(Q61588546)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7839819%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family (English)

1 reference

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27 October 2019

1 reference

9

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27 October 2019

author name string

J J Martin

1

1 reference

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27 October 2019

N Van Regemorter

2

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27 October 2019

L Krols

3

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27 October 2019

J M Brucher

4

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27 October 2019

T de Barsy

5

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27 October 2019

H Szliwowski

6

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27 October 2019

P Evrard

7

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27 October 2019

C Ceuterick

8

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27 October 2019

H Smet-Dieleman

10

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27 October 2019

publication date

1 January 1994

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27 October 2019

published in

Acta Neuropathologica

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27 October 2019

volume

88

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27 October 2019

issue

4

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27 October 2019

page(s)

277-286

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https://scigraph.springernature.com/pub.10.1007/bf00310370

27 October 2019

exact match

0 references

cites work

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population

1 reference

12 December 2020

Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family

1 reference

12 December 2020

Atrophic maculopathy associated with hereditary ataxia

1 reference

12 December 2020

Anatomy of the thalamus and its pathology in degenerative diseases designated as abiotrophic

1 reference

12 December 2020

Adult hereditary cerebelloretinal degeneration

1 reference

12 December 2020

Hereditary multisystemic degeneration with unusual combination of cerebellipetal, dentato-rubral, and nigro-subthalamo-pallidal degenerations.

1 reference

12 December 2020

Machado-Joseph-Azorean disease. A ten-year study.

1 reference

12 December 2020

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

12 December 2020

A 17th-century founder gives rise to a large north American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6

1 reference

12 December 2020

Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis

1 reference

12 December 2020

Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.

1 reference

12 December 2020

Electroretinographic changes in a case of spino-cerebellar degeneration (SCD)

1 reference

12 December 2020

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

12 December 2020

Familial cerebro-macular degeneration and ataxia

1 reference

12 December 2020

Dentatorubropallidoluysian degeneration: clinical, neuro-ophthalmologic, biochemical, and pathologic studies on autosomal dominant form.

1 reference

12 December 2020

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1 reference

12 December 2020

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

1 reference

12 December 2020

Joseph's disease: clinical and pathological studies in a Japanese family

1 reference

12 December 2020

Dégénérescence systématisée optico-cochléo-dentelée

1 reference

12 December 2020

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study

1 reference

12 December 2020

Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3

1 reference

12 December 2020

Retinal degeneration in hereditary ataxia

1 reference

12 December 2020

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

12 December 2020

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

1 reference

12 December 2020

Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

1 reference

12 December 2020

Linkage studies in spinocerebellar ataxia (SCA)

1 reference

12 December 2020

Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxia

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00310370

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7839819%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference