(Q77348728)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10210910%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

title

Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset (English)

1 reference

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4 December 2019

10

1 reference

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4 December 2019

author name string

S Giuffrida

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10210910%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

S Lanza

2

1 reference

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4 December 2019

D A Restivo

3

1 reference

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4 December 2019

R Saponara

4

1 reference

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4 December 2019

S C Valvo

5

1 reference

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4 December 2019

F Le Pira

6

1 reference

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4 December 2019

A Trovato Salinaro

7

1 reference

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4 December 2019

F Spinella

8

1 reference

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4 December 2019

A Nicoletti

9

1 reference

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4 December 2019

publication date

1 May 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10210910%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Neurology

4 December 2019

published in

1 reference

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4 December 2019

volume

6

1 reference

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4 December 2019

issue

3

1 reference

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4 December 2019

page(s)

301-307

1 reference

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Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

4 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Rapid touchdown PCR assay for the molecular diagnosis of spinocerebellar ataxia type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

HIV or zidovudine myopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Machado-Joseph disease and SCA3: the genotype meets the phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

SCA2 trinucleotide expansion in German SCA patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1999.630301.X

10.1046/J.1468-1331.1999.630301.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10210910%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference