(Q28266674)

9 April 2017

1 reference

5

Z. K. Wszolek

1 reference

9 April 2017

4

M J Farrer

0 references

Matthew J. Farrer

4

object named as

M. J. Farrer

1 reference

9 April 2017

author name string

N R Whaley

1

0 references

R J Uitti

2

0 references

D W Dickson

3

0 references

Z K Wszolek

5

0 references

N. R. Whaley

1

1 reference

9 April 2017

R. J. Uitti

2

1 reference

9 April 2017

D. W. Dickson

3

1 reference

Journal of neural transmission. Supplementum

9 April 2017

language of work or name

English

0 references

publication date

2006

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published in

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Journal of Neural Transmission. Supplementa

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issue

70

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page(s)

221-9

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221-229

1 reference

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

9 April 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

Molecular pathogenesis of Parkinson disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

Familial Parkinson's disease: clinical and genetic analysis of four Basque families.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

Western Nebraska family (family D) with autosomal dominant parkinsonism

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34

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

31 March 2020

1 reference

https://api.crossref.org/works/10.1007%2F978-3-211-45295-0_34