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Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic forms

Cellular and molecular life sciences : CMLS, 2004-07, Vol.61 (14), p.1729-1750

2004

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EPA-0225 – Neuropsychiatric phenotype of beta-propeller protein-associated neurodegeneration (BPAN)

European psychiatry, 2014, Vol.29, p.1-1

2014

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Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

The Lancet (British edition), 1998-10, Vol.352 (9137), p.1355-1356

1998

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PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

Neurology, 2004-10, Vol.63 (8), p.1482-1485

2004

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Parkinsonism after Chronic Exposure to the Fungicide Maneb (Manganese ethylene-bis-dithiocarbamate)

Scandinavian Journal of Work, Environment ＆ Health, 1994-08, Vol.20 (4), p.301-305

1994

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Generalized dystonia of early onset associated with a homozygous loss-of-function variant in the AOPEP gene

Parkinsonism & related disorders, 2023-08, Vol.113

2023

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The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson’s disease in European populations

Journal of medical genetics, 2006-07, Vol.43 (7), p.557-562

2006

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A study of five candidate genes in Parkinson’s disease and related neurodegenerative disorders

Neurology, 1999-10, Vol.53 (7), p.1415-1415

1999

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Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease

Journal of medical genetics, 2004-12, Vol.41 (12), p.900-907

2004

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Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism

Neurology, 2003-11, Vol.61 (10), p.1429-1431

2003

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Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Neurology, 2001-09, Vol.57 (5), p.924-927

2001

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Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Science (American Association for the Advancement of Science), 2003-01, Vol.299 (5604), p.256-259

2003

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Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Human mutation, 2013-09, Vol.34 (9), p.1208-1215

2013

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Risperidone for hallucinations in levodopa-treated Parkinson's disease patients

The Lancet (British edition), 1994-05, Vol.343 (8909), p.1370-1371

1994

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Donepezil in the treatment of progressive supranuclear palsy

Acta neurologica Scandinavica, 2001-02, Vol.103 (2), p.123-125

2001

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Smoking habits in multiple system atrophy and progressive supranuclear palsy

Neurology, 2000-01, Vol.54 (1), p.114-114

2000

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Risperidone in levodopa-induced psychosis in advanced parkinson's disease: An open-label, long-term study

Movement disorders, 1997-07, Vol.12 (4), p.610-612

1997

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PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions

Neurology, 2012-08, Vol.79 (8), p.777-784

2012

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Cognitive improvement during Tolcapone treatment in Parkinson's disease

Journal of Neural Transmission, 1997-01, Vol.104 (8-9), p.887-894

1997

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2.102 Sub-cellular localization studies of LRRK2, a brain-specific protein

Parkinsonism & related disorders, 2007, Vol.13, p.S92-S92

2007

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Direct genetic evidence for involvement of tau in progressive supranuclear palsy

Neurology, 1998-10, Vol.51 (4), p.982-985

1998

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Buspirone in levodopa-induced dyskinesias

Clinical neuropharmacology, 1994-02, Vol.17 (1), p.73-82

1994

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Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project

PloS one, 2023-10, Vol.18 (10), p.e0292180

2023

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Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

The New England journal of medicine, 2000-05, Vol.342 (21), p.1560-1567

2000

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Unraveling the pathogenesis of Parkinson's disease--the contribution of monogenic forms

EPA-0225 – Neuropsychiatric phenotype of beta-propeller protein-associated neurodegeneration (BPAN)

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

Parkinsonism after Chronic Exposure to the Fungicide Maneb (Manganese ethylene-bis-dithiocarbamate)

Generalized dystonia of early onset associated with a homozygous loss-of-function variant in the AOPEP gene

The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson’s disease in European populations

A study of five candidate genes in Parkinson’s disease and related neurodegenerative disorders

Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease

Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism

Risperidone for hallucinations in levodopa-treated Parkinson's disease patients

Donepezil in the treatment of progressive supranuclear palsy

Smoking habits in multiple system atrophy and progressive supranuclear palsy

Risperidone in levodopa-induced psychosis in advanced parkinson's disease: An open-label, long-term study

PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions

Cognitive improvement during Tolcapone treatment in Parkinson's disease

2.102 Sub-cellular localization studies of LRRK2, a brain-specific protein

Direct genetic evidence for involvement of tau in progressive supranuclear palsy

Buspirone in levodopa-induced dyskinesias

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project

Dopaminergic neuronal imaging in genetic Parkinson's disease: insights into pathogenesis

Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

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