(Q47753610)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19458969%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

title

LRRK2 and GBA mutations differentially affect the initial presentation of Parkinson disease (English)

1 reference

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28 January 2020

1 reference

1

1 reference

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28 January 2020

Avi Orr-Urtreger

7

1 reference

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28 January 2020

3

A Mirelman

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19458969%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

author name string

A Bar-Shira

2

1 reference

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28 January 2020

T Gurevich

4

1 reference

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28 January 2020

M Kedmi

5

1 reference

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28 January 2020

N Giladi

6

1 reference

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28 January 2020

publication date

21 May 2009

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28 January 2020

1 reference

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28 January 2020

volume

11

1 reference

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28 January 2020

issue

1

1 reference

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28 January 2020

page(s)

121-125

1 reference

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Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

28 January 2020

cites work

1 reference

12 December 2020

Hematologically important mutations: Gaucher disease

1 reference

12 December 2020

A prospective study of familial versus sporadic Parkinson's disease

1 reference

12 December 2020

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

1 reference

12 December 2020

Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease

1 reference

12 December 2020

The biology and pathobiology of LRRK2: implications for Parkinson's disease

1 reference

12 December 2020

Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease

1 reference

12 December 2020

Clinical characteristics of Parkinson's disease among Jewish Ethnic groups in Israel

1 reference

12 December 2020

Emerging pathways in genetic Parkinson's disease: tangles, Lewy bodies and LRRK2.

1 reference

12 December 2020

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

1 reference

12 December 2020

Gaucher and Parkinson diseases: unexpectedly related.

1 reference

12 December 2020

Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy

1 reference

12 December 2020

Defining the Parkinson's disease phenotype: initial symptoms and baseline characteristics in a clinical cohort.

1 reference

12 December 2020

Wild-type LRRK2 but not its mutant attenuates stress-induced cell death via ERK pathway

1 reference

12 December 2020

The Parkinson disease protein leucine-rich repeat kinase 2 transduces death signals via Fas-associated protein with death domain and caspase-8 in a cellular model of neurodegeneration

1 reference

12 December 2020

ER retention and degradation as the molecular basis underlying Gaucher disease heterogeneity

1 reference

12 December 2020

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

1 reference

12 December 2020

Clinical course of patients with idiopathic Parkinson's disease.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset

1 reference

12 December 2020