Friedreich ataxia: The clinical picture

Journal of Neurology

Volumn 256, Issue SUPPL. 1, 2009, Pages 3-8

  Pandolfo, Massimo ^a  

^a ERASME HOSPITAL   (Belgium)

Author keywords

Dysarthria; Frataxin gene mutation; Gait instability; Gene silencing; Hypertrophic cardiomyopathy; Inherited ataxia; Muscle weakness; Pyramidal tract degeneration; Sensory loss

Indexed keywords

FRATAXIN;

CLINICAL FEATURE; DISABILITY; DISEASE COURSE; DYSARTHRIA; ELECTRONEUROLOGY; EVOKED RESPONSE; FOOT MALFORMATION; FRIEDREICH ATAXIA; GENE MUTATION; GENE SILENCING; HYPERTROPHIC CARDIOMYOPATHY; INTRON; KYPHOSCOLIOSIS; MUSCLE HYPERTROPHY; MUSCLE WEAKNESS; NEUROLOGIC DISEASE; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; REVIEW; SENSORY DYSFUNCTION; SENSORY NEUROPATHY; SPINAL CORD ATROPHY; SPINAL CORD DORSAL HORN; SPINAL GANGLION; TRINUCLEOTIDE REPEAT;

ANIMALS; FRIEDREICH ATAXIA; HUMANS; IRON-BINDING PROTEINS; MUTATION; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 62549117369     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-009-1002-3     Document Type: Review

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