(Q37180446)

18 August 2017

A multidisciplinary study of patients with early-onset PD with and without parkin mutations (English)

1 reference

18 August 2017

13

A Brice

0 references

Bruno Dubois

French Parkinson's Disease Genetics Study Group

9

object named as

B Dubois

0 references

14

object named as

French Parkinson's Disease Genetics Study Group

1 reference

18 August 2017

12

Y Agid

1 reference

18 August 2017

4

E Broussolle

1 reference

18 August 2017

2

S Thobois

1 reference

Sophie Tezenas du Montcel

18 August 2017

5

object named as

S Tezenas du Montcel

1 reference

18 August 2017

E Lohmann

1

1 reference

18 August 2017

S Lesage

3

1 reference

18 August 2017

M-J Ribeiro

6

1 reference

18 August 2017

P Remy

7

1 reference

18 August 2017

A Pelissolo

8

1 reference

18 August 2017

L Mallet

10

1 reference

18 August 2017

P Pollak

11

1 reference

18 August 2017

language of work or name

English

0 references

publication date

5 November 2008

1 reference

18 August 2017

1 reference

18 August 2017

72

1 reference

18 August 2017

2

1 reference

18 August 2017

110-116

1 reference

Deciphering the role of heterozygous mutations in genes associated with parkinsonism

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Evolution of cognitive dysfunction in an incident Parkinson's disease cohort.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Proposed dose equivalence for rapid switch between dopamine receptor agonists in Parkinson's disease: a review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

How much phenotypic variation can be attributed to parkin genotype?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Complex relationship between Parkin mutations and Parkinson disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Alpha-synuclein and Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Association between early-onset Parkinson's disease and mutations in the parkin gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

The nigrostriatal dopaminergic system in familial early onset parkinsonism with parkin mutations.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Dopa-responsive dystonia: [18F]dopa positron emission tomography.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Parkin disease: a phenotypic study of a large case series

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2677494

Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls

3 September 2018

1 reference

12 December 2020

Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease

1 reference

12 December 2020

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

1 reference

12 December 2020

Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years

1 reference

12 December 2020

10.1212/01.WNL.0000327098.86861.D4

Identifiers

DOI

1 reference

18 August 2017

1 reference

18 August 2017

1 reference