(Q73589452)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Paraoxonase 1 Met--Leu 54 polymorphism is associated with Parkinson's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

S N Akhmedova

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

A K Yakimovsky

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

E I Schwartz

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 March 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

Journal of the Neurological Sciences

5 November 2019

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

184

1 reference

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5 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

179-182

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

Parkinson disease in twins: an etiologic study

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Paraquat elicited neurobehavioral syndrome caused by dopaminergic neuron loss.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

7 January 2021

Human serum paraoxonase

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

The molecular basis of the human serum paraoxonase activity polymorphism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Effect of the molecular polymorphisms of human paraoxonase (PON1) on the rate of hydrolysis of paraoxon

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Gln --> Arg 191 polymorphism of paraoxonase and Parkinson's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Paraoxonase polymorphism Met-Leu54 is associated with modified serum concentrations of the enzyme. A possible link between the paraoxonase gene and increased risk of cardiovascular disease in diabetes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Parkinsonism: onset, progression, and mortality

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Structural organization of the human PON1 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

The role of paraoxonase (PON1) in the detoxication of organophosphates and its human polymorphism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Paraoxonase PON1 polymorphism leu-Met54 is associated with carotid atherosclerosis: results of the Austrian Stroke Prevention Study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900439-7

10.1016/S0022-510X(01)00439-7

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11239953%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference