(Q46902452)

English

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins

scientific article published in January 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Parkinson's disease

1 reference

based on heuristic

inferred from title

Ekaterina Rogaeva

10

object named as

Ekaterina Rogaeva

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

Connie Fernández-Cid Marras

3

object named as

Connie Marras

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

9

object named as

Anthony E Lang

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

Lineu Cesar Werneck

6

object named as

Lineu C Werneck

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Danielle Moreno

7

object named as

Danielle Moreno

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

8

object named as

Christine Sato

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Yosuke Wakutani

2

object named as

Yosuke Wakutani

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

5

object named as

Salmo Raskin

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

author name string

Renato P Munhoz

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Helio A Teive

4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

language of work or name

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publication date

1 January 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

23

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

290-294

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

Parkinson's disease. First of two parts

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

Language lateralization in monozygotic twin pairs concordant and discordant for handedness.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

Color and genomic ancestry in Brazilians

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FMDS.21832

21 January 2018

Identifiers

10.1002/MDS.21832

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/17999435

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