Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings. (Q49131319)

18 February 2018

title

Spinocerebellar ataxia types 1, 2, 3 and 6: the clinical spectrum of ataxia and morphometric brainstem and cerebellar findings. (English)

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18 February 2018

main subject

spinocerebellar ataxia

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Sophie Tezenas du Montcel

inferred from title

author

30

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Jörg B. Schulz

32

Jörg B Schulz

1 reference

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Ludger Schöls

22

Ludger Schöls

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Thomas Klockgether

33

Thomas Klockgether

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Tanja Schmitz-Hübsch

6

Tanja Schmitz-Hübsch

1 reference

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Dagmar Timmann

17

Dagmar Timmann

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Chantal Depondt

21

Chantal Depondt

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Sylvia Boesch

18

Sylvia Boesch

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Roberto Fancellu

19

Roberto Fancellu

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Christoph Globas

4

Christoph Globas

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Jun-Suk Kang

24

Jun-Suk Kang

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Berry Kremer

26

Berry Kremer

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Rafał Rola

20

Rafal Rola

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Sandra Szymanski

13

Sandra Szymanski

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Bart van de Warrenburg

15

Bart P C van de Warrenburg

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Elszbieta Zdzienicka

23

Elzbieta Zdzienicka

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Alexandra Durr

16

Alexandra Dürr

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Susanne Ratzka

25

Susanne Ratzka

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Massimo Pandolfo

29

Massimo Pandolfo

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Heike Jacobi

1

Heike Jacobi

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Till-Karsten Hauser

2

Till-Karsten Hauser

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Johannes Borkert

31

Johannes Borkert

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author name string

Paola Giunti

3

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Peter Bauer

5

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László Baliko

7

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Alessandro Filla

8

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Caterina Mariotti

9

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Maria Rakowicz

10

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Perine Charles

11

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Pascale Ribai

12

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Jon Infante

14

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Dennis A Stephenson

27

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Béla Melegh

28

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publication date

1 March 2012

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18 February 2018

published in

The Cerebellum

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18 February 2018

volume

11

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18 February 2018

issue

1

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18 February 2018

page(s)

155-166

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18 February 2018

https://scigraph.springernature.com/pub.10.1007/s12311-011-0292-z

exact match

0 references

cites work

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Trinucleotide Repeat Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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/10.1007%2FS12311-011-0292-Z

Spinocerebellar ataxia type 2. Genotype and phenotype in German kindreds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Reliability and validity of the scale for the assessment and rating of ataxia: a study in 64 ataxia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Impairments of prehension kinematics and grasping forces in patients with cerebellar degeneration and the relationship to cerebellar atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

A new semiautomated, three-dimensional technique allowing precise quantification of total and regional cerebellar volume using MRI.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

An optimized method for estimating intracranial volume from magnetic resonance images.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Oculomotor phenotypes in autosomal dominant ataxias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Relative atrophy of the flocculus and ocular motor dysfunction in SCA2 and SCA6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Clinical manifestation of focal cerebellar disease as related to the organization of neural pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12311-011-0292-Z

Gait disturbances in patients with pontine medial tegmental lesions: clinical characteristics and gait analysis

21 January 2018

1 reference

12 December 2020

The thalamic ataxia syndrome

1 reference

12 December 2020

Spinocerebellar ataxia type 6: Systematic patho-anatomical study reveals different phylogenetically defined regions of the cerebellum and neural pathways undergo different evolutions of the degenerative process.

1 reference

12 December 2020

Compartmentalized cerebellar functions upon the stabilization of body posture.

1 reference

12 December 2020

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

1 reference

12 December 2020

Topodiagnostic implications of hemiataxia: an MRI-based brainstem mapping analysis

1 reference

12 December 2020

The spinocerebellar ataxias

1 reference

12 December 2020

Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion

1 reference

12 December 2020

Spinocerebellar ataxia types 1, 2, 3, and 6: Disease severity and nonataxia symptoms

1 reference

12 December 2020

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3

1 reference

12 December 2020

10.1007/S12311-011-0292-Z

Identifiers

DOI

1 reference

18 February 2018

Dimensions Publication ID

1001516357

0 references

Fatcat ID

release_f36kgm22rbhpvnmkkwnabhwp4e

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/f36kgm22rbhpvnmkkwnabhwp4e

24 November 2022

mapped directly with Wikidata item

PubMed ID

21701895

1 reference

18 February 2018