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Sixty hertz pallidal deep brain stimulation for primary torsion dystonia

Neurology, 2007-08, Vol.69 (7), p.681

2007

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Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites

Neurology, 2012-02, Vol.78 (9), p.649

2012

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Etiology of musician's dystonia: familial or environmental?

Neurology, 2009-04, Vol.72 (14), p.1248

2009

Volltextzugriff (PDF)

Olfactory dysfunction in LRRK2 G2019S mutation carriers

Neurology, 2011-07, Vol.77 (4), p.319

2011

Volltextzugriff (PDF)

Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation

Neurology, 2005-01, Vol.64 (2), p.347

2005

Volltextzugriff (PDF)

Gender differences in the risk of familial parkinsonism: Beyond LRRK2?

Neuroscience letters, 2011-06, Vol.496 (2), p.125-128

2011

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The DYT1 phenotype and guidelines for diagnostic testing

Neurology, 2000-05, Vol.54 (9), p.1746

2000

Volltextzugriff (PDF)

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease

Neurology, 2004-02, Vol.62 (3), p.389

2004

Volltextzugriff (PDF)

Age at onset as a factor in determining the phenotype of primary torsion dystonia

Neurology, 2004-10, Vol.63 (8), p.1423

2004

Volltextzugriff (PDF)

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations

Neurology, 2002-04, Vol.58 (8), p.1239

2002

Volltextzugriff (PDF)

Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers

Neurology, 2007-02, Vol.68 (7), p.522

2007

Volltextzugriff (PDF)

Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

Neurology, 2004-08, Vol.63 (4), p.631

2004

Volltextzugriff (PDF)

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening

Neurology, 2005-03, Vol.64 (5), p.908

2005

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Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence

Neurology, 2002-01, Vol.58 (2), p.242

2002

Volltextzugriff (PDF)

Sensory abnormalities in unaffected relatives in familial adult-onset dystonia

Neurology, 2005-09, Vol.65 (6), p.938

2005

Volltextzugriff (PDF)

The early-onset torsion dystonia gene ( DYT1 ) encodes an ATP-binding protein

Nature genetics, 1997-09, Vol.17 (1), p.40-48

1997

Volltextzugriff (PDF)

Mutations in DYT1: extension of the phenotypic and mutational spectrum

Neurology, 2004-02, Vol.62 (3), p.395

2004

Volltextzugriff (PDF)

Analysis of blink rate patterns in normal subjects

Movement disorders, 1997-11, Vol.12 (6), p.1028-1034

1997

Volltextzugriff (PDF)

Gender differences in the IL6 −174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's disease

Neuroscience letters, 2012-01, Vol.506 (2), p.312-316

2012

Volltextzugriff (PDF)

Diagnostic criteria for dystonia in DYT1 families

Neurology, 2002-12, Vol.59 (11), p.1780

2002

Volltextzugriff (PDF)

Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease

Parkinsonism & related disorders, 2013-02, Vol.19 (2), p.186-191

2013

Volltextzugriff (PDF)

Functional brain networks in DYT1 dystonia

Annals of neurology, 1998-09, Vol.44 (3), p.303-312

1998

Volltextzugriff (PDF)

Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families

Annals of neurology, 1997-10, Vol.42 (4), p.670-673

1997

Volltextzugriff (PDF)

Dystonia: Phenotypes and genotypes

Revue neurologique, 2003-10, Vol.159 (10), p.849-856

BRESSMAN, S. B

2003

Volltextzugriff (PDF)

Classification of dystonia

Advances in neurology, 1998, Vol.78, p.1

1998

Volltextzugriff (PDF)

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Sixty hertz pallidal deep brain stimulation for primary torsion dystonia

Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites

Etiology of musician's dystonia: familial or environmental?

Olfactory dysfunction in LRRK2 G2019S mutation carriers

Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation

Gender differences in the risk of familial parkinsonism: Beyond LRRK2?

The DYT1 phenotype and guidelines for diagnostic testing

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease

Age at onset as a factor in determining the phenotype of primary torsion dystonia

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations

Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers

Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening

Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence

Sensory abnormalities in unaffected relatives in familial adult-onset dystonia

The early-onset torsion dystonia gene ( DYT1 ) encodes an ATP-binding protein

Mutations in DYT1: extension of the phenotypic and mutational spectrum

Analysis of blink rate patterns in normal subjects

Gender differences in the IL6 −174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's disease

Diagnostic criteria for dystonia in DYT1 families

Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease

Functional brain networks in DYT1 dystonia

Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families

Dystonia: Phenotypes and genotypes

Classification of dystonia

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