Livia Parodi
Paris, France
Last Updated: 09/26/2026
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Found 10 publications
The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 06, 2022
Individual perception of environmental factors that influence lower limbs spasticity in inherited spastic paraparesis.
Journal: Annals of physical and rehabilitation medicine
Published: March 30, 2022
Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.
Journal: Brain : a journal of neurology
Published: May 09, 2021
Implication of folate deficiency in CYP2U1 loss of function.
Journal: The Journal of experimental medicine
Published: April 20, 2021
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 23, 2020
Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Journal: Neurogenetics
Published: December 04, 2020
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 20, 2020
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex.
Journal: Brain : a journal of neurology
Published: August 06, 2018
Hereditary ataxias and paraparesias: clinical and genetic update.
Journal: Current opinion in neurology
Published: May 31, 2018
Hereditary spastic paraplegia: More than an upper motor neuron disease.
Journal: Revue neurologique
Published: March 02, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026