(Q50543611)

English

Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease

scientific article published in April 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

Low frequency of Parkin, Tyrosine Hydroxylase, and GTP Cyclohydrolase I gene mutations in a Danish population of early-onset Parkinson's Disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

Parkinson's disease

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based on heuristic

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author name string

J M Hertz

1

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

K Ostergaard

2

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

I Juncker

3

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

S Pedersen

4

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

A Romstad

5

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

L B Møller

6

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

F Güttler

7

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

E Dupont

8

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

publication date

1 April 2006

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

European Journal of Neurology

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

13

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

4

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

385-390

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

Parkinson's disease. First of two parts

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Familial juvenile parkinsonism: clinical and pathologic study in a family

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Parkin disease: a phenotypic study of a large case series

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Lewy bodies and parkinsonism in families with parkin mutations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Complex relationship between Parkin mutations and Parkinson disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Parkin mutations are frequent in patients with isolated early-onset parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Identification and characterization of the human parkin gene promoter

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

How much phenotypic variation can be attributed to parkin genotype?

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2006.01249.X

21 January 2018

Identifiers

10.1111/J.1468-1331.2006.01249.X

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/16643317

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