(Q84393456)

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5 February 2020

case report

0 references

title

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies (English)

1 reference

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5 February 2020

1 reference

3

1 reference

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5 February 2020

author name string

Carles Gaig

1

1 reference

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5 February 2020

María José Martí

2

1 reference

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5 February 2020

Adriana Cardozo

4

1 reference

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5 February 2020

Maria Jesus Rey

5

1 reference

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5 February 2020

Eduardo Tolosa

6

1 reference

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5 February 2020

publication date

23 January 2009

1 reference

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5 February 2020

1 reference

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5 February 2020

volume

2009

1 reference

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

5 February 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

12 December 2020

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

1 reference

12 December 2020

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

1 reference

12 December 2020

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

1 reference

12 December 2020

Lrrk2 and Lewy body disease

1 reference

12 December 2020

Biochemical and pathological characterization of Lrrk2.

1 reference

12 December 2020

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

1 reference

12 December 2020

Parkinsonism, Lrrk2 G2019S, and tau neuropathology

1 reference

12 December 2020

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

1 reference

12 December 2020

Autosomal dominant familial Parkinson disease: older onset of age, and good response to levodopa therapy

1 reference

12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

12 December 2020

Parkin disease: a phenotypic study of a large case series

1 reference

12 December 2020

Substantia nigra Marinesco bodies are associated with decreased striatal expression of dopaminergic markers

1 reference

12 December 2020

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/BCR.08.2008.0632

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21686713%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference

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5 February 2020

PubMed publication ID

21686713

1 reference