(Q48376525)

11 February 2018

title

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17. (English)

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11 February 2018

main subject

spinocerebellar ataxia

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1

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11 February 2018

Christian Gaser

4

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11 February 2018

Uwe Walter

object named as

Uwe Walter

6

0 references

Christine Klein

11

object named as

Christine Klein

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11 February 2018

2

Rebekka Lencer

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11 February 2018

Ferdinand Binkofski

object named as

Ferdinand Binkofski

13

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author name string

Johannes M Hagenah

3

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11 February 2018

Vera Tadic

5

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11 February 2018

Alexander Wolters

7

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11 February 2018

Susanne Steinlechner

8

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11 February 2018

Christine Zühlke

9

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11 February 2018

Katja Brockmann

10

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11 February 2018

Arndt Rolfs

12

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11 February 2018

publication date

1 June 2010

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11 February 2018

published in

The Cerebellum

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11 February 2018

volume

9

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11 February 2018

issue

2

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11 February 2018

page(s)

210-217

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11 February 2018

Basal ganglia involvement of a patient with SCA 17--a new form of autosomal dominant spinocerebellar ataxia

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12311-009-0150-4

Intergenerational instability and marked anticipation in SCA-17

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12311-009-0150-4

Differential limbic--cortical correlates of sadness and anxiety in healthy subjects: implications for affective disorders.

21 January 2018

1 reference

12 December 2020

Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions

1 reference

12 December 2020

Reduced hippocampal volume correlates with executive dysfunctioning in major depression.

1 reference

12 December 2020

Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers

1 reference

12 December 2020

Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia

1 reference

12 December 2020

Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.

1 reference

12 December 2020

Cerebellar cognitive affective syndrome.

1 reference

12 December 2020

A voxel-based morphometric study of ageing in 465 normal adult human brains

1 reference

12 December 2020

An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets

1 reference

12 December 2020

Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes

1 reference

12 December 2020

The precuneus: a review of its functional anatomy and behavioural correlates

1 reference

12 December 2020

Human anterior cingulate cortex neurons encode cognitive and emotional demands.

1 reference

12 December 2020

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

1 reference

12 December 2020

Putamen dopamine transporter and glucose metabolism are reduced in SCA17.

1 reference

12 December 2020

How do we modulate our emotions? Parametric fMRI reveals cortical midline structures as regions specifically involved in the processing of emotional valences.

1 reference

12 December 2020

Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging

1 reference

12 December 2020

Focal dystonia as a presenting sign of spinocerebellar ataxia 17.

1 reference

12 December 2020

Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6 : a voxel-based FDG-positron emission tomography analysis

1 reference

12 December 2020

Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17).

1 reference

12 December 2020

The SCA17 phenotype can include features of MSA-C, PSP and cognitive impairment

1 reference

12 December 2020

Basal ganglia and cerebellar loops: motor and cognitive circuits

1 reference

12 December 2020

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.

1 reference

12 December 2020

Neuroimaging in Alzheimer disease: an evidence-based review

1 reference

12 December 2020

Nonlinear spatial normalization using basis functions

1 reference

12 December 2020

SCA17 homozygote showing Huntington's disease-like phenotype.

1 reference

12 December 2020

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

1 reference

12 December 2020

Psychopathology in patients with degenerative cerebellar diseases: a comparison to Huntington's disease.

1 reference

12 December 2020

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

1 reference

12 December 2020

Possible mechanisms for atrophy of the human hippocampus

1 reference

12 December 2020

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

1 reference

12 December 2020

Mutation at the SCA17 locus is not a common cause of parkinsonism

1 reference

12 December 2020

Is hippocampal atrophy a future drug target?

1 reference

12 December 2020

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

1 reference

12 December 2020

World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects

1 reference

12 December 2020

10.1007/S12311-009-0150-4

Identifiers

DOI

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11 February 2018

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11 February 2018