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

Vitorina Passão

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

Pageof 1
Sort By:
Epilepsy & Behavior : E&B|December 31, 2003
Comparison between the results of the Symptom Checklist-90 in two different populations with temporal lobe epilepsyInês Cunha, Sofia Brissos, Marina Dinis, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 5, 2002
Interictal spike EEG source analysis in hypothalamic hamartoma epilepsyAlberto J R Leal, Vitorina Passão, Eulália Calado, et al.
Journal of Human Genetics|July 22, 2006
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotypeMaria do Carmo Costa, Andreia Teixeira-Castro, Marco Constante, et al.
Pageof 1

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

Sort By:
Pageof 1
Epilepsy & Behavior : E&B|December 31, 2003
Comparison between the results of the Symptom Checklist-90 in two different populations with temporal lobe epilepsyInês Cunha, Sofia Brissos, Marina Dinis, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 5, 2002
Interictal spike EEG source analysis in hypothalamic hamartoma epilepsyAlberto J R Leal, Vitorina Passão, Eulália Calado, et al.
Journal of Human Genetics|July 22, 2006
Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotypeMaria do Carmo Costa, Andreia Teixeira-Castro, Marco Constante, et al.
Pageof 1