Lista de obras -

A new familial syndrome with dystonia and lower limb action myoclonus

artículo científico publicado en 2011

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

artículo científico publicado en 2004

Anterior subcutaneous transposition for persistent ulnar neuropathy after neurolysis.

artículo científico publicado en 2017

Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia

artículo científico publicado en 2012

CACNA1B mutation is linked to unique myoclonus-dystonia syndrome

artículo científico publicado en 2015

Cervical dystonia and genetic common variation in the dopamine pathway

artículo científico publicado en 2012

Cognition and psychopathology in myoclonus-dystonia.

artículo científico

DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystonia

artículo científico publicado en 2014

DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation

artículo científico publicado en 2010

DoNTRuN a neurosurgical trainee network; network for the advancement of clinical research

artículo científico publicado en 2018

Early nerve repair in traumatic brachial plexus injuries in adults: treatment algorithm and first experiences.

artículo científico publicado en 2018

Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia.

artículo científico publicado en 2012

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

artículo científico publicado en 2004

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

artículo científico publicado en 2013

Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.

artículo científico publicado en 2009

Impaired health-related quality of life in meningioma patients-a systematic review.

artículo científico publicado en 2016

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

scientific article published on 04 March 2013

Late-onset Huntington disease with intermediate CAG repeats: true or false?

artículo científico publicado en 2010

More outreach for young scientists.

artículo científico publicado en 2010

Phenotypes and genetic architecture of focal primary torsion dystonia

article by Justus L Groen et al published 8 July 2012 in Journal of Neurology, Neurosurgery and Psychiatry

RELN rare variants in myoclonus-dystonia

artículo científico publicado en 2015

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

artículo científico publicado en 2016

SGCZ mutations are unlikely to be associated with myoclonus dystonia.

artículo científico publicado en 2014

Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp

artículo científico publicado en 2009

THAP1 mutations are infrequent in spasmodic dysphonia

artículo científico publicado en 2011

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene

artículo científico publicado en 2013

Lista de obras de

A new familial syndrome with dystonia and lower limb action myoclonus

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

Anterior subcutaneous transposition for persistent ulnar neuropathy after neurolysis.

Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia

CACNA1B mutation is linked to unique myoclonus-dystonia syndrome

Cervical dystonia and genetic common variation in the dopamine pathway

Cognition and psychopathology in myoclonus-dystonia.

DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystonia

DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation

DoNTRuN a neurosurgical trainee network; network for the advancement of clinical research

Early nerve repair in traumatic brachial plexus injuries in adults: treatment algorithm and first experiences.

Genetic and phenotypic heterogeneity in sporadic and familial forms of paroxysmal dyskinesia.

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?

Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.

Impaired health-related quality of life in meningioma patients-a systematic review.

Is TOR1A a risk factor in adult-onset primary torsion dystonia?

Late-onset Huntington disease with intermediate CAG repeats: true or false?

More outreach for young scientists.

Phenotypes and genetic architecture of focal primary torsion dystonia

RELN rare variants in myoclonus-dystonia

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

SGCZ mutations are unlikely to be associated with myoclonus dystonia.

Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp

THAP1 mutations are infrequent in spasmodic dysphonia

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene