(Q37438098)

20 August 2017

A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction (English)

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20 August 2017

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10

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20 August 2017

Andreas Puschmann

1

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Zbigniew K Wszolek

9

object named as

Zbigniew K Wszolek

1 reference

20 August 2017

2

Owen A Ross

1 reference

20 August 2017

Carles Vilariño-Güell

3

object named as

Carles Vilariño-Güell

1 reference

20 August 2017

5

Jennifer M Kachergus

1 reference

20 August 2017

11

Håkan Widner

1 reference

20 August 2017

14

Katerina Markopoulou

1 reference

20 August 2017

Sarah J Lincoln

4

1 reference

20 August 2017

Stephanie A Cobb

6

1 reference

20 August 2017

Suzanne G Lindquist

7

1 reference

20 August 2017

Jørgen E Nielsen

8

1 reference

20 August 2017

Danielle van Westen

12

1 reference

20 August 2017

Douglas Hägerström

13

1 reference

20 August 2017

Bruce A Chase

15

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20 August 2017

Karin Nilsson

16

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20 August 2017

Jan Reimer

17

1 reference

20 August 2017

Christer Nilsson

18

1 reference

20 August 2017

25 July 2009

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20 August 2017

6

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Parkinsonism and Related Disorders

inferred from page(s)

published in

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20 August 2017

15

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20 August 2017

9

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20 August 2017

627-632

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Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson's disease. Variability in familial Parkinson's disease

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Concurrence of alpha-synuclein and tau brain pathology in the Contursi kindred

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Diagnostic criteria for Parkinson disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

A large kindred with autosomal dominant Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Criteria for diagnosing Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

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

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

A case of late onset sporadic Parkinson's disease with an A53T mutation in alpha-synuclein.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Fibrillization of alpha-synuclein and tau in familial Parkinson's disease caused by the A53T alpha-synuclein mutation.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Clinical characteristics of the alpha‐synuclein mutation (G209A)‐associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Novel alpha-synuclein-immunoreactive proteins in brain samples from the Contursi kindred, Parkinson's, and Alzheimer's disease.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Alpha synuclein is present in Lewy bodies in sporadic Parkinson's disease.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Validation of a telephone questionnaire for Parkinson's disease.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

The Ala53Thr mutation in the α-synuclein gene in a Korean family with Parkinson disease

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

LRRK2 mutations are a common cause of Parkinson's disease in Spain

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2783246

Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation

3 December 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

Unverricht-Lundborg disease-a misnomer?

1 reference

12 December 2020

10.1016/J.PARKRELDIS.2009.06.007

Identifiers

DOI

1 reference

20 August 2017

1 reference

20 August 2017

1 reference