Maria-jesus J. Sobrido
A Coruna, GA, Spain
Last Updated: 09/26/2026
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Found 43 publications
A nop56 Zebrafish Loss-of-Function Model Exhibits a Severe Neurodegenerative Phenotype.
Journal: Biomedicines
Published: July 06, 2022
SPG46 spastic paraplegia due to GBA2 mutation: description of the first case in Spain.
Journal: Neurologia
Published: April 21, 2022
Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study.
Journal: Journal of neurology
Published: October 30, 2021
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 29, 2021
Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4).
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 16, 2021
Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.
Journal: Journal of neurology
Published: September 07, 2020
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36.
Journal: Neuron
Published: December 03, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Journal: American journal of human genetics
Published: June 08, 2019
Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: first families detected in Spain.
Journal: Neurologia
Published: December 28, 2018
Autosomal recessive spinocerebellar ataxia SCAR8/ARCA1: First families detected in Spain.
Journal: Neurologia
Published: December 28, 2018
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Journal: American journal of human genetics
Published: December 09, 2018
Last Updated: 09/26/2026