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

Sara Vila-Bedmar

Showing results (1-10 of 3) with videos related to

Pageof 1
Sort By:
Indian Journal of Pediatrics|April 25, 2022
Rituximab as Second-Line Treatment in Anti-NMDAR Encephalitis after Herpes Simplex Encephalitis in ChildrenPaula Carrascosa-García, Lidia Oviedo-Melgares, David Torres-Fernández, et al.
The Pediatric Infectious Disease Journal|June 14, 2025
Brain Abnormalities, Neurodevelopmental Milestones, and Long-term Follow-up in Newborns With Congenital Cytomegalovirus Identified Through a Neonatal Screening ProgramSara Vila-Bedmar, Ana Martinez de Aragon Calvo, Constanza Liebana-Rojas, et al.
Journal of Medical Genetics|May 17, 2023
Expanding the phenotypic spectrum of <i>TRAPPC11-</i>related muscular dystrophy: 25 Roma individuals carrying a founder variantMaria Justel, Cristina Jou, Andrea Sariego-Jamardo, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Indian Journal of Pediatrics|April 25, 2022
Rituximab as Second-Line Treatment in Anti-NMDAR Encephalitis after Herpes Simplex Encephalitis in ChildrenPaula Carrascosa-García, Lidia Oviedo-Melgares, David Torres-Fernández, et al.
The Pediatric Infectious Disease Journal|June 14, 2025
Brain Abnormalities, Neurodevelopmental Milestones, and Long-term Follow-up in Newborns With Congenital Cytomegalovirus Identified Through a Neonatal Screening ProgramSara Vila-Bedmar, Ana Martinez de Aragon Calvo, Constanza Liebana-Rojas, et al.
Journal of Medical Genetics|May 17, 2023
Expanding the phenotypic spectrum of <i>TRAPPC11-</i>related muscular dystrophy: 25 Roma individuals carrying a founder variantMaria Justel, Cristina Jou, Andrea Sariego-Jamardo, et al.
Pageof 1