(Q36817205)

16 August 2017

title

Neuronal intranuclear and neuropil inclusions for pathological assessment of Huntington's disease (English)

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16 August 2017

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2

Raymund Roos

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16 August 2017

Marion Maat-Schieman

1

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16 August 2017

Monique Losekoot

3

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16 August 2017

Josephine Dorsman

4

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16 August 2017

Corrie Welling-Graafland

5

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16 August 2017

Ingrid Hegeman-Kleinn

6

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16 August 2017

Freerk Broeyer

7

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16 August 2017

Martijn Breuning

8

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16 August 2017

Sjoerd van Duinen

9

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16 August 2017

language of work or name

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1 January 2007

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16 August 2017

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16 August 2017

volume

17

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16 August 2017

issue

1

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16 August 2017

page(s)

31-37

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Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype.

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Intranuclear neuronal inclusions in Huntington's disease and dentatorubral and pallidoluysian atrophy: correlation between the density of inclusions and IT15 CAG triplet repeat length

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Stages in the development of Parkinson's disease-related pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Ubiquitin-reactive axons have a widespread distribution and are unrelated to prion protein plaques in Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Genetically confirmed clinical Huntington's disease with no observable cell loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Alpha-synuclein immunoreactivity of huntingtin polyglutamine aggregates in striatum and cortex of Huntington's disease patients and transgenic mouse models

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

From neuronal inclusions to neurodegeneration: neuropathological investigation of a transgenic mouse model of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Neurochemical diversity of dystrophic neurites in the early and late stages of Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Trinucleotide repeats and neurodegenerative disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Neuronal distribution of intranuclear inclusions in Huntington's disease with adult onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Eosinophilic intranuclear inclusions in the hippocampal pyramidal neurons of a patient with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Ubiquitin immunohistochemistry of frontotemporal lobar degeneration differentiates cases with and without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Neuroacanthocytosis misdiagnosed as Huntington's disease: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Huntington disease phenocopy is a familial prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Selective loss of striatal preprotachykinin neurons in a phenocopy of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

The neuropathological features of neuroacanthocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Amyotrophic lateral sclerosis with neuronal intranuclear protein inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Huntington's disease intranuclear inclusions contain truncated, ubiquitinated huntingtin protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Family history and DNA analysis in patients with suspected Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Acanthocytosis and neurological disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Neuronal intranuclear hyaline inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Frequency of hippocampal formation atrophy in normal aging and Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Behavioral Disorder, Dementia, Ataxia, and Rigidity in a Large Family With TATA Box-Binding Protein Mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

Laboratory Guidelines for Huntington Disease Genetic Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.2006.00040.X

10.1111/J.1750-3639.2006.00040.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference