(Q37178950)

18 August 2017

PINK1 mutations and parkinsonism (English)

1 reference

18 August 2017

1 reference

R Elango

7

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L Ishihara-Paul

series ordinal

1

object named as

L Ishihara-Paul

1 reference

18 August 2017

2

M M Hulihan

1 reference

18 August 2017

3

J Kachergus

1 reference

18 August 2017

4

R Upmanyu

1 reference

18 August 2017

5

L Warren

1 reference

18 August 2017

6

R Amouri

1 reference

18 August 2017

8

R K Prinjha

1 reference

18 August 2017

9

A Soto

1 reference

18 August 2017

10

M Kefi

1 reference

18 August 2017

11

M Zouari

1 reference

18 August 2017

12

S B Sassi

1 reference

18 August 2017

13

S B Yahmed

1 reference

18 August 2017

14

G El Euch-Fayeche

1 reference

18 August 2017

15

P M Matthews

1 reference

18 August 2017

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L T Middleton

1 reference

18 August 2017

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R A Gibson

1 reference

18 August 2017

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F Hentati

1 reference

18 August 2017

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M J Farrer

1 reference

18 August 2017

PMC publication ID

2676945

language of work or name

English

0 references

publication date

6 August 2008

1 reference

18 August 2017

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18 August 2017

71

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18 August 2017

12

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18 August 2017

896-902

1 reference

Impaired dopamine release and synaptic plasticity in the striatum of PINK1-deficient mice

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Motor subtype and cognitive decline in Parkinson's disease, Parkinson's disease with dementia, and dementia with Lewy bodies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Genetics of Parkinson disease: paradigm shifts and future prospects.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological 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=2676945

Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET 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=2676945

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

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=2676945

Clinical and genetic study of familial Parkinson's disease in Tunisia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Parkinsonism: onset, progression, and mortality

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

A simple salting out procedure for extracting DNA from human nucleated cells

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

A New Method for Measuring Daytime Sleepiness: The Epworth Sleepiness Scale

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic 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=2676945

Silencing of the Pink1 gene expression by conditional RNAi does not induce dopaminergic neuron death in mice.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive 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=2676945

Validity of a modified Parkinson's disease screening questionnaire in India: effects of literacy of participants and medical training of screeners and implications for screening efforts in developing countries.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Parkin variants in North American Parkinson's disease: cases and controls.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

Lrrk2 pathogenic substitutions in Parkinson's disease

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2676945

4 December 2018

1 reference

12 December 2020

Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?

1 reference

PubMed

12 December 2020

A heterozygous effect for PINK1 mutations in Parkinson's disease?

1 reference

PubMed

12 December 2020

Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum

1 reference

PubMed

12 December 2020

10.1212/01.WNL.0000323812.40708.1F

Identifiers

DOI

1 reference

18 August 2017

1 reference

PMC publication ID

2676945

18 August 2017

PubMed publication ID

18685134

1 reference

PMC publication ID

2676945