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EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood

European journal of neurology, 2014-04, Vol.21 (4), p.552-562

2014

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Characterization of social cognition impairment in multiple sclerosis

European journal of neurology, 2018-01, Vol.25 (1), p.90-96

2018

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Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease

European journal of neurology, 2020-02, Vol.27 (2), p.273-279

2020

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Auditory time perception in Huntington's disease

Neuropsychologia, 2018-10, Vol.119, p.247-252

2018

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Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China

Neuroscience letters, 2010-01, Vol.469 (2), p.256-259

2010

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EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders

European journal of neurology, 2011-02, Vol.18 (2), p.207-217

2011

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PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China

European journal of neurology, 2014-01, Vol.21 (1), p.174-176

2014

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Nature genetics, 1999-11, Vol.23 (3), p.296-303

1999

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EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

European journal of neurology, 2009-07, Vol.16 (7), p.777-785

2009

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Circadian patterns of neurotransmitter related gene expression in motor regions of the rat brain

Neuroscience letters, 2004-03, Vol.358 (1), p.17-20

2004

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Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls

European journal of neurology, 2014-04, Vol.21 (4), p.637-642

2014

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EFNS guidelines on the molecular diagnosis of mitochondrial disorders

European journal of neurology, 2009-12, Vol.16 (12), p.1255-1264

2009

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LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

European journal of neurology, 2008-03, Vol.15 (3), p.301-305

2008

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Bilateral stimulation of globus pallidus internus for treatment of cervical dystonia

The Lancet (British edition), 1999-09, Vol.354 (9181), p.837-838

1999

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Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort

European journal of neurology, 2012-06, Vol.19 (6), p.924-926

2012

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EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias

European journal of neurology, 2010-02, Vol.17 (2), p.179-188

2010

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Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China

European journal of neurology, 2010-06, Vol.17 (6), p.846-851

2010

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Pallidal deep brain stimulation in patients with cervical dystonia and severe cervical dyskinesias with cervical myelopathy

Journal of neurology, neurosurgery and psychiatry, 2002-02, Vol.72 (2), p.249-256

2002

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Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand

Neuroscience, 2007-03, Vol.145 (3), p.1026-1036

2007

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

Human molecular genetics, 2000-03, Vol.9 (4), p.637-644

2000

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EFNS review on the role of muscle biopsy in the investigation of myalgia

European journal of neurology, 2013-07, Vol.20 (7), p.997-1005

2013

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Effect of chronic pallidal deep brain stimulation on off period dystonia and sensory symptoms in advanced Parkinson’s disease

Journal of neurology, neurosurgery and psychiatry, 2002-10, Vol.73 (4), p.395-399

2002

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Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese population

Neuroscience letters, 2008-09, Vol.442 (3), p.200-202

2008

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U7 snRNAs induce correction of mutated dystrophin pre-mRNA by exon skipping

Cellular and molecular life sciences : CMLS, 2003-03, Vol.60 (3), p.557-566

2003

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A novel dominant mutation of the Nav1.4 alpha-subunit domain I leading to sodium channel myotonia

Neurology, 2008-11, Vol.71 (21), p.1669

2008

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EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood

Characterization of social cognition impairment in multiple sclerosis

Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease

Auditory time perception in Huntington's disease

Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders

PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias

Circadian patterns of neurotransmitter related gene expression in motor regions of the rat brain

Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls

EFNS guidelines on the molecular diagnosis of mitochondrial disorders

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

Bilateral stimulation of globus pallidus internus for treatment of cervical dystonia

Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort

EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias

Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China

Pallidal deep brain stimulation in patients with cervical dystonia and severe cervical dyskinesias with cervical myelopathy

Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

EFNS review on the role of muscle biopsy in the investigation of myalgia

Effect of chronic pallidal deep brain stimulation on off period dystonia and sensory symptoms in advanced Parkinson’s disease

Lack of evidence for association of a UCH-L1 S18Y polymorphism with Parkinson's disease in a Han-Chinese population

U7 snRNAs induce correction of mutated dystrophin pre-mRNA by exon skipping

A novel dominant mutation of the Nav1.4 alpha-subunit domain I leading to sodium channel myotonia

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