(Q50746812)

18 March 2018

title

Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. (English)

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18 March 2018

spinocerebellar ataxia type 4

main subject

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Y Hellenbroich

1

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18 March 2018

K Gierga

2

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18 March 2018

E Reusche

3

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18 March 2018

E Schwinger

4

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18 March 2018

T Deller

5

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18 March 2018

R A I de Vos

6

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18 March 2018

C Zühlke

7

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18 March 2018

U Rüb

8

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18 March 2018

publication date

19 December 2005

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18 March 2018

Journal of Neural Transmission

published in

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18 March 2018

volume

113

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18 March 2018

issue

7

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18 March 2018

page(s)

829-843

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18 March 2018

https://scigraph.springernature.com/pub.10.1007/s00702-005-0362-9

exact match

0 references

cites work

Hereditary ataxia with sensory neuronopathy: Biemond's ataxia.

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Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3.

21 January 2018

1 reference

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https://api.crossref.org/works/10.1007%2FS00702-005-0362-9

Isolation and characterization of novel CAG repeat containing genes expressed in human brain

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00702-005-0362-9

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

21 January 2018

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12 December 2020

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12 December 2020

Functional anatomy of auditory brainstem nuclei: application to the anatomical basis of brainstem auditory evoked potentials.

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12 December 2020

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

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Refinement of the spinocerebellar ataxia type 4 locus in a large German family and exclusion of CAG repeat expansions in this region

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

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The role of the cerebellum in voluntary eye movements

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The spinocerebellar ataxias

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12 December 2020

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1

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12 December 2020

Contribution from crossed and uncrossed brainstem structures to the brainstem auditory evoked potentials: a study in humans

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12 December 2020

Ataxia and hereditary disorders

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12 December 2020

Spinocerebellar ataxia type 4. Investigation of 34 candidate genes.

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

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Frontal cortical control of smooth-pursuit

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The molecular biology of the autosomal-dominant cerebellar ataxias

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Autosomal dominant spinocerebellar degenerations. Clinical, pathological, and genetic correlations.

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

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Antibody-based detection of CAG repeat expansion containing genes

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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

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12 December 2020

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

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12 December 2020

Polyethylene glycol embedding: a technique compatible with immunocytochemistry, enzyme histochemistry, histofluorescence and intracellular staining.

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12 December 2020

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance

1 reference

12 December 2020

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease).

1 reference

12 December 2020

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

1 reference

12 December 2020

Involvement of precerebellar nuclei in multiple system atrophy

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12 December 2020

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

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12 December 2020

Three-dimensional MRI atlas of the human cerebellum in proportional stereotaxic space

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12 December 2020

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

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12 December 2020

10.1007/S00702-005-0362-9

Identifiers

DOI

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18 March 2018

1 reference

18 March 2018