Beatriz Quintans
Santiago De Compostela, GA, Spain
Last Updated: 09/26/2026
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Found 27 publications
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
Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4).
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 16, 2021
Genetic landscape of Segawa disease in Spain. Long-term treatment outcomes.
Journal: Parkinsonism & related disorders
Published: June 22, 2021
Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4.
Journal: Journal of neurology
Published: September 07, 2020
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36).
Journal: Cerebellum (London, England)
Published: April 10, 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
Primary familial brain calcifications.
Journal: Handbook of clinical neurology
Published: January 13, 2018
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia.
Journal: American journal of human genetics
Published: March 17, 2017
Last Updated: 09/26/2026