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

Movement disorders, 2010-10, Vol.25 (14), p.2420-2427

2010

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A randomized controlled trial comparing conservative versus surgical treatment in patients with foot drop due to peroneal nerve entrapment: results of an internal feasibility pilot study

Pilot and feasibility studies, 2023-10, Vol.9 (1), p.1-181, Article 181

2023

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Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?

Molecular brain, 2021-01, Vol.14 (1), p.18-18, Article 18

2021

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Letter to the Editor. Reoperation for recurrent or persistent ulnar nerve symptoms

Journal of neurosurgery, 2019-01, Vol.130 (4), p.1403-1405

2019

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

Movement disorders, 2013-06, Vol.28 (6), p.827-831

2013

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Fusion rates support wired allograft combined with instrumented craniocervical fixation in the paediatric population

Acta neurochirurgica, 2020-05, Vol.162 (5), p.985-991

2020

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Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury

Muscle & nerve, 2023-04, Vol.67 (4), p.314-319

2023

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Endoscopic harvest of sural nerve for grafting in infants with brachial plexus birth injury

The Journal of hand surgery, European volume, 2022-09, Vol.47 (8), p.865-866

2022

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THAP1 mutations are infrequent in spasmodic dysphonia

Movement disorders, 2011-08, Vol.26 (10), p.1952-1954

2011

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

Neuro-oncology (Charlottesville, Va.), 2017-07, Vol.19 (7), p.897-907

2017

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

Journal of neurosurgery, 2019-01, Vol.130 (1), p.172-178

2019

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Letter to the Editor. Nerve repair in brachial plexus birth injury

Journal of neurosurgery. Pediatrics, 2020-10, Vol.27 (1), p.122

2020

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CACNA1B mutation is linked to unique myoclonus-dystonia syndrome

Human molecular genetics, 2015-02, Vol.24 (4), p.987-993

2015

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Surgical Interventions for Cervical Radiculopathy Caused by a Vertebral Artery Loop: A Case Report and Review of the Literature

World neurosurgery, 2020-03, Vol.135, p.28-34

2020

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Early grafting in severe adult traumatic brachial plexus injury

Neurosurgical Focus: Video, 2023-01, Vol.8 (1), p.V13-V13

2023

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Neurofibromas in LZTR1 schwannomatosis

Clinical genetics, 2022-05, Vol.101 (5-6), p.571-572

2022

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

Journal of neurology, 2013-01, Vol.260 (1), p.93-99

2013

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Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia

Journal of neurology, 2015-05, Vol.262 (5), p.1340-1343

2015

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

Movement disorders, 2009-01, Vol.24 (2), p.196-203

2009

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Cognition and psychopathology in myoclonus-dystonia

Journal of neurology, neurosurgery and psychiatry, 2012-08, Vol.83 (8), p.814-820

2012

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RELN rare variants in myoclonus-dystonia

Movement disorders, 2015-03, Vol.30 (3), p.415-419

2015

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Anterior subcutaneous transposition for persistent ulnar neuropathy after neurolysis

Neurosurgical focus, 2017-03, Vol.42 (3), p.E8-E8

2017

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

Journal of neurology, neurosurgery and psychiatry, 2010-02, Vol.81 (2), p.228-230

2010

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

Parkinsonism & related disorders, 2014-07, Vol.20 (7), p.782-785

2014

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More outreach for young scientists

Nature (London), 2010-09, Vol.467 (7314), p.401-401

2010

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

A randomized controlled trial comparing conservative versus surgical treatment in patients with foot drop due to peroneal nerve entrapment: results of an internal feasibility pilot study

Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?

Letter to the Editor. Reoperation for recurrent or persistent ulnar nerve symptoms

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

Fusion rates support wired allograft combined with instrumented craniocervical fixation in the paediatric population

Optimal timing of needle electromyography to diagnose lesion severity in traumatic radial nerve injury

Endoscopic harvest of sural nerve for grafting in infants with brachial plexus birth injury

THAP1 mutations are infrequent in spasmodic dysphonia

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

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

Letter to the Editor. Nerve repair in brachial plexus birth injury

CACNA1B mutation is linked to unique myoclonus-dystonia syndrome

Surgical Interventions for Cervical Radiculopathy Caused by a Vertebral Artery Loop: A Case Report and Review of the Literature

Early grafting in severe adult traumatic brachial plexus injury

Neurofibromas in LZTR1 schwannomatosis

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

Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia

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

Cognition and psychopathology in myoclonus-dystonia

RELN rare variants in myoclonus-dystonia

Anterior subcutaneous transposition for persistent ulnar neuropathy after neurolysis

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

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

More outreach for young scientists

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