A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity (Q35070572)

6 August 2017

title

A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity (English)

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6 August 2017

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parkinsonian syndrome

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5

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6 August 2017

9

John G Nutt

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6 August 2017

3

James B Leverenz

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6 August 2017

11

Dora Yearout

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6 August 2017

6

Ali Samii

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6 August 2017

1

Parvoneh Poorkaj

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6 August 2017

Wendy H Raskind

2

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6 August 2017

Mark Matsushita

4

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6 August 2017

Sophia Kim

7

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6 August 2017

Nayiry Gazi

8

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6 August 2017

John Wolff

10

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6 August 2017

J Lynne Greenup

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6 August 2017

Ellen J Steinbart

13

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6 August 2017

Thomas D Bird

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6 August 2017

language of work or name

English

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publication date

1 July 2010

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6 August 2017

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6 August 2017

volume

25

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6 August 2017

issue

10

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6 August 2017

page(s)

1409-1417

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LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

6 August 2017

cites work

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Molecular basis of Parkinson's disease

8 July 2018

1 reference

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FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Age at onset in two common neurodegenerative diseases is genetically controlled

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Fragile X syndrome: a model of gene-brain-behavior relationships

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Comprehensive human genetic maps: individual and sex-specific variation in recombination

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Computer-simulation methods in human linkage analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Neuropathological stageing of Alzheimer-related changes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample

8 July 2018

1 reference

Genetic susceptibility to Parkinson's disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.

21 January 2018

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Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

21 January 2018

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Avoiding recomputation in linkage analysis.

21 January 2018

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parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.

21 January 2018

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Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

21 January 2018

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Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.

21 January 2018

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Pallido-pyramidal disease.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3123999

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

27 September 2018

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Consensus recommendations for the postmortem diagnosis of Alzheimer's disease. The National Institute on Aging, and Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer's Disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20629132

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20629132

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular biology. miRNAs in neurodegeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20629132

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/MDS.23085

1 reference

6 August 2017

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6 August 2017

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