(Q74628015)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9619640%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Determinants of cognitive disorders in Autosomal Dominant Cerebellar Ataxia type 1 (English)

1 reference

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12 November 2019

1 reference

1

1 reference

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12 November 2019

author name string

L Chiacchio

2

1 reference

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12 November 2019

D Grossi

3

1 reference

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12 November 2019

A I Pisacreta

4

1 reference

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12 November 2019

O Calabrese

5

1 reference

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12 November 2019

I Castaldo

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9619640%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

G De Michele

7

1 reference

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12 November 2019

A Filla

8

1 reference

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12 November 2019

publication date

1 May 1998

1 reference

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Journal of the Neurological Sciences

12 November 2019

published in

1 reference

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12 November 2019

volume

157

1 reference

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12 November 2019

issue

2

1 reference

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12 November 2019

page(s)

162-167

1 reference

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Memory in patients with cerebellar degeneration.

12 November 2019

cites work

1 reference

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Word length and the structure of short-term memory

7 January 2021

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Neuropsychological changes in olivopontocerebellar atrophy.

7 January 2021

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Friedreich's ataxia in the south of Italy: a clinical and biochemical survey of 23 patients.

7 January 2021

1 reference

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Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

7 January 2021

1 reference

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

7 January 2021

1 reference

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

7 January 2021

1 reference

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7 January 2021

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Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred

7 January 2021

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Cognitive planning deficit in patients with cerebellar atrophy.

7 January 2021

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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'.

7 January 2021

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Spinocerebellar degeneration (SCD): cognitive disturbances.

7 January 2021

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Neuropsychological test performance in patients with dominantly inherited spinocerebellar ataxia: relationship to ataxia severity

7 January 2021

1 reference

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Methodologic considerations in neuropsychologic testing of ataxic patients

7 January 2021

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Metabolic and cognitive changes in hereditary ataxia.

7 January 2021

1 reference

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Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900070-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900070-7

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900070-7

The cerebellum and cognitive functions in humans.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900070-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(98)00070-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9619640%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference