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Giulia Coarelli

Showing results (61-70 of 72) with videos related to

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BMC Medicine|March 25, 2026
Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disordersMehrdad A Estiar, Eric Yu, Parizad Varghaei, et al.
Brain : a Journal of Neurology|October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3Emilien Petit, Giulia Coarelli, David Morgan, et al.
Journal of Neurology|June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxiasEmilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Neurology|May 10, 2019
Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with <i>SPG7</i>Giulia Coarelli, Rebecca Schule, Bart P C van de Warrenburg, et al.
European Journal of Neurology|July 31, 2025
The Two Faces of Pediatric SCA2Nicolas Rive Le Gouard, Maissa G Bah, Giulia Coarelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
The Journal of Experimental Medicine|September 21, 2021
Implication of folate deficiency in CYP2U1 loss of functionClaire Pujol, Anne Legrand, Livia Parodi, et al.
European Journal of Neurology|June 28, 2025
Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and CharacteristicsJulian Theuriet, Lukas Paulet, Blandine Acket, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-AtaxiaJason W Robertson, Isaac Adanyeguh, David J Arpin, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
BMC Medicine|March 25, 2026
Digenic inheritance of mutations in SPG7 and AFG3L2 causes motor neuron and cerebellar disordersMehrdad A Estiar, Eric Yu, Parizad Varghaei, et al.
Brain : a Journal of Neurology|October 28, 2025
Predictive models for ataxia progression and conversion in spinocerebellar ataxia type 1 and 3Emilien Petit, Giulia Coarelli, David Morgan, et al.
Journal of Neurology|June 1, 2024
SARA captures disparate progression and responsiveness in spinocerebellar ataxiasEmilien Petit, Tanja Schmitz-Hübsch, Giulia Coarelli, et al.
Neurology|May 10, 2019
Loss of paraplegin drives spasticity rather than ataxia in a cohort of 241 patients with <i>SPG7</i>Giulia Coarelli, Rebecca Schule, Bart P C van de Warrenburg, et al.
European Journal of Neurology|July 31, 2025
The Two Faces of Pediatric SCA2Nicolas Rive Le Gouard, Maissa G Bah, Giulia Coarelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
Ebiomedicine|December 24, 2025
Brain atrophy staging in spinocerebellar ataxia type 3 for clinical prognosis and trial enrichmentHannah Baumeister, Philipp Wegner, Mónica Ferreira, et al.
The Journal of Experimental Medicine|September 21, 2021
Implication of folate deficiency in CYP2U1 loss of functionClaire Pujol, Anne Legrand, Livia Parodi, et al.
European Journal of Neurology|June 28, 2025
Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and CharacteristicsJulian Theuriet, Lukas Paulet, Blandine Acket, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2026
A Severity-Agnostic Atrophy Pattern in Spinocerebellar Ataxia Type 3: Volumetrics from ENIGMA-AtaxiaJason W Robertson, Isaac Adanyeguh, David J Arpin, et al.
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