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Showing results (11-20 of 16) with videos related to

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Behavioral and Brain Functions : BBF|June 7, 2011
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypesAna I Seixas, José Vale, Paula Jorge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2015
Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12Elizabeth E O'Hearn, Hyon S Hwang, Susan E Holmes, et al.
Results in Immunology|August 10, 2016
Constitutive expression of genes encoding notch receptors and ligands in developing lymphocytes, nTreg cells and dendritic cells in the human thymusLuciana Bento-de-Souza, Jefferson R Victor, Luiz C Bento-de-Souza, et al.
Brain : a Journal of Neurology|April 12, 2012
'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterizationMaría García-Murias, Beatriz Quintáns, Manuel Arias, et al.
Cell Reports|October 9, 2025
Rac1 inhibition prevents axonal cytoskeleton dysfunction in transthyretin amyloid polyneuropathyJoana Magalhães, Vítor Pacheco Dias, Jessica Eira, et al.
American Journal of Human Genetics|July 8, 2017
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar AtaxiaAna I Seixas, Joana R Loureiro, Cristina Costa, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Behavioral and Brain Functions : BBF|June 7, 2011
FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypesAna I Seixas, José Vale, Paula Jorge, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2015
Neuropathology and Cellular Pathogenesis of Spinocerebellar Ataxia Type 12Elizabeth E O'Hearn, Hyon S Hwang, Susan E Holmes, et al.
Results in Immunology|August 10, 2016
Constitutive expression of genes encoding notch receptors and ligands in developing lymphocytes, nTreg cells and dendritic cells in the human thymusLuciana Bento-de-Souza, Jefferson R Victor, Luiz C Bento-de-Souza, et al.
Brain : a Journal of Neurology|April 12, 2012
'Costa da Morte' ataxia is spinocerebellar ataxia 36: clinical and genetic characterizationMaría García-Murias, Beatriz Quintáns, Manuel Arias, et al.
Cell Reports|October 9, 2025
Rac1 inhibition prevents axonal cytoskeleton dysfunction in transthyretin amyloid polyneuropathyJoana Magalhães, Vítor Pacheco Dias, Jessica Eira, et al.
American Journal of Human Genetics|July 8, 2017
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar AtaxiaAna I Seixas, Joana R Loureiro, Cristina Costa, et al.
Pageof 2