Correction: A case of novel DYT6 dystonia variant with serious complications after deep brain stimulation therapy: a case report.
BMC Neurol
2022
22
1
A case of novel DYT6 dystonia variant with serious complications after deep brain stimulation therapy: a case report.
BMC Neurol
2022
22
1
METHYLGLYOXAL - A CENTRAL METABOLIC FACTOR IN RESTLESS LEGS SYNDROME?
Sleep Med
2022
100 Suppl 1
S231-S231
Beyond founder and truncting variants in TECPR2-associated disorder
Eur J Hum Genet
2022
30 Suppl 1
SUPPL 1
254-255
Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes.
Ann Neurol
2022
91
2
225-237
A de novo BCL11B variant case manifesting with dystonic movement disorder regarding the article "BCL11B-related disorder in two canadian children: Expanding the clinical phenotype (Prasad et al., 2020).".
Eur J Med Genet
2022
65
11
Genetic intersection between dystonia and neurodevelopmental disorders: Insights from genomic sequencing.
Parkinsonism Relat Disord
2022
102
131-140
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders: More Common than Expected.
Mov Disord
2022
37
11
2323-2324
Progressive choreodystonia in X-linked hyper-IgM immunodeficiency: a rare but recurrent presentation.
Ann Clin Transl Neurol
2022
9
4
577-581
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.
Parkinsonism Relat Disord
2022
97
52-56