The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study. (Q35215614)

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10 February 2020

title

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study (English)

1 reference

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spinocerebellar ataxia type 1

10 February 2020

main subject

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12

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10 February 2020

5

M G Sweeney

1 reference

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10 February 2020

author name string

H Jacobi

1

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10 February 2020

P Bauer

2

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10 February 2020

P Giunti

3

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10 February 2020

R Labrum

4

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10 February 2020

P Charles

6

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10 February 2020

A Dürr

7

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10 February 2020

C Marelli

8

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10 February 2020

C Globas

9

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10 February 2020

C Linnemann

10

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10 February 2020

L Schöls

11

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10 February 2020

R Rola

13

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10 February 2020

E Zdzienicka

14

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10 February 2020

T Schmitz-Hübsch

15

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10 February 2020

R Fancellu

16

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10 February 2020

C Mariotti

17

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10 February 2020

C Tomasello

18

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10 February 2020

L Baliko

19

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10 February 2020

B Melegh

20

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A Filla

21

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10 February 2020

C Rinaldi

22

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B P van de Warrenburg

23

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C C P Verstappen

24

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S Szymanski

25

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10 February 2020

J Berciano

26

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10 February 2020

J Infante

27

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10 February 2020

D Timmann

28

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10 February 2020

S Boesch

29

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10 February 2020

S Hering

30

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10 February 2020

C Depondt

31

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M Pandolfo

32

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10 February 2020

J-S Kang

33

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S Ratzka

34

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10 February 2020

J Schulz

35

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10 February 2020

S Tezenas du Montcel

36

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10 February 2020

T Klockgether

37

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10 February 2020

language of work or name

English

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publication date

10 August 2011

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10 February 2020

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10 February 2020

volume

77

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10 February 2020

page(s)

1035-1041

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10 February 2020

issue

11

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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease

10 February 2020

cites work

1 reference

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Trinucleotide Repeat Disorders

13 July 2018

1 reference

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Scale for the assessment and rating of ataxia: development of a new clinical scale

13 July 2018

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13 July 2018

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Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

13 July 2018

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13 July 2018

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SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene

13 July 2018

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13 July 2018

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13 July 2018

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Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

13 July 2018

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Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

13 July 2018

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

13 July 2018

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Correlation between CAG repeat length and clinical features in Machado-Joseph disease

13 July 2018

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13 July 2018

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13 July 2018

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12 December 2020

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12 December 2020

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12 December 2020

10.1212/WNL.0B013E31822E7CA0

Identifiers

DOI

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10 February 2020

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10 February 2020

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