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

Maria A Pastor

Showing results (31-40 of 44) with videos related to

Pageof 5
Sort By:
Cerebral Cortex (New York, N.Y. : 1991)|November 21, 2008
Cortical atrophy and language network reorganization associated with a novel progranulin mutationCarlos Cruchaga, Maria A Fernández-Seara, Manuel Seijo-Martínez, et al.
NPJ Parkinson'S Disease|April 15, 2023
Brainstem neuromelanin and iron MRI reveals a precise signature for idiopathic and LRRK2 Parkinson's diseaseMartín Martínez, Mikel Ariz, Ignacio Alvarez, et al.
Neurobiology of Aging|June 12, 2018
Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish populationMonica Diez-Fairen, Bruno A Benitez, Sara Ortega-Cubero, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.
Dermatitis : Contact, Atopic, Occupational, Drug|March 31, 2023
Patch Testing in Patients With Severe Atopic Dermatitis Treated With Dupilumab: A Multicentric Approach in SpainAlexandre Docampo-Simón, María J Sánchez-Pujol, Maria A Pastor-Nieto, et al.
Parkinsonism & Related Disorders|January 15, 2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter studySara Ortega-Cubero, Oswaldo Lorenzo-Betancor, Elena Lorenzo, et al.
Acta Neuropathologica|March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseaseJan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
Neurobiology of Aging|November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohortJan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Cerebral Cortex (New York, N.Y. : 1991)|November 21, 2008
Cortical atrophy and language network reorganization associated with a novel progranulin mutationCarlos Cruchaga, Maria A Fernández-Seara, Manuel Seijo-Martínez, et al.
NPJ Parkinson'S Disease|April 15, 2023
Brainstem neuromelanin and iron MRI reveals a precise signature for idiopathic and LRRK2 Parkinson's diseaseMartín Martínez, Mikel Ariz, Ignacio Alvarez, et al.
Neurobiology of Aging|June 12, 2018
Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish populationMonica Diez-Fairen, Bruno A Benitez, Sara Ortega-Cubero, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
Journal of Alzheimer'S Disease : JAD|May 11, 2016
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 MutationsElkin Luis, Alexandra Ortiz, Luis Eudave, et al.
Dermatitis : Contact, Atopic, Occupational, Drug|March 31, 2023
Patch Testing in Patients With Severe Atopic Dermatitis Treated With Dupilumab: A Multicentric Approach in SpainAlexandre Docampo-Simón, María J Sánchez-Pujol, Maria A Pastor-Nieto, et al.
Parkinsonism & Related Disorders|January 15, 2015
TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter studySara Ortega-Cubero, Oswaldo Lorenzo-Betancor, Elena Lorenzo, et al.
Acta Neuropathologica|March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's diseaseJan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
Neurobiology of Aging|November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohortJan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Parkinsonism & Related Disorders|December 6, 2020
Exome-wide rare variant analysis in familial essential tremorMonica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
Pageof 5