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Movement Disorders Clinical Practice
|
May 19, 2023
Two Cases of <i>TMEM151A</i>-Associated Paroxysmal Dyskinesia in a Single-Center Series of PRRT2-Negative Patients
Sara Satolli, Federica Invernizzi, Federica Rachele Danti, et al.
Human Mutation
|
September 10, 2013
A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, and severe reduction of mitochondrial complex III activity
Federica Invernizzi, Marco Tigano, Cristina Dallabona, et al.
Frontiers in Aging Neuroscience
|
October 27, 2025
Metabolic Parkinson's disease
Federica Invernizzi, Lorenzo Ciocca, Elena Contaldi, et al.
Expert Review of Clinical Immunology
|
April 22, 2026
Inflammatory bowel disease and Primary sclerosing cholangitis: immunological links and clinical outlook
Sara Massironi, Fabrizio Fanizzi, Federica Invernizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2021
THAP1 Dystonia with Globus Pallidus T2 Hypointensity: A Report of Two Cases
Giovanna Zorzi, Federica R Danti, Chiara Reale, et al.
Journal of Clinical Medicine
|
February 13, 2026
Insulin Resistance and Metabolic Dysfunction in Early-Stage Parkinson's Disease: Evidence from a Preliminary Case-Control Study
Elena Contaldi, Lorenzo Ciocca, Francesco Mignone, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
September 16, 2020
Coronavirus disease 2019 and transplantation: tackling the challenges of SARS-CoV-2 infection in waiting list candidates
Davide Mangioni, Daniele Dondossola, Barbara Antonelli, et al.
Mitochondrion
|
October 2, 2010
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
Enrico Baruffini, Rita Horvath, Cristina Dallabona, et al.
American Journal of Human Genetics
|
April 6, 2010
Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor
Daniele Ghezzi, Irina Sevrioukova, Federica Invernizzi, et al.
Journal of Personalized Medicine
|
June 24, 2022
Gender and Autoimmune Liver Diseases: Relevant Aspects in Clinical Practice
Federica Invernizzi, Marta Cilla, Silvia Trapani, et al.
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of 12
Search research articles
Search
Showing results (31-40 of 115) with videos related to
Sort By:
Page
of 12
Movement Disorders Clinical Practice
|
May 19, 2023
Two Cases of <i>TMEM151A</i>-Associated Paroxysmal Dyskinesia in a Single-Center Series of PRRT2-Negative Patients
Sara Satolli, Federica Invernizzi, Federica Rachele Danti, et al.
Human Mutation
|
September 10, 2013
A homozygous mutation in LYRM7/MZM1L associated with early onset encephalopathy, lactic acidosis, and severe reduction of mitochondrial complex III activity
Federica Invernizzi, Marco Tigano, Cristina Dallabona, et al.
Frontiers in Aging Neuroscience
|
October 27, 2025
Metabolic Parkinson's disease
Federica Invernizzi, Lorenzo Ciocca, Elena Contaldi, et al.
Expert Review of Clinical Immunology
|
April 22, 2026
Inflammatory bowel disease and Primary sclerosing cholangitis: immunological links and clinical outlook
Sara Massironi, Fabrizio Fanizzi, Federica Invernizzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 5, 2021
THAP1 Dystonia with Globus Pallidus T2 Hypointensity: A Report of Two Cases
Giovanna Zorzi, Federica R Danti, Chiara Reale, et al.
Journal of Clinical Medicine
|
February 13, 2026
Insulin Resistance and Metabolic Dysfunction in Early-Stage Parkinson's Disease: Evidence from a Preliminary Case-Control Study
Elena Contaldi, Lorenzo Ciocca, Francesco Mignone, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation
|
September 16, 2020
Coronavirus disease 2019 and transplantation: tackling the challenges of SARS-CoV-2 infection in waiting list candidates
Davide Mangioni, Daniele Dondossola, Barbara Antonelli, et al.
Mitochondrion
|
October 2, 2010
Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model
Enrico Baruffini, Rita Horvath, Cristina Dallabona, et al.
American Journal of Human Genetics
|
April 6, 2010
Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor
Daniele Ghezzi, Irina Sevrioukova, Federica Invernizzi, et al.
Journal of Personalized Medicine
|
June 24, 2022
Gender and Autoimmune Liver Diseases: Relevant Aspects in Clinical Practice
Federica Invernizzi, Marta Cilla, Silvia Trapani, et al.
Page
of 12