(Q35462051)

English

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

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scholarly article

1 reference

Europe PubMed Central

8 August 2017

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

1 reference

Europe PubMed Central

8 August 2017

Parkinson's disease

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Papapetropoulos S

1

1 reference

Europe PubMed Central

8 August 2017

Paschalis C

2

1 reference

Europe PubMed Central

8 August 2017

Athanassiadou A

3

1 reference

Europe PubMed Central

8 August 2017

Papadimitriou A

4

1 reference

Europe PubMed Central

8 August 2017

Ellul J

5

1 reference

Europe PubMed Central

8 August 2017

Polymeropoulos MH

6

1 reference

Europe PubMed Central

8 August 2017

Papapetropoulos T

7

1 reference

Europe PubMed Central

8 August 2017

language of work or name

0 references

publication date

1 May 2001

1 reference

Europe PubMed Central

8 August 2017

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

Europe PubMed Central

8 August 2017

70

1 reference

Europe PubMed Central

8 August 2017

5

1 reference

Europe PubMed Central

8 August 2017

662-665

1 reference

Europe PubMed Central

8 August 2017

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

Absence of mutations in the coding region of the alpha-synuclein gene in pathologically proven Parkinson's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

Parkinsonism: onset, progression, and mortality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

A large kindred with autosomal dominant Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

27 July 2018

Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

26 September 2018

Lack of mutation G209A in the alpha-synuclein gene in French patients with familial and sporadic Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

26 September 2018

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1737360

26 September 2018

A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced expression of the G209A alpha-synuclein allele in familial Parkinsonism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the alpha-synuclein G209A mutation in familial Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure to find the alpha-synuclein gene missense mutation (G209A) in 100 patients with younger onset Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G209A mutation in the alpha-synuclein gene is rare and not associated with sporadic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The G209A mutation in the alpha-synuclein gene is not detected in familial cases of Parkinson disease in non-Greek and/or Italian populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No mutation of G209A in the alpha-synuclein gene in sporadic Parkinson's disease among Taiwan Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/11309462

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.70.5.662

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

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0 references

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