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Neurology
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Spastic paraplegia

Citations 1-10 of 62 total displayed.

Most recent content (6 Oct 2009):

ARTICLES
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
C. Goizet, A. Boukhris, D. Maltete, L. Guyant-Maréchal, J. Truchetto, E. Mundwiller, S. Hanein, P. Jonveaux, F. Roelens, J. Loureiro, E. Godet, S. Forlani, J. Melki, M. Auer-Grumbach, J. C. Fernandez, P. Martin-Hardy, I. Sibon, G. Sole, I. Orignac, C. Mhiri, P. Coutinho, A. Durr, A. Brice, and G. Stevanin
Neurology 2009; 73: 1111-1119. [Abstract] [Full text] [PDF]  

Past content (since Jan 2001):

CLINICAL/SCIENTIFIC NOTES
16p11.2-RELATED PAROXYSMAL KINESIGENIC DYSKINESIA AND DOPA-RESPONSIVE PARKINSONISM IN A CHILD
Jonathan Lipton and Michael J. Rivkin
Neurology 2009; 73: 479-480. [Full text] [PDF]  

ARTICLES
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24
R. Schüle, M. Bonin, A. Dürr, S. Forlani, A. D. Sperfeld, S. Klimpe, J. C. Mueller, A. Seibel, B. P. van de Warrenburg, P. Bauer, and L. Schöls
Neurology 2009; 72: 1893-1898. [Abstract] [Full text] [PDF]  

EDITORIALS
Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia
John K. Fink
Neurology 2008; 71: 1468-1469. [Full text] [PDF]  

ARTICLES
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
F. Brugman, H. Scheffer, J.H.J. Wokke, W. M. Nillesen, M. de Visser, E. Aronica, J. H. Veldink, and L. H. van den Berg
Neurology 2008; 71: 1500-1505. [Abstract] [Full text] [PDF]  

ARTICLES
SPG11 compound mutations in spastic paraparesis with thin corpus callosum
L. Samaranch, M. Riverol, J. C. Masdeu, E. Lorenzo, J. M. Vidal-Taboada, J. Irigoyen, M. A. Pastor, P. de Castro, and P. Pastor
Neurology 2008; 71: 332-336. [Abstract] [Full text] [PDF]  

EDITORIALS
Genetic testing for the spastic paraplegias: Drowning by numbers
Alexandra Dürr
Neurology 2008; 71: 236-238. [Full text] [PDF]  

ARTICLES
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23
K. J. Dick, R. Al-Mjeni, W. Baskir, R. Koul, M. A. Simpson, M. A. Patton, S. Raeburn, and A. H. Crosby
Neurology 2008; 71: 248-252. [Abstract] [Full text] [PDF]  

ARTICLES
Two-year placebo-controlled trial of botulinum toxin A for leg spasticity in cerebral palsy
A. P. Moore, R. A. Ade-Hall, C. Tudu Smith, L. Rosenbloom, H.P.J. Walsh, K. Mohamed, and P. R. Williamson
Neurology 2008; 71: 122-128. [Abstract] [Full text] [PDF]  

ARTICLES
Silver syndrome variant of hereditary spastic paraplegia: A locus to 4p and allelism with SPG4
A. Orlacchio, C. Patrono, F. Gaudiello, C. Rocchi, V. Moschella, R. Floris, G. Bernardi, and T. Kawarai
Neurology 2008; 70: 1959-1966. [Abstract] [Full text] [PDF]  

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 Movement Disorders
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 Motor cortex
 Stiff person syndrome
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 Spastic paraplegia


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