Autosomal recessive spastic ataxia of Charlevoix-Saguenay

Neurology

Volumn 72, Issue 20, 2009, Pages 1790-

  Van Damme, Philip ^a,b   Demaerel, Philippe ^a   Spileers, Werner ^a   Robberecht, Wim ^a   Belgium, Leuven ^a  

^a UZ Leuven ^*

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; ATAXIA; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX SAGUENAY; CASE REPORT; CEREBELLUM ATROPHY; CEREBELLUM VERMIS; CLINICAL FEATURE; DEMYELINATING NEUROPATHY; DIAGNOSTIC IMAGING; FEMALE; GAIT DISORDER; HUMAN; IMAGE ANALYSIS; NEUROIMAGING; PONS; PRIORITY JOURNAL; SPASTICITY; SYMPTOM; BRAIN; DEGENERATIVE DISEASE; ELECTROMYOGRAPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY; PATHOPHYSIOLOGY; RETINA; SPINOCEREBELLAR DEGENERATION;

ADULT; BRAIN; ELECTROMYOGRAPHY; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; NEURODEGENERATIVE DISEASES; RETINA; SPINOCEREBELLAR ATAXIAS;

EID: 66149097786     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181a60a9a     Document Type: Note

References (2)

1. Martin MH, Bouchard JP, Sylvain M, St-Onge O, Truchon S. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a report of MR imaging in 5 patients. AJNR Am J Neuroradiol 2007:28:1606-1608.
2. Engert JC, Berube P, Mercier J, et al. ARSACS, a spastic ataxia common in northeastern Ouebec, is caused by mutations in a new gene encoding an 11.5-kb ORF. Nat Genet 2000;24