A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia.
Mov Disord
2021
36
8
1984-1985
The rare and the common: An Austrian DRPLA family harboring the European haplotype.
Parkinsonism Relat Disord
2021
87
119-121
Familial writer's cramp: a clinical clue for inherited coenzyme Q10 deficiency.
Neurogenetics
2021
22
1
81-86
Atypical presentations of DYT1 dystonia with acute craniocervical onset.
Parkinsonism Relat Disord
2021
83
54-55
A Recurrent EIF2AK2 Missense Variant Causes Autosomal-Dominant Isolated Dystonia.
Ann Neurol
2021
89
6
1257-1258
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study.
Mov Disord
2021
36
8
1959-1964
HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystonia.
Brain
2021
144
9
2610-2615