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Mario Fichera

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

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Movement Disorders : Official Journal of the Movement Disorder Society|February 17, 2023
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar AtaxiaLorenzo Nanetti, Stefania Magri, Mario Fichera, et al.
Frontiers in Neurology|January 24, 2022
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic <i>PNPLA6</i> Gene Variants: Eight Novel Cases and Review of the LiteratureLorenzo Nanetti, Daniela Di Bella, Stefania Magri, et al.
Human Molecular Genetics|January 11, 2022
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1Andrea Quatrana, Elena Morini, Francesca Tiano, et al.
Annals of Clinical and Translational Neurology|August 29, 2023
Longitudinal changes of SARA scale in Friedreich ataxia: Strong influence of baseline score and age at onsetLuca Porcu, Mario Fichera, Lorenzo Nanetti, et al.
Human Molecular Genetics|January 17, 2020
Frataxin deficiency in Friedreich's ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survivalFrancesca Tiano, Francesca Amati, Fabio Cherubini, et al.
Scientific Reports|November 10, 2022
Prediction of the disease course in Friedreich ataxiaChristian Hohenfeld, Ulrich Terstiege, Imis Dogan, et al.
Pageof 2

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.
Movement Disorders : Official Journal of the Movement Disorder Society|February 17, 2023
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar AtaxiaLorenzo Nanetti, Stefania Magri, Mario Fichera, et al.
Frontiers in Neurology|January 24, 2022
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic <i>PNPLA6</i> Gene Variants: Eight Novel Cases and Review of the LiteratureLorenzo Nanetti, Daniela Di Bella, Stefania Magri, et al.
Human Molecular Genetics|January 11, 2022
Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1Andrea Quatrana, Elena Morini, Francesca Tiano, et al.
Annals of Clinical and Translational Neurology|August 29, 2023
Longitudinal changes of SARA scale in Friedreich ataxia: Strong influence of baseline score and age at onsetLuca Porcu, Mario Fichera, Lorenzo Nanetti, et al.
Human Molecular Genetics|January 17, 2020
Frataxin deficiency in Friedreich's ataxia is associated with reduced levels of HAX-1, a regulator of cardiomyocyte death and survivalFrancesca Tiano, Francesca Amati, Fabio Cherubini, et al.
Scientific Reports|November 10, 2022
Prediction of the disease course in Friedreich ataxiaChristian Hohenfeld, Ulrich Terstiege, Imis Dogan, et al.
Pageof 2