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 Chiari

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
American Journal of Medical Genetics. Part A|April 26, 2017
Lissencephaly: Expanded imaging and clinical classificationNataliya Di Donato, Sara Chiari, Ghayda M Mirzaa, et al.
Eating and Weight Disorders : EWD|March 18, 2025
Child eating disorder examination (ChEDE) interview and child eating disorder examination questionnaire (ChEDE-Q): psychometric properties of the Italian versionsLucilla Bonvini, Silvia Taddei, Saverio Caini, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2018
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephalyNataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|April 26, 2017
Lissencephaly: Expanded imaging and clinical classificationNataliya Di Donato, Sara Chiari, Ghayda M Mirzaa, et al.
Eating and Weight Disorders : EWD|March 18, 2025
Child eating disorder examination (ChEDE) interview and child eating disorder examination questionnaire (ChEDE-Q): psychometric properties of the Italian versionsLucilla Bonvini, Silvia Taddei, Saverio Caini, et al.
Neurology|February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutationsValentina Cetica, Sara Chiari, Davide Mei, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 20, 2018
Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephalyNataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, et al.
Pageof 1