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|November 20, 2016
Prevention of hepatitis C recurrence by bridging sofosbuvir/ribavirin from pre- to post-liver transplant: a real-life strategyMaria Francesca Donato, Cristina Morelli, Renato Romagnoli, et al.
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|March 17, 2021
Cost analysis of a long-term randomized controlled study in biliary duct-to-duct anastomotic stricture after liver transplantationPaolo Cantù, Giulio Santi, Roberto Rosa, et al.
Neurology|June 28, 2015
Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutationsLaura Canafoglia, Isabella Gilioli, Federica Invernizzi, et al.
Brain : a Journal of Neurology|May 31, 2007
Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathyEdoardo Malfatti, Marianna Bugiani, Federica Invernizzi, et al.
Human Mutation|September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiencyVito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|September 16, 2019
High prevalence of early atherosclerotic and cardiac damage in patients undergoing liver transplantation: Preliminary resultsGiuseppina Pisano, Maria Francesca Donato, Dario Consonni, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Nature Genetics|May 26, 2009
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathyDaniele Ghezzi, Paola Goffrini, Graziella Uziel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 25, 2016
DYT2 screening in early-onset isolated dystoniaMiryam Carecchio, Chiara Reale, Federica Invernizzi, et al.
Parkinsonism & Related Disorders|April 2, 2025
Myoclonic manifestations and skin inclusions as diagnostic clues in ATP13A2-related disordersChiara Benzoni, Gianluca Marucci, Chiara Pisciotta, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|November 20, 2016
Prevention of hepatitis C recurrence by bridging sofosbuvir/ribavirin from pre- to post-liver transplant: a real-life strategyMaria Francesca Donato, Cristina Morelli, Renato Romagnoli, et al.
American Journal of Human Genetics|May 22, 2012
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosisDaniele Ghezzi, Enrico Baruffini, Tobias B Haack, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|March 17, 2021
Cost analysis of a long-term randomized controlled study in biliary duct-to-duct anastomotic stricture after liver transplantationPaolo Cantù, Giulio Santi, Roberto Rosa, et al.
Neurology|June 28, 2015
Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutationsLaura Canafoglia, Isabella Gilioli, Federica Invernizzi, et al.
Brain : a Journal of Neurology|May 31, 2007
Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathyEdoardo Malfatti, Marianna Bugiani, Federica Invernizzi, et al.
Human Mutation|September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiencyVito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|September 16, 2019
High prevalence of early atherosclerotic and cardiac damage in patients undergoing liver transplantation: Preliminary resultsGiuseppina Pisano, Maria Francesca Donato, Dario Consonni, et al.
Pageof 12