(Q38470590)

English

Machado-Joseph disease of Azorean ancestry in Brazil: the Catarina kindred. Neurological, neuroimaging, psychiatric and neuropsychological findings in the largest known family, the "Catarina" kindred

scientific article published on March 1993

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Machado-Joseph disease of Azorean ancestry in Brazil: the Catarina kindred. Neurological, neuroimaging, psychiatric and neuropsychological findings in the largest known family, the "Catarina" kindred (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

0 references

0 references

neuropsychology

1 reference

based on heuristic

inferred from title

Machado-Joseph disease

1 reference

based on heuristic

inferred from title

author name string

Radvany J

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Camargo CH

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Costa ZM

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Fonseca NC

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Nascimento ED

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

1 March 1993

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Arquivos de Neuro-Psiquiatria

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

51

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

21-30

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1)

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Electro-oculographic findings in Machado-Joseph disease.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Familial cerebro-macular degeneration and ataxia

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

A New Depression Scale Designed to be Sensitive to Change

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Machado disease: A hereditary ataxia in Portuguese emigrants to Massachusetts

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Azorean disease of the nervous system

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Autosomal dominant striatonigral degeneration. A clinical, pathologic, and biochemical study of a new genetic disorder

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X1993000100004

21 January 2018

Identifiers

10.1590/S0004-282X1993000100004

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

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