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

Roberta Russo

Showing results (161-170 of 169) with videos related to

Pageof 17
Sort By:
You have reached the last page of results.This site can display upto 169 results.
Haematologica|May 28, 2017
Recommendations regarding splenectomy in hereditary hemolytic anemiasAchille Iolascon, Immacolata Andolfo, Wilma Barcellini, et al.
Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.
Diagnostic and Interventional Imaging|July 24, 2024
Detection and characterization of pancreatic lesion with artificial intelligence: The SFR 2023 artificial intelligence data challengeTheodore Aouad, Valerie Laurent, Paul Levant, et al.
The Journal of Clinical Investigation|April 6, 2021
The pyruvate kinase activator mitapivat reduces hemolysis and improves anemia in a β-thalassemia mouse modelAlessandro Matte, Enrica Federti, Charles Kung, et al.
Blood|March 13, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1Immacolata Andolfo, Seth L Alper, Lucia De Franceschi, et al.
EMBO Reports|May 30, 2024
Targeting ATP2B1 impairs PI3K/Akt/FOXO signaling and reduces SARS-COV-2 infection and replicationPasqualino de Antonellis, Veronica Ferrucci, Marco Miceli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2022
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individualsGiuseppe D'Alterio, Vito Alessandro Lasorsa, Ferdinando Bonfiglio, et al.
Cell Genomics|April 21, 2023
Analysis of the <i>P. lividus</i> sea urchin genome highlights contrasting trends of genomic and regulatory evolution in deuterostomesFerdinand Marlétaz, Arnaud Couloux, Julie Poulain, et al.
Orphanet Journal of Rare Diseases|April 16, 2025
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNetPablo Velasco Puyo, Soteroula Christou, Saveria Campisi, et al.
Pageof 17

Showing results (161-170 of 169) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 169 results.
Haematologica|May 28, 2017
Recommendations regarding splenectomy in hereditary hemolytic anemiasAchille Iolascon, Immacolata Andolfo, Wilma Barcellini, et al.
Nature Genetics|June 30, 2009
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type IIKlaus Schwarz, Achille Iolascon, Fatima Verissimo, et al.
Diagnostic and Interventional Imaging|July 24, 2024
Detection and characterization of pancreatic lesion with artificial intelligence: The SFR 2023 artificial intelligence data challengeTheodore Aouad, Valerie Laurent, Paul Levant, et al.
The Journal of Clinical Investigation|April 6, 2021
The pyruvate kinase activator mitapivat reduces hemolysis and improves anemia in a β-thalassemia mouse modelAlessandro Matte, Enrica Federti, Charles Kung, et al.
Blood|March 13, 2013
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1Immacolata Andolfo, Seth L Alper, Lucia De Franceschi, et al.
EMBO Reports|May 30, 2024
Targeting ATP2B1 impairs PI3K/Akt/FOXO signaling and reduces SARS-COV-2 infection and replicationPasqualino de Antonellis, Veronica Ferrucci, Marco Miceli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2022
Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individualsGiuseppe D'Alterio, Vito Alessandro Lasorsa, Ferdinando Bonfiglio, et al.
Cell Genomics|April 21, 2023
Analysis of the <i>P. lividus</i> sea urchin genome highlights contrasting trends of genomic and regulatory evolution in deuterostomesFerdinand Marlétaz, Arnaud Couloux, Julie Poulain, et al.
Orphanet Journal of Rare Diseases|April 16, 2025
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNetPablo Velasco Puyo, Soteroula Christou, Saveria Campisi, et al.
Pageof 17