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

Silvia Parisi

Showing results (41-50 of 74) with videos related to

Pageof 8
Sort By:
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 11, 2024
Analysis of CTG patterns in cases with metabolic acidosis at birth with and without neonatal neurological alterationsRossella Attini, Benedetta Montersino, Elisabetta Versino, et al.
Scientific Reports|June 24, 2020
Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
Scientific Reports|January 28, 2021
Identification of RNA-binding proteins that partner with Lin28a to regulate Dnmt3a expressionSilvia Parisi, Daniela Castaldo, Silvia Piscitelli, et al.
Scientific Reports|April 30, 2020
Bmi1 inhibitor PTC-209 promotes Chemically-induced Direct Cardiac Reprogramming of cardiac fibroblasts into cardiomyocytesGianluca Testa, Michele Russo, Giorgia Di Benedetto, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2020
Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7BMafalda Concilli, Raffaella Petruzzelli, Silvia Parisi, et al.
Scientific Reports|April 21, 2018
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 10, 2012
Pregnancy in CKD: whom should we follow and why?Giorgina Barbara Piccoli, Federica Fassio, Rossella Attini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 15, 2013
Pre-eclampsia or chronic kidney disease? The flow hypothesisGiorgina B Piccoli, Pietro Gaglioti, Rossella Attini, et al.
BMC Nephrology|March 1, 2013
Excessive urinary tract dilatation and proteinuria in pregnancy: a common and overlooked association?Giorgina B Piccoli, Rossella Attini, Silvia Parisi, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|August 11, 2024
Analysis of CTG patterns in cases with metabolic acidosis at birth with and without neonatal neurological alterationsRossella Attini, Benedetta Montersino, Elisabetta Versino, et al.
Scientific Reports|June 24, 2020
Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
Scientific Reports|January 28, 2021
Identification of RNA-binding proteins that partner with Lin28a to regulate Dnmt3a expressionSilvia Parisi, Daniela Castaldo, Silvia Piscitelli, et al.
Scientific Reports|April 30, 2020
Bmi1 inhibitor PTC-209 promotes Chemically-induced Direct Cardiac Reprogramming of cardiac fibroblasts into cardiomyocytesGianluca Testa, Michele Russo, Giorgia Di Benedetto, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2020
Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7BMafalda Concilli, Raffaella Petruzzelli, Silvia Parisi, et al.
Scientific Reports|April 21, 2018
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 10, 2012
Pregnancy in CKD: whom should we follow and why?Giorgina Barbara Piccoli, Federica Fassio, Rossella Attini, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 15, 2013
Pre-eclampsia or chronic kidney disease? The flow hypothesisGiorgina B Piccoli, Pietro Gaglioti, Rossella Attini, et al.
BMC Nephrology|March 1, 2013
Excessive urinary tract dilatation and proteinuria in pregnancy: a common and overlooked association?Giorgina B Piccoli, Rossella Attini, Silvia Parisi, et al.
Journal of the Peripheral Nervous System : JPNS|November 11, 2019
Insights into the pathogenesis of ATP1A1-related CMT disease using patient-specific iPSCsFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Pageof 8