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Federica Invernizzi

Showing results (41-50 of 115) with videos related to

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Hepatology (Baltimore, Md.)|April 5, 2012
IL28B polymorphisms predict interferon-related hepatitis B surface antigen seroclearance in genotype D hepatitis B e antigen-negative patients with chronic hepatitis BPietro Lampertico, Mauro Viganò, Cristina Cheroni, et al.
United European Gastroenterology Journal|March 3, 2023
Influence of sex in alcohol-related liver disease: Pre-clinical and clinical settingsDebora Bizzaro, Chiara Becchetti, Silvia Trapani, et al.
Human Molecular Genetics|February 5, 2003
Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in miceAlessandro Agostino, Federica Invernizzi, Cecilia Tiveron, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2017
SLC19A3 related disorder: Treatment implication and clinical outcome of 2 new patientsDavide Tonduti, Federica Invernizzi, Celeste Panteghini, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiencyPaola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, et al.
Brain : a Journal of Neurology|June 24, 2021
Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3Federica Invernizzi, Andrea Legati, Alessia Nasca, et al.
Molecular Genetics and Metabolism|September 27, 2012
A novel homozygous mutation in SUCLA2 gene identified by exome sequencingCostanza Lamperti, Mingyan Fang, Federica Invernizzi, et al.
Clinical Transplantation|April 3, 2020
Efficacy and safety of device-assisted enteroscopy ERCP in liver transplantation: A systematic review and meta-analysisFrancesca Ferretti, Mirella Fraquelli, Paolo Cantù, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 18, 2021
Sarcopenia in chronic advanced liver diseases: A sex-oriented analysis of the literatureMaria Guarino, Valentina Cossiga, Chiara Becchetti, et al.
Viral Immunology|July 12, 2021
The CCR5 and CXCR3 Pathways in Hepatitis C Virus Liver Transplanted Recipients Treated by a Direct Antiviral Agent Regimen: Informative Kinetics ProfilesGiuseppe Colucci, Federica Invernizzi, Sara Uceda Renteria, et al.
Pageof 12

Showing results (41-50 of 115) with videos related to

Sort By:
Pageof 12
Hepatology (Baltimore, Md.)|April 5, 2012
IL28B polymorphisms predict interferon-related hepatitis B surface antigen seroclearance in genotype D hepatitis B e antigen-negative patients with chronic hepatitis BPietro Lampertico, Mauro Viganò, Cristina Cheroni, et al.
United European Gastroenterology Journal|March 3, 2023
Influence of sex in alcohol-related liver disease: Pre-clinical and clinical settingsDebora Bizzaro, Chiara Becchetti, Silvia Trapani, et al.
Human Molecular Genetics|February 5, 2003
Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in miceAlessandro Agostino, Federica Invernizzi, Cecilia Tiveron, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2017
SLC19A3 related disorder: Treatment implication and clinical outcome of 2 new patientsDavide Tonduti, Federica Invernizzi, Celeste Panteghini, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
A novel mutation in the mitochondrial tRNA(Pro) gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiencyPaola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, et al.
Brain : a Journal of Neurology|June 24, 2021
Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3Federica Invernizzi, Andrea Legati, Alessia Nasca, et al.
Molecular Genetics and Metabolism|September 27, 2012
A novel homozygous mutation in SUCLA2 gene identified by exome sequencingCostanza Lamperti, Mingyan Fang, Federica Invernizzi, et al.
Clinical Transplantation|April 3, 2020
Efficacy and safety of device-assisted enteroscopy ERCP in liver transplantation: A systematic review and meta-analysisFrancesca Ferretti, Mirella Fraquelli, Paolo Cantù, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|November 18, 2021
Sarcopenia in chronic advanced liver diseases: A sex-oriented analysis of the literatureMaria Guarino, Valentina Cossiga, Chiara Becchetti, et al.
Viral Immunology|July 12, 2021
The CCR5 and CXCR3 Pathways in Hepatitis C Virus Liver Transplanted Recipients Treated by a Direct Antiviral Agent Regimen: Informative Kinetics ProfilesGiuseppe Colucci, Federica Invernizzi, Sara Uceda Renteria, et al.
Pageof 12