(Q44696634)

5 December 2017

Genetic assessment of familial and early-onset Parkinson's disease in a Greek population (English)

1 reference

5 December 2017

1 reference

M Bozi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

D Papadimitriou

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

R Antonellou

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

M Moraitou

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

M Maniati

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

D K Vassilatis

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A Leonardos

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

G Tagaris

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

G Malamis

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

D Theofilopoulos

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

S Kamakari

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

E Stamboulis

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A Athanassiadou

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

H Michelakakis

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

A Papadimitriou

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

T Gasser

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

L Stefanis

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

publication date

7 December 2013

1 reference

European Journal of Neurology

5 December 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

page(s)

963-968

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

10 June 2020

cites work

1 reference

LRRK2 G2019S in the North African population: a review

21 January 2018

1 reference

Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India

21 January 2018

1 reference

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel α-synuclein missense mutation in Parkinson disease

21 January 2018

1 reference

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?

21 January 2018

1 reference

Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein

21 January 2018

1 reference

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

21 January 2018

1 reference

Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece

21 January 2018

1 reference

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa

21 January 2018

1 reference

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

21 January 2018

1 reference

Is the G2019S LRRK2 mutation common in all southern European populations?

21 January 2018

1 reference

LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP.

21 January 2018

1 reference

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

21 January 2018

1 reference

Locus-specific mutation databases for neurodegenerative brain diseases

21 January 2018

1 reference

High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease.

21 January 2018

1 reference

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study

21 January 2018

1 reference

Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: an independent pathogenic role.

21 January 2018

1 reference

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

21 January 2018

1 reference

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

21 January 2018

1 reference

How much phenotypic variation can be attributed to parkin genotype?

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/ENE.12315

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24313877%20AND%20SRC:MED&resulttype=core&format=json

10 June 2020

1 reference