Share
Other content recommended for you
- Hereditary spastic paraparesis: a review of new developments
- The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia
- Southern Regional Meeting Abstracts
- A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members
- Spastin gene mutation in Japanese with hereditary spastic paraplegia
- Cardiomyopathy in motor neuron diseases
- Important points in the clinical evaluation of patients with syncope
- Measuring the quality of referral letters about patients with upper gastrointestinal symptoms
- Autopsy confirmed multiple system atrophy cases: Mayo experience and role of autonomic function tests
- Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia