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Federica Invernizzi

Showing results (71-80 of 115) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2021
YY1-Related Dystonia: Clinical Aspects and Long-Term Response to Deep Brain StimulationGiovanna Zorzi, Ignacio Juan Keller Sarmiento, Federica Rachele Danti, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|August 20, 2024
Sex disparities in acute-on-chronic liver failure: From admission to the intensive care unit to liver transplantationElisabetta Cerutti, Francesca D'Arcangelo, Chiara Becchetti, et al.
Hepatology (Baltimore, Md.)|September 12, 2015
Natural killer cell phenotype modulation and natural killer/T-cell interplay in nucleos(t)ide analogue-treated hepatitis e antigen-negative patients with chronic hepatitis BCarolina Boni, Pietro Lampertico, Lavinia Talamona, et al.
Transplantation|September 14, 2019
Experience With Early Sorafenib Treatment With mTOR Inhibitors in Hepatocellular Carcinoma Recurring After Liver TransplantationFederica Invernizzi, Massimo Iavarone, Claudio Zavaglia, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
A novel AIFM1 mutation expands the phenotype to an infantile motor neuron diseaseDaria Diodato, Giorgio Tasca, Daniela Verrigni, et al.
Movement Disorders Clinical Practice|November 29, 2023
Unraveling Autonomic Dysfunction in GBA-Related Parkinson's DiseaseGrazia Devigili, Giulia Straccia, Emanuele Cereda, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Parkinsonism & Related Disorders|March 20, 2022
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonismBarbara Garavaglia, Sadeq Vallian, Luigi M Romito, et al.
JIMD Reports|April 18, 2014
Common and Novel TMEM70 Mutations in a Cohort of Italian Patients with Mitochondrial EncephalocardiomyopathyDaria Diodato, Federica Invernizzi, Eleonora Lamantea, et al.
The Lancet. Gastroenterology & Hepatology|June 8, 2020
COVID-19 in liver transplant recipients: preliminary data from the ELITA/ELTR registryLuca S Belli, Christophe Duvoux, Vincent Karam, et al.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2021
YY1-Related Dystonia: Clinical Aspects and Long-Term Response to Deep Brain StimulationGiovanna Zorzi, Ignacio Juan Keller Sarmiento, Federica Rachele Danti, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|August 20, 2024
Sex disparities in acute-on-chronic liver failure: From admission to the intensive care unit to liver transplantationElisabetta Cerutti, Francesca D'Arcangelo, Chiara Becchetti, et al.
Hepatology (Baltimore, Md.)|September 12, 2015
Natural killer cell phenotype modulation and natural killer/T-cell interplay in nucleos(t)ide analogue-treated hepatitis e antigen-negative patients with chronic hepatitis BCarolina Boni, Pietro Lampertico, Lavinia Talamona, et al.
Transplantation|September 14, 2019
Experience With Early Sorafenib Treatment With mTOR Inhibitors in Hepatocellular Carcinoma Recurring After Liver TransplantationFederica Invernizzi, Massimo Iavarone, Claudio Zavaglia, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
A novel AIFM1 mutation expands the phenotype to an infantile motor neuron diseaseDaria Diodato, Giorgio Tasca, Daniela Verrigni, et al.
Movement Disorders Clinical Practice|November 29, 2023
Unraveling Autonomic Dysfunction in GBA-Related Parkinson's DiseaseGrazia Devigili, Giulia Straccia, Emanuele Cereda, et al.
Epilepsia Open|December 24, 2024
CLN6-related continuum phenotype caused by aberrant splicingFederica Invernizzi, Barbara Castellotti, Chiara Reale, et al.
Parkinsonism & Related Disorders|March 20, 2022
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonismBarbara Garavaglia, Sadeq Vallian, Luigi M Romito, et al.
JIMD Reports|April 18, 2014
Common and Novel TMEM70 Mutations in a Cohort of Italian Patients with Mitochondrial EncephalocardiomyopathyDaria Diodato, Federica Invernizzi, Eleonora Lamantea, et al.
The Lancet. Gastroenterology & Hepatology|June 8, 2020
COVID-19 in liver transplant recipients: preliminary data from the ELITA/ELTR registryLuca S Belli, Christophe Duvoux, Vincent Karam, et al.
Pageof 12