(Q35542418)

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Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient

scientific article published on October 1, 2003

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scholarly article

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Europe PubMed Central

8 August 2017

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Europe PubMed Central

Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient (English)

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Europe PubMed Central

8 August 2017

spinocerebellar ataxia type 2

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based on heuristic

inferred from title

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10.1046/J.1365-2990.2003.00504.X

https://api.crossref.org/works/10.1046/J.1365-2990.2003.00504.X

13 March 2024

author name string

de Vos RA

6

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8 August 2017

U. Rüb

1

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13 March 2024

C. Schultz

2

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13 March 2024

K. Del Tredici

3

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13 March 2024

K. Gierga

4

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G. Reifenberger

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R. A I. de Vos

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C. Seifried

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H. Braak

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G. Auburger

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publication date

1 October 2003

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full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2990.2003.00504.x

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10.1046/J.1365-2990.2003.00504.X

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13 March 2024

https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2990.2003.00504.x

1 reference

10.1046/J.1365-2990.2003.00504.X

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13 March 2024

Neuropathology and Applied Neurobiology

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Europe PubMed Central

8 August 2017

29

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Europe PubMed Central

8 August 2017

5

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Europe PubMed Central

8 August 2017

418-433

1 reference

Europe PubMed Central

8 August 2017

Abnormalities of parietal and prerolandic somatosensory evoked potentials in Huntington's disease

1 reference

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Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.

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Neuropathological stageing of Alzheimer-related changes

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Involvement of precerebellar nuclei in multiple system atrophy.

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Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.

1 reference

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Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families

1 reference

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Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.

1 reference

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The spinocerebellar ataxias

1 reference

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Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions.

1 reference

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Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2.

1 reference

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Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n

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Clinicopathological study of the peripheral nervous system in Machado-Joseph disease.

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Genes involved in hereditary ataxias.

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The molecular biology of the autosomal-dominant cerebellar ataxias

1 reference

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Multiarchitectonic and stereotactic atlas of the human thalamus.

1 reference

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SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

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Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient.

1 reference

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21 January 2018

Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease).

1 reference

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Spinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleus.

1 reference

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21 January 2018

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

1 reference

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Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

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Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.

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Cyto-, myelo-, and receptor architectonics of the human parietal cortex.

1 reference

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21 January 2018

1 reference

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Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1

1 reference

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21 January 2018

The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia

1 reference

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21 January 2018

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2990.2003.00504.X

21 January 2018

A new parcellation of the human thalamus on the basis of histochemical staining

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A rapid myelin stain for frozen sections: modification of the Heidenhain procedure

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Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12

1 reference

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21 January 2018

Spinal Cord: Cytoarchitectural, Dendroarchitectural, and Myeloarchitectural Organization

1 reference

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21 January 2018

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds

1 reference

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Sexual dimorphism of the anterior commissure and massa intermedia of the human brain

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Sensory involvement in spinal-bulbar muscular atrophy (Kennedy's disease).

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Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

11

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Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies)

15

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The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia

18

1 reference

10.1046/J.1365-2990.2003.00504.X

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Cortical and striatal neurone number in Huntington's disease

25

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Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

32

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Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of Huntington's disease

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Swallowing, ingestion and dysphagia: a reappraisal

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Primary sensory neurons in X-linked recessive bulbospinal neuropathy: histopathology and androgen receptor gene expression

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Toward an understanding of polyglutamine neurodegeneration

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Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological study.

56

1 reference

10.1046/J.1365-2990.2003.00504.X

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Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

57

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The neuropathology of CAG repeat diseases: review and update of genetic and molecular features

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Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

64

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Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients

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13 March 2024

Identifiers

10.1046/J.1365-2990.2003.00504.X

1 reference

Europe PubMed Central

8 August 2017

1 reference

Europe PubMed Central

8 August 2017

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