(Q34470633)

2 August 2017

Genetics of Parkinson's disease: LRRK2 on the rise (English)

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2 August 2017

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1

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language of work or name

English

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publication date

1 December 2005

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2 August 2017

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2 August 2017

128

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2 August 2017

2760-2762

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2 August 2017

Pt 12

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PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation

2 August 2017

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

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/10.1093%2FBRAIN%2FAWH676

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Parkinson's disease: from causes to mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

A common LRRK2 mutation in idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

LRRK2 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWH676

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWH676

1 reference

2 August 2017

1 reference

PubMed ID

16311269