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Marta Ferrero

Showing results (21-30 of 27) with videos related to

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Annals of Neurology|October 5, 2017
Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38Marta Manes, Antonella Alberici, Eleonora Di Gregorio, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 29, 2016
Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypesElisa Giorgio, Alessandro Brussino, Elisa Biamino, et al.
Human Genetics|May 18, 2023
Spinocerebellar ataxia 38: structure-function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspotEnza Ferrero, Eleonora Di Gregorio, Marta Ferrero, et al.
Plos One|March 29, 2023
AA-amyloidosis in cats (Felis catus) housed in sheltersFilippo Ferri, Silvia Ferro, Federico Porporato, et al.
Neurobiology of Disease|November 4, 2018
Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicityCecilia Mancini, Eriola Hoxha, Luisa Iommarini, et al.
American Journal of Human Genetics|July 29, 2014
ELOVL5 mutations cause spinocerebellar ataxia 38Eleonora Di Gregorio, Barbara Borroni, Elisa Giorgio, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Annals of Neurology|October 5, 2017
Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38Marta Manes, Antonella Alberici, Eleonora Di Gregorio, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 29, 2016
Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypesElisa Giorgio, Alessandro Brussino, Elisa Biamino, et al.
Human Genetics|May 18, 2023
Spinocerebellar ataxia 38: structure-function analysis shows ELOVL5 G230V is proteotoxic, conformationally altered and a mutational hotspotEnza Ferrero, Eleonora Di Gregorio, Marta Ferrero, et al.
Plos One|March 29, 2023
AA-amyloidosis in cats (Felis catus) housed in sheltersFilippo Ferri, Silvia Ferro, Federico Porporato, et al.
Neurobiology of Disease|November 4, 2018
Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicityCecilia Mancini, Eriola Hoxha, Luisa Iommarini, et al.
American Journal of Human Genetics|July 29, 2014
ELOVL5 mutations cause spinocerebellar ataxia 38Eleonora Di Gregorio, Barbara Borroni, Elisa Giorgio, et al.
Brain : a Journal of Neurology|August 18, 2022
CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASDLisa Pavinato, Andrea Delle Vedove, Diana Carli, et al.
Pageof 3