Petra Pavelekova
Kosice, KI, Slovakia
Last Updated: 09/26/2026
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Found 11 publications
Neurophysiological Testing to Diagnose Stiff-Person Spectrum Disorder.
Journal: Movement disorders clinical practice
Published: May 16, 2025
Predictors of whole exome sequencing in dystonic cerebral palsy and cerebral palsy-like disorders.
Journal: Parkinsonism & related disorders
Published: November 20, 2022
Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomes.
Journal: Parkinsonism & related disorders
Published: May 11, 2022
Prevalence of Fabry Disease among Patients with Parkinson's Disease.
Journal: Parkinson's disease
Published: August 23, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia.
Journal: Parkinsonism & related disorders
Published: June 29, 2021
Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series.
Journal: Parkinsonism & related disorders
Published: May 21, 2021
A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 08, 2021
Variant recurrence confirms the existence of a FBXO31-related spastic-dystonic cerebral palsy syndrome.
Journal: Annals of clinical and translational neurology
Published: January 26, 2021
De novo variants in neurodevelopmental disorders-experiences from a tertiary care center.
Journal: Clinical genetics
Published: December 18, 2020
Monogenic variants in dystonia: an exome-wide sequencing study.
Journal: The Lancet. Neurology
Published: March 11, 2020
Atypical presentations of DYT1 dystonia with acute craniocervical onset.
Journal: Parkinsonism & related disorders
Published: August 24, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026