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Cerebral Cortex (New York, N.Y. : 1991)
|
November 21, 2008
Cortical atrophy and language network reorganization associated with a novel progranulin mutation
Carlos 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 disease
Martín 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 population
Monica 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 variants
Cristina 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 Mutations
Elkin 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 Spain
Alexandre 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 study
Sara 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 disease
Jan 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 cohort
Jan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Parkinsonism & Related Disorders
|
December 6, 2020
Exome-wide rare variant analysis in familial essential tremor
Monica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
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Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Cerebral Cortex (New York, N.Y. : 1991)
|
November 21, 2008
Cortical atrophy and language network reorganization associated with a novel progranulin mutation
Carlos 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 disease
Martín 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 population
Monica 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 variants
Cristina 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 Mutations
Elkin 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 Spain
Alexandre 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 study
Sara 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 disease
Jan 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 cohort
Jan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Parkinsonism & Related Disorders
|
December 6, 2020
Exome-wide rare variant analysis in familial essential tremor
Monica Diez-Fairen, Gabrielle Houle, Sara Ortega-Cubero, et al.
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of 5