Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 (Q33315729)

25 July 2017

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2 (English)

1 reference

25 July 2017

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1 reference

Catarina Oliveira

9

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John Anthony Hardy

10

object named as

John Hardy

1 reference

25 July 2017

2

Rita Guerreiro

1 reference

25 July 2017

11

Andrew Singleton

1 reference

25 July 2017

Jose Bras

1

1 reference

25 July 2017

Maria Ribeiro

3

1 reference

25 July 2017

Ana Morgadinho

4

1 reference

25 July 2017

Cristina Januario

5

1 reference

25 July 2017

Margarida Dias

6

1 reference

25 July 2017

Ana Calado

7

1 reference

25 July 2017

Cristina Semedo

8

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25 July 2017

22 January 2008

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25 July 2017

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25 July 2017

8

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25 July 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-8-1

25 July 2017

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cites work

Digenic parkinsonism: investigation of the synergistic effects of PRKN and LRRK2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Understanding the molecular causes of Parkinson's disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Genetics of Parkinson's disease: LRRK2 on the rise

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Novel PINK1 mutations in early-onset parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

alpha-Synuclein locus triplication causes Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Parkinson's disease: mechanisms and models

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

21 June 2018

Genetics of parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Diagnostic criteria for Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

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

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-1

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-1

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-1

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-1

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248204

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

31 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-8-1

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18211709

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2377-8-1

1 reference

Dimensions Publication ID

25 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-8-1

9 September 2019

1 reference

25 July 2017

1 reference