Christina Fevga
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Segmental dystonia as the prominent phenotype resulting from a MICU1 splice variant in a new Indian case.
Journal: Parkinsonism & related disorders
Published: July 21, 2022
Isolated Paroxysmal Non-kinesigenic Dystonia Associated with Homozygous PDHB Variant in an Indian Family.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 30, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
Journal: Brain : a journal of neurology
Published: March 29, 2022
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia.
Journal: Brain communications
Published: February 14, 2022
AOPEP Homozygous Loss-of-Function Variant in an Indian Patient with Early-Onset Generalized Dystonia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 23, 2021
A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease.
Journal: Parkinsonism & related disorders
Published: March 17, 2021
EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.
Journal: Annals of neurology
Published: September 09, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026