4.7 Article

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Brain pathology of spinocerebellar ataxias

Kay Seidel et al.

ACTA NEUROPATHOLOGICA (2012)

Article Clinical Neurology

Neocortical Atrophy in Machado-Joseph Disease: A Longitudinal Neuroimaging Study

Anelyssa D'Abreu et al.

JOURNAL OF NEUROIMAGING (2012)

Article Clinical Neurology

Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights

U. Rueb et al.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2012)

Article Clinical Neurology

Thalamic Volume and Dystonia in Machado-Joseph Disease

Anelyssa D'Abreu et al.

JOURNAL OF NEUROIMAGING (2011)

Review Clinical Neurology

Movement Disorders in Spinocerebellar Ataxias

Judith van Gaalen et al.

MOVEMENT DISORDERS (2011)

Article Clinical Neurology

Gray matter volume deficits in spinocerebellar ataxia: An optimized voxel based morphometric study

Gaurav Goel et al.

PARKINSONISM & RELATED DISORDERS (2011)

Article Clinical Neurology

The wide clinical spectrum and nigrostriatal dopaminergic damage in spinocerebellar ataxia type 6

Jong-Min Kim et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2010)

Review Clinical Neurology

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

Alexandra Durr

LANCET NEUROLOGY (2010)

Article Geriatrics & Gerontology

Longitudinal MRI atrophy biomarkers: Relationship to conversion in the ADNI cohort

Shannon L. Risacher et al.

NEUROBIOLOGY OF AGING (2010)

Article Clinical Neurology

Responsiveness of different rating instruments in spinocerebellar ataxia patients

T. Schmitz-Huebsch et al.

NEUROLOGY (2010)

Article Clinical Neurology

The Spinocerebellar Ataxias

Henry L. Paulson

JOURNAL OF NEURO-OPHTHALMOLOGY (2009)

Article Neurosciences

A probabilistic MR atlas of the human cerebellum

Joern Diedrichsen et al.

NEUROIMAGE (2009)

Article Clinical Neurology

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites

K. Gierga et al.

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2009)

Article Clinical Neurology

Brain structural damage in spinocerebellar ataxia type 1 - A VBM study

Andrea Ginestroni et al.

JOURNAL OF NEUROLOGY (2008)

Article Clinical Neurology

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

T. Schmitz-Huebsch et al.

NEUROLOGY (2008)

Article Neurosciences

A spatially unbiased atlas template of the human cerebellum

Jorn Diedrichsen

NEUROIMAGE (2006)

Article Clinical Neurology

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

T. Schmitz-Huebsch et al.

NEUROLOGY (2006)

Article Clinical Neurology

Visualization and quantification of disease progression in multiple system atrophy

Till-Karsten Hauser et al.

MOVEMENT DISORDERS (2006)

Article Radiology, Nuclear Medicine & Medical Imaging

Radiological characterization of spinocerebellar ataxia type 6

D Butteriss et al.

BRITISH JOURNAL OF RADIOLOGY (2005)

Article Neurosciences

Unified segmentation

J Ashburner et al.

NEUROIMAGE (2005)

Article Clinical Neurology

Metabolic characterization of spinocerebellar ataxia type 6

BW Soong et al.

ARCHIVES OF NEUROLOGY (2001)