Linkage exclusion in French families with probable Parkinson's disease (Q57605955)

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2 November 2019

title

Linkage exclusion in French families with probable Parkinson's disease (English)

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Linkage exclusion in French families with probable Parkinson' s disease (English)

1 reference

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2 November 2019

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Marie-Christine Chartier-Harlin

object named as

Marie-Christine Chartier-Harlin

series ordinal

11

1 reference

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2 November 2019

Philippe Amouyel

10

1 reference

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2 November 2019

9

John Hardy

J Hardy

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2 November 2019

7

Luc Defebvre

L Defebvre

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2 November 2019

1

Matt Farrer

M Farrer

1 reference

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2 November 2019

5

Vincent Mouroux

V Mouroux

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2 November 2019

6

Florence Richard

F Richard

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2 November 2019

2

Alain Destée

A Destée

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Fabienne Wavrant De Vrieze

2 November 2019

series ordinal

4

object named as

Fabienne Wavrant‐De Vrièze

F Wavrant-De Vrièze

1 reference

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2 November 2019

8

Sarah Lincoln

S Lincoln

1 reference

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2 November 2019

author name string

Estelle Becquet

series ordinal

3

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2 November 2019

language of work or name

English

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publication date

November 2000

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1 November 2000

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2 November 2019

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2 November 2019

volume

15

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2 November 2019

issue

6

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2 November 2019

page(s)

1075-1083

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Parkinson's disease. First of two parts

2 November 2019

cites work

1 reference

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The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

21 January 2018

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Diagnostic criteria for Parkinson disease

21 January 2018

1 reference

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Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

21 January 2018

1 reference

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Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

21 January 2018

1 reference

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alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

21 January 2018

1 reference

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A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

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The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

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A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor

21 January 2018

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

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Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

21 January 2018

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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

21 January 2018

1 reference

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Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

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Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

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Prevalence of parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease

21 January 2018

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The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

21 January 2018

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Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

21 January 2018

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Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease

21 January 2018

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Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.

21 January 2018

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PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

21 January 2018

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Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

21 January 2018

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Diagnostic criteria for essential tremor: a population perspective.

21 January 2018

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