Ivelisse Sanchez
Barcelona, CT, Spain
Last Updated: 09/26/2026
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Found 12 publications
Longitudinal analysis shows GAA1 length and baseline clinical status as robust predictors of progression in Friedreich ataxia.
Journal: Journal of neurology
Published: December 17, 2025
Novel genotype-phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC)n insertion in spinocerebellar ataxia type 37.
Journal: Human genetics
Published: August 26, 2023
Correction to: Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia.
Journal: Neurogenetics
Published: November 10, 2021
POLR3A-related spastic ataxia: new mutations and a look into the phenotype.
Journal: Journal of neurology
Published: July 01, 2019
Spectral characterization of laser-accelerated protons with CR-39 nuclear track detector.
Journal: The Review of scientific instruments
Published: March 03, 2018
Clinical, genetic and neuropathological characterization of spinocerebellar ataxia type 37.
Journal: Brain : a journal of neurology
Published: December 18, 2017
Characterization of Alu and recombination-associated motifs mediating a large homozygous SPG7 gene rearrangement causing hereditary spastic paraplegia.
Journal: Neurogenetics
Published: July 09, 2014
Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.
Journal: Cerebellum (London, England)
Published: December 06, 2013
The spinocerebellar ataxias: clinical aspects and molecular genetics.
Journal: Advances in experimental medicine and biology
Published: March 14, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026