(Q57605955)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

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

0 references

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

Marie-Christine Chartier-Harlin

object named as

Marie-Christine Chartier-Harlin

series ordinal

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Philippe Amouyel

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

9

John Hardy

J Hardy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

7

Luc Defebvre

L Defebvre

1 reference

2 November 2019

1

Matt Farrer

M Farrer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

5

Vincent Mouroux

V Mouroux

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

6

Florence Richard

F Richard

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

2

Alain Destée

A Destée

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

Fabienne Wavrant De Vrieze

2 November 2019

series ordinal

4

object named as

Fabienne Wavrant‐De Vrièze

F Wavrant-De Vrièze

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

8

Sarah Lincoln

S Lincoln

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

Estelle Becquet

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

language of work or name

English

0 references

publication date

November 2000

0 references

1 November 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

1075-1083

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

Parkinson's disease. First of two parts

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

Diagnostic criteria for Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

The ubiquitin pathway in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

Diagnostic criteria for essential tremor: a population perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8257%28200011%2915%3A6%3C1075%3A%3AAID-MDS1004%3E3.0.CO%3B2-2

10.1002/1531-8257(200011)15:6<1075::AID-MDS1004>3.0.CO;2-2

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11104189%20AND%20SRC:MED&resulttype=core&format=json