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Etiology of musician's dystonia: familial or environmental?

Neurology, 2009-04, Vol.72 (14), p.1248-1254

2009

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Olfactory dysfunction in LRRK2 G2019S mutation carriers

Neurology, 2011-07, Vol.77 (4), p.319-324

2011

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Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study

Neurology, 2012-05, Vol.78 (18), p.1434-1440

2012

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

Neurology, 2005-01, Vol.64 (2), p.347-349

2005

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Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia

Neurology, 2009-06, Vol.72 (24), p.2097-2103

2009

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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.1746-1753

2000

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

Neurology, 2004-02, Vol.62 (3), p.389-394

2004

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

Neurology, 2002-04, Vol.58 (8), p.1239-1246

2002

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Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

Neurology, 2004-08, Vol.63 (4), p.631-637

2004

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

Neurology, 2007-02, Vol.68 (7), p.522-524

2007

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

Neurology, 2005-03, Vol.64 (5), p.908-911

2005

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The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease

Journal of neurology, 2015-11, Vol.262 (11), p.2443-2447

2015

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

Neurology, 2002-01, Vol.58 (2), p.242-245

2002

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Regional metabolism in primary torsion dystonia: effects of penetrance and genotype

Neurology, 2004-04, Vol.62 (8), p.1384-1390

2004

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Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease

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

2013

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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

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Sensory abnormalities in unaffected relatives in familial adult-onset dystonia

Neurology, 2005-09, Vol.65 (6), p.938-940

2005

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Mutations in DYT1: extension of the phenotypic and mutational spectrum

Neurology, 2004-02, Vol.62 (3), p.395-400

2004

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Diagnostic criteria for dystonia in DYT1 families

Neurology, 2002-12, Vol.59 (11), p.1780-1782

2002

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Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study

Neurology, 2011-01, Vol.76 (4), p.319-326

2011

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Dominantly transmitted focal dystonia in families of patients with musician's cramp

Neurology, 2006-08, Vol.67 (4), p.691-693

2006

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Dystonia: Phenotypes and genotypes

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

BRESSMAN, S. B

2003

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Classification of dystonia

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

1998

Volltextzugriff (PDF)

Dystonia update

Clinical neuropharmacology, 2000-09, Vol.23 (5), p.239-251

BRESSMAN, Susan B

2000

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Etiology of musician's dystonia: familial or environmental?

Olfactory dysfunction in LRRK2 G2019S mutation carriers

Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study

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

Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia

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

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

Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

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

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

The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease

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

Regional metabolism in primary torsion dystonia: effects of penetrance and genotype

Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease

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

Sensory abnormalities in unaffected relatives in familial adult-onset dystonia

Mutations in DYT1: extension of the phenotypic and mutational spectrum

Diagnostic criteria for dystonia in DYT1 families

Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study

Dominantly transmitted focal dystonia in families of patients with musician's cramp

Dystonia: Phenotypes and genotypes

Classification of dystonia

Dystonia update

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