(Q44125029)

30 November 2017

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations (English)

1 reference

30 November 2017

1 reference

parkinsonian syndrome

1 reference

1

1 reference

30 November 2017

5

1 reference

30 November 2017

8

1 reference

30 November 2017

12

1 reference

30 November 2017

10

John Hardy

1 reference

30 November 2017

9

Katrina Gwinn-Hardy

1 reference

30 November 2017

7

Jennifer Hussey

1 reference

30 November 2017

6

Chun-Hwei Tai

1 reference

30 November 2017

13

Sarah Lincoln

1 reference

30 November 2017

Din-E Shan

2

1 reference

30 November 2017

Chen-Ming Sun

series ordinal

3

1 reference

30 November 2017

Ren-Shyan Liu

series ordinal

4

1 reference

30 November 2017

Judy Chen

series ordinal

11

1 reference

30 November 2017

language of work or name

English

0 references

publication date

1 July 2002

1 reference

30 November 2017

1 reference

30 November 2017

17

1 reference

30 November 2017

670-675

1 reference

30 November 2017

4

1 reference

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

30 November 2017

1 reference

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

21 January 2018

1 reference

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

21 January 2018

1 reference

Association between early-onset Parkinson's disease and mutations in the parkin gene

21 January 2018

1 reference

Lewy bodies and parkinsonism in families with parkin mutations

21 January 2018

1 reference

21 January 2018

1 reference

Diagnostic criteria for essential tremor: a population perspective.

21 January 2018

1 reference

Diagnostic criteria for Parkinson disease

21 January 2018

1 reference

An Inventory for Measuring Depression

21 January 2018

1 reference

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family

21 January 2018

1 reference

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

21 January 2018

1 reference

Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family

21 January 2018

1 reference

Differing patterns of striatal 18F-dopa uptake in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.10184

1 reference

release_z6voroldebbyhma6j666xynb3q

30 November 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/z6voroldebbyhma6j666xynb3q

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference