Assessment of Whole-Brain White Matter by DTI in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Diffusion Tensor Imaging in Alzheimer’s Disease and Mild Cognitive Impairment

(2014) G. T. Stebbins et al.   BEHAVIOURAL NEUROLOGY

Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series

(2012) E. Prodi et al.   EUROPEAN JOURNAL OF NEUROLOGY

Middle Cerebellar Peduncles and Pontine T2 Hypointensities in ARSACS

(2012) Haruo Shimazaki et al.   JOURNAL OF NEUROIMAGING

Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)

(2012) M. Girard et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Diffusion Tensor Imaging in Huntington’s disease reveals distinct patterns of white matter degeneration associated with motor and cognitive deficits

(2011) India Bohanna et al.   Brain Imaging and Behavior

Thickening of Peripapillar Retinal Fibers for the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

(2011) Jeremy Desserre et al.   CEREBELLUM

Myelinated retinal fibers in autosomal recessive spastic ataxia of Charlevoix-Saguenay

(2011) E. M. Vingolo et al.   EUROPEAN JOURNAL OF NEUROLOGY

New findings in the ataxia of Charlevoix–Saguenay

(2011) José Gazulla et al.   JOURNAL OF NEUROLOGY

Is the ataxia of Charlevoix–Saguenay a developmental disease?

(2011) José Gazulla et al.   MEDICAL HYPOTHESES

Delayed axonal degeneration in slow Wallerian degeneration mutant mice detected using diffusion tensor imaging

(2011) M. Xie et al.   NEUROSCIENCE

Autosomal recessive spastic ataxia of Charlevoix–Saguenay: An overview

(2011) Yosr Bouhlal et al.   PARKINSONISM & RELATED DISORDERS

Noninvasive detection of brainstem and spinal cord axonal degeneration in an amyotrophic lateral sclerosis mouse model

(2010) Joong Hee Kim et al.   NMR IN BIOMEDICINE

Assessment of Brain White Matter Fiber Bundle Atrophy in Patients with Friedreich Ataxia

(2010) Elisabetta Pagani et al.   RADIOLOGY

The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1

(2009) David A. Parfitt et al.   HUMAN MOLECULAR GENETICS

Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management

(2009) M. Anheim et al.   NEUROGENETICS

Diffusion Tensor MR Imaging and Fiber Tractography: Technical Considerations

(2008) P. Mukherjee et al.   AMERICAN JOURNAL OF NEURORADIOLOGY

Longitudinal Investigations on the Anterograde and Retrograde Degeneration in the Pyramidal Tract following Pontine Infarction with Diffusion Tensor Imaging

(2008) Zhijian Liang et al.   CEREBROVASCULAR DISEASES

Retrograde Wallerian degeneration of cranial corticospinal tracts in cervical spinal cord injury patients using diffusion tensor imaging

(2008) Saurabh Guleria et al.   JOURNAL OF NEUROSCIENCE RESEARCH

ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia

(2008) Sascha Vermeer et al.   NEUROGENETICS

Brain white matter tracts degeneration in Friedreich ataxia. An in vivo MRI study using tract-based spatial statistics and voxel-based morphometry

(2008) Riccardo Della Nave et al.   NEUROIMAGE

Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay

(2007) Antonio García et al.   MUSCLE & NERVE