(Q35231079)

7 August 2017

Mutations in DJ-1 are rare in familial Parkinson disease (English)

1 reference

7 August 2017

1 reference

9

Tatiana Foroud

0 references

Nathan Pankratz

1

Nathan Pankratz

0 references

Joanne M. Wojcieszek

6

Joanne Wojcieszek

1 reference

7 August 2017

2

Michael W Pauciulo

1 reference

7 August 2017

Veronika E. Elsaesser

3

Veronika E Elsaesser

1 reference

7 August 2017

4

Diane K Marek

1 reference

7 August 2017

5

Cheryl A Halter

1 reference

7 August 2017

7

Alice Rudolph

1 reference

7 August 2017

8

Clifford W Shults

1 reference

Parkinson Study Group - PROGENI Investigators

7 August 2017

11

Parkinson Study Group - PROGENI Investigators

1 reference

7 August 2017

William C Nichols

10

1 reference

7 August 2017

language of work or name

English

0 references

publication date

25 September 2006

1 reference

7 August 2017

1 reference

7 August 2017

408

1 reference

7 August 2017

3

1 reference

7 August 2017

209-213

1 reference

Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

DJ-1 mutations in Parkinson's disease

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. 1992.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

The role of pathogenic DJ-1 mutations in Parkinson's disease.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Absence of previously reported variants in theSCNA (G88C and G209A),NR4A2 (T291D and T245G) and theDJ-1 (T497C) genes in familial Parkinson's disease from theGenePD study

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706076

Genetics of Parkinson's disease

15 November 2018

1 reference

12 December 2020

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

1 reference

12 December 2020

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

1 reference

12 December 2020

The R98Q variation in DJ-1 represents a rare polymorphism

1 reference

12 December 2020

10.1016/J.NEULET.2006.09.003

Identifiers

DOI

1 reference

7 August 2017

1 reference

7 August 2017

1 reference