about
CACNA1B mutation is linked to unique myoclonus-dystonia syndromeWhispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 geneAnalysis of the PINK1 gene in a large cohort of cases with Parkinson disease.Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia.Cognition and psychopathology in myoclonus-dystonia.Anterior subcutaneous transposition for persistent ulnar neuropathy after neurolysis.Impaired health-related quality of life in meningioma patients-a systematic review.Cervical dystonia and genetic common variation in the dopamine pathway.Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?Late-onset Huntington disease with intermediate CAG repeats: true or false?Early nerve repair in traumatic brachial plexus injuries in adults: treatment algorithm and first experiences.Reliability and Validity of the Therapy Intensity Level Scale: Analysis of Clinimetric Properties of a Novel Approach to Assess Management of Intracranial Pressure in Traumatic Brain Injury.Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp.DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.RELN rare variants in myoclonus-dystonia.More outreach for young scientists.Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia.SGCZ mutations are unlikely to be associated with myoclonus dystonia.[DoNTRuN a neurosurgical trainee network; network for the advancement of clinical research].Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystoniaIs TOR1A a risk factor in adult-onset primary torsion dystonia?Phenotypes and genetic architecture of focal primary torsion dystoniaTHAP1 mutations are infrequent in spasmodic dysphoniaA new familial syndrome with dystonia and lower limb action myoclonus
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-1251-4485
@en
name
Justus L Groen
@ast
Justus L Groen
@en
Justus L Groen
@nl
type
label
Justus L Groen
@ast
Justus L Groen
@en
Justus L Groen
@nl
altLabel
Justus Groen
@en
prefLabel
Justus L Groen
@ast
Justus L Groen
@en
Justus L Groen
@nl
P1006
P214
P1006
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P214
P31
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0000-0002-1251-4485
P734
P7859
viaf-309891975