(Q37309837)

English

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

scientific article published on 04 April 2008

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

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

1 reference

Europe PubMed Central

19 August 2017

Parkinson's disease

1 reference

based on heuristic

inferred from title

Dennis W. Dickson

2

1 reference

Europe PubMed Central

19 August 2017

Zbigniew K Wszolek

4

object named as

Z K Wszolek

1 reference

Europe PubMed Central

19 August 2017

author name string

K Markopoulou

1

1 reference

Europe PubMed Central

19 August 2017

R D McComb

3

1 reference

Europe PubMed Central

19 August 2017

L Katechalidou

5

1 reference

Europe PubMed Central

19 August 2017

L Avery

6

1 reference

Europe PubMed Central

19 August 2017

M S Stansbury

7

1 reference

Europe PubMed Central

19 August 2017

B A Chase

8

1 reference

Europe PubMed Central

19 August 2017

publication date

4 April 2008

1 reference

Europe PubMed Central

19 August 2017

Acta Neuropathologica

1 reference

Europe PubMed Central

19 August 2017

116

1 reference

Europe PubMed Central

19 August 2017

1

1 reference

Europe PubMed Central

19 August 2017

25-35

1 reference

Europe PubMed Central

19 August 2017

https://scigraph.springernature.com/pub.10.1007/s00401-008-0372-4

0 references

alpha-Synuclein aggregates interfere with Parkin solubility and distribution: role in the pathogenesis of Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Hippocampal sclerosis dementia differs from hippocampal sclerosis in frontal lobe degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Stanley Fahn Lecture 2005: The staging procedure for the inclusion body pathology associated with sporadic Parkinson's disease reconsidered

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Understanding the molecular causes of Parkinson's disease.

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6 September 2017

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

1 reference

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6 September 2017

Untangling the tau gene association with neurodegenerative disorders.

1 reference

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6 September 2017

Interface between tauopathies and synucleinopathies: A tale of two proteins

1 reference

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6 September 2017

Parkin counteracts symptoms in a Drosophila model of Parkinson's disease

1 reference

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6 September 2017

Parkin and alpha-synuclein: opponent actions in the pathogenesis of Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications

1 reference

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6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Genotype-phenotype correlation: familial Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Colocalization of Tau and Alpha-Synuclein Epitopes in Lewy Bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Higher order arrangement of the eukaryotic nuclear bodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Concurrence of alpha-synuclein and tau brain pathology 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=2728685

6 September 2017

Genetic modifiers of vision and hearing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Argyrophilic grain disease: neuropathology, frequency in a dementia brain bank and lack of relationship with apolipoprotein E.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

Modifier genes in mice and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

26 June 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=2728685

26 June 2018

A neuropathological subset of Alzheimer's disease with concomitant Lewy body disease and spongiform change

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

26 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

26 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

Clinical heterogeneity of alpha-synuclein gene duplication 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=2728685

2 September 2018

A Caenorhabditis elegans Parkin mutant with altered solubility couples alpha-synuclein aggregation to proteotoxic stress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

Complete genomic screen in Parkinson disease: evidence for multiple genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728685

2 September 2018

Staging of argyrophilic grains: an age-associated tauopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

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/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18389263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00401-008-0372-4

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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