Marta Vela-Correa

Sevilla, AN, Spain

Last Updated: 09/26/2026

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Found 12 publications

NKX2-1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea.

NKX2-1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: March 27, 2026

Deep Brain Stimulation in Children and Adolescents with ε-Sarcoglycan Myoclonus Dystonia Causes a Sustained Improvement in Motor Functionality and Quality of Life.

Deep Brain Stimulation in Children and Adolescents with ε-Sarcoglycan Myoclonus Dystonia Causes a Sustained Improvement in Motor Functionality and Quality of Life.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: February 03, 2025

Early recognition of SGCE-myoclonus-dystonia in children.

Early recognition of SGCE-myoclonus-dystonia in children.

Journal: Developmental medicine and child neurology

Published: November 30, 2021

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients.

Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients.

Journal: Stem cell research

Published: February 10, 2021

ε-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene.

ε-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene.

Journal: Molecular neurobiology

Published: February 09, 2021

PRKRA-Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum.

PRKRA-Related Disorders: Bilateral Striatal Degeneration in Addition to DYT16 Spectrum.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: August 28, 2020

Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated Neurodegeneration.

Fosmetpantotenate Randomized Controlled Trial in Pantothenate Kinase-Associated Neurodegeneration.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 18, 2020

Tic disorders and premonitory urges: validation of the Spanish-language version of the Premonitory Urge for Tics Scale in children and adolescents.

Tic disorders and premonitory urges: validation of the Spanish-language version of the Premonitory Urge for Tics Scale in children and adolescents.

Journal: Neurologia

Published: May 08, 2020

Tic disorders and premonitory urges: validation of the Spanish-language version of the Premonitory Urge for Tics Scale in children and adolescents.

Tic disorders and premonitory urges: validation of the Spanish-language version of the Premonitory Urge for Tics Scale in children and adolescents.

Journal: Neurologia

Published: May 08, 2020

Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene.

Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene.

Journal: Journal of inherited metabolic disease

Published: April 03, 2020

Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.

Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.

Journal: Annals of clinical and translational neurology

Published: March 06, 2020

Delineating the motor phenotype of SGCE-myoclonus dystonia syndrome.

Delineating the motor phenotype of SGCE-myoclonus dystonia syndrome.

Journal: Parkinsonism & related disorders

Published: February 03, 2020

Showing 1-12 of 12

Last Updated: 09/26/2026