(Q36925651)

17 August 2017

0 references

α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy? (English)

1 reference

17 August 2017

1 reference

4

Patricia Limousin

1 reference

17 August 2017

9

Andrew J Lees

1 reference

17 August 2017

10

John Hardy

1 reference

17 August 2017

8

Niall Quinn

1 reference

17 August 2017

13

Janice L Holton

1 reference

17 August 2017

Aoife P Kiely

1

1 reference

17 August 2017

Yasmine T Asi

2

1 reference

17 August 2017

Eleanna Kara

3

1 reference

17 August 2017

Helen Ling

5

1 reference

17 August 2017

Patrick Lewis

6

1 reference

17 August 2017

Christos Proukakis

7

1 reference

17 August 2017

Tamas Revesz

11

1 reference

17 August 2017

Henry Houlden

12

1 reference

17 August 2017

12 February 2013

1 reference

17 August 2017

Acta Neuropathologica

1 reference

17 August 2017

125

1 reference

17 August 2017

5

1 reference

17 August 2017

753-769

1 reference

Creative Commons Attribution 2.0 Generic

17 August 2017

start time

12 February 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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The neuropathology, pathophysiology and genetics of multiple system atrophy

29 September 2017

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Parkinson's disease and α-synuclein expression

29 September 2017

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Neuropathology underlying clinical variability in patients with synucleinopathies

29 September 2017

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Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?

29 September 2017

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Preparation and characterization of neurotoxic tau oligomers

29 September 2017

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TDP-43 pathology occurs infrequently in multiple system atrophy

29 September 2017

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Synergistic Interactions between Abeta, tau, and alpha-synuclein: acceleration of neuropathology and cognitive decline

29 September 2017

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Tyrosine and serine phosphorylation of alpha-synuclein have opposing effects on neurotoxicity and soluble oligomer formation

29 September 2017

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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy

29 September 2017

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

29 September 2017

1 reference

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SNCA variants are associated with increased risk for multiple system atrophy

29 September 2017

1 reference

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Specificity and regulation of casein kinase-mediated phosphorylation of alpha-synuclein

29 September 2017

1 reference

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

29 September 2017

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Hippocampal sclerosis dementia: a reappraisal

29 September 2017

1 reference

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TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Quantification of alpha-synuclein binding to lipid vesicles using fluorescence correlation spectroscopy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Structure and dynamics of micelle-bound human alpha-synuclein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Mutation E46K increases phospholipid binding and assembly into filaments of human alpha-synuclein

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

29 September 2017

1 reference

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Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications

29 September 2017

1 reference

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The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

29 September 2017

1 reference

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alpha-Synuclein locus triplication causes Parkinson's disease

29 September 2017

1 reference

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Interactions of Amyloidogenic Proteins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Staging of brain pathology related to sporadic Parkinson's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

alpha-Synuclein is phosphorylated in synucleinopathy lesions

29 September 2017

1 reference

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Multiple phosphorylation of alpha-synuclein by protein tyrosine kinase Syk prevents eosin-induced aggregation

29 September 2017

1 reference

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Pathoanatomy of Parkinson's disease

29 September 2017

1 reference

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

29 September 2017

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

29 September 2017

1 reference

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Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Staging of Alzheimer's disease-related neurofibrillary changes

29 September 2017

1 reference

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Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome).

29 September 2017

1 reference

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A large kindred with autosomal dominant Parkinson's disease

29 September 2017

1 reference

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Elucidating the role of C-terminal post-translational modifications using protein semisynthesis strategies: α-synuclein phosphorylation at tyrosine 125.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Hyperphosphorylation and insolubility of alpha-synuclein in transgenic mouse oligodendrocytes

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Nigral and cortical Lewy bodies and dystrophic nigral neurites in Parkinson's disease and cortical Lewy body disease contain alpha-synuclein immunoreactivity

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Familial parkinsonism and dementia with ballooned neurons, argyrophilic neuronal inclusions, atypical neurofibrillary tangles, tau-negative astrocytic fibrillary tangles, and Lewy bodies.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Hippocampal degeneration differentiates diffuse Lewy body disease (DLBD) from Alzheimer's disease: Light and electron microscopic immunocytochemistry of CA2-3 neurites specific to DLBD

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Pale neurites, premature α-synuclein aggregates with centripetal extension from axon collaterals.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

SNCA variants and multiple system atrophy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

First appraisal of brain pathology owing to A30P mutant alpha-synuclein

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Reply to: SNCA variants are associated with increased risk of multiple system atrophy

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

alpha-Synuclein promotes the recruitment of tau to protein inclusions in oligodendroglial cells: effects of oxidative and proteolytic stress

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Proposed neuropathological criteria for the post mortem diagnosis of multiple system atrophy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Synucleinopathy with features of both multiple system atrophy and dementia with Lewy bodies.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Hippocampal neuron and glial cell numbers in Parkinson's disease--a stereological study

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Multiple system atrophy (MSA): topographic distribution of the alpha-synuclein-associated pathological changes.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Alpha B-crystallin is a major component of glial cytoplasmic inclusions in multiple system atrophy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Dementia with Lewy bodies: reclassification of pathological subtypes and boundary with Parkinson's disease or Alzheimer's disease.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

More than just two peas in a pod: common amyloidogenic properties of tau and alpha-synuclein in neurodegenerative diseases

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Morphogenesis of Lewy bodies: dissimilar incorporation of alpha-synuclein, ubiquitin, and p62.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Conformational properties of alpha-synuclein in its free and lipid-associated states

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

The distribution and dynamic density of oligodendroglial cytoplasmic inclusions (GCIs) in multiple system atrophy: a correlation between the density of GCIs and the degree of involvement of striatonigral and olivopontocerebellar systems.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Neuronal inclusions in the dentate fascia in patients with multiple system atrophy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Immunoreactivity profile of hippocampal CA2/3 neurites in diffuse Lewy body disease

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3681325

Tonicity-dependent induction of Sgk1 expression has a potential role in dehydration-induced natriuresis in rodents.

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00401-013-1096-7

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00401-013-1096-7

Distinctive neuropathology revealed by α-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00401-013-1096-7

21 January 2018

1 reference

12 December 2020

Asymmetrical temporal lobe atrophy with massive neuronal inclusions in multiple system atrophy

1 reference

12 December 2020

Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease

1 reference

12 December 2020

Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementia

1 reference

12 December 2020

alpha-Synuclein pathology in the neostriatum in Parkinson's disease

1 reference

12 December 2020

Three-layered structure shared between Lewy bodies and lewy neurites-three-dimensional reconstruction of triple-labeled sections

1 reference

12 December 2020

NACP/alpha-synuclein-positive filamentous inclusions in astrocytes and oligodendrocytes of Parkinson's disease brains

1 reference

12 December 2020

1 reference

12 December 2020

alpha-Synuclein membrane interactions and lipid specificity

1 reference

12 December 2020

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease

1 reference

12 December 2020

Young onset Parkinson's disease

1 reference

12 December 2020

10.1007/S00401-013-1096-7

Identifiers

DOI

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

23404372

1 reference