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Spastic paraplegia
Citations 21-30 of 62 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
The Spastic Paraplegia Rating Scale (SPRS): A reliable and valid measure of disease severity
- R. Schüle, T. Holland-Letz, S. Klimpe, J. Kassubek, T. Klopstock, V. Mall, S. Otto, B. Winner, and L. Schöls
Neurology 2006; 67: 430-434.
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- ARTICLES
The natural history of primary lateral sclerosis
- P. H. Gordon, B. Cheng, I. B. Katz, M. Pinto, A. P. Hays, H. Mitsumoto, and L. P. Rowland
Neurology 2006; 66: 647-653.
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- ARTICLES
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia
- N. Elleuch, C. Depienne, A. Benomar, A. M. Ouvrard Hernandez, X. Ferrer, B. Fontaine, D. Grid, C.M.E. Tallaksen, R. Zemmouri, G. Stevanin, A. Durr, and A. Brice
Neurology 2006; 66: 654-659.
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- BRIEF COMMUNICATIONS
Unexpected pathogenic mechanism of a novel mutation in the coding sequence of SPG4 (spastin)
- J. Schickel, C. Beetz, C. Frömmel, G. Heide, A. Sasse, P. Hemmerich, and T. Deufel
Neurology 2006; 66: 421-423.
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- BRIEF COMMUNICATIONS
Dementia, pyramidal system involvement, and leukoencephalopathy with a presenilin 1 mutation
- M. G. Marrosu, G. Floris, G. Costa, L. Schirru, G. Spinicci, M. V. Cherchi, M. Mura, M. G. Mascia, and E. Cocco
Neurology 2006; 66: 108-111.
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- BRIEF COMMUNICATIONS
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
- M. Namekawa, P. Ribai, I. Nelson, S. Forlani, F. Fellmann, C. Goizet, C. Depienne, G. Stevanin, M. Ruberg, A. Dürr, and A. Brice
Neurology 2006; 66: 112-114.
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- NEUROIMAGES
Kjellin syndrome: First case with retinal changes in carriers
- Arun Sachdev, Frank A. Proudlock, Richard Abbott, and Irene Gottlob
Neurology 2005; 65: 1110.
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- BRIEF COMMUNICATIONS
Early-onset ALS with long-term survival associated with spastin gene mutation
- T. Meyer, A. Schwan, J. S. Dullinger, J. Brocke, K. -T. Hoffmann, C. H. Nolte, A. Hopt, U. Kopp, P. Andersen, J. T. Epplen, and P. Linke
Neurology 2005; 65: 141-143.
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- BRIEF COMMUNICATIONS
A phenotype without spasticity in sacsin-related ataxia
- H. Shimazaki, Y. Takiyama, K. Sakoe, Y. Ando, and I. Nakano
Neurology 2005; 64: 2129-2131.
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- ARTICLES
Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy
- A. Fatemi, S. A. Smith, P. Dubey, K. M. Zackowski, A. J. Bastian, P. C. van Zijl, H. W. Moser, G. V. Raymond, and X. Golay
Neurology 2005; 64: 1739-1745.
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