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Neurology
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Spastic paraplegia

Citations 31-40 of 62 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology
S. Papapetropoulos, T. Scaravilli, H. Morris, S. F. An, D. C. Henderson, N. P. Quinn, F. Scaravilli, and K. P. Bhatia
Neurology 2005; 64: 731-733. [Abstract] [Full text] [PDF]  

ARTICLES
Diffusion tensor imaging for the assessment of upper motor neuron integrity in ALS
J. M. Graham, N. Papadakis, J. Evans, E. Widjaja, C. A.J. Romanowski, M. N.J. Paley, L. I. Wallis, I. D. Wilkinson, P. J. Shaw, and P. D. Griffiths
Neurology 2004; 63: 2111-2119. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Hereditary spastic paraplegia with frontal lobe dysfunction: A clinicopathologic study
D. Yanase, K. Komai, T. Hamaguchi, S. Okino, H. Yokoji, T. Makifuchi, H. Takano, and M. Yamada
Neurology 2004; 63: 2149-2152. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Acquired hepatocerebral degeneration without overt liver disease
M. A.C. Saporta, C. André, P. R.V. Bahia, L. Chimelli, P. H.N. Pais, T. S. Silva, A. H.P. Correia, and A. B. Nobre
Neurology 2004; 63: 1981-1982. [Full text] [PDF]  

VIEWS & REVIEWS
Oral antispastic drugs in nonprogressive neurologic diseases: A systematic review
E. Montané, A. Vallano, and J. R. Laporte
Neurology 2004; 63: 1357-1363. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia
M. Fichera, M. Lo Giudice, M. Falco, M. Sturnio, S. Amata, O. Calabrese, S. Bigoni, E. Calzolari, and M. Neri
Neurology 2004; 63: 1108-1110. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene
P. F. Chinnery, S. M. Keers, M. J. Holden, V. Ramesh, and A. Dalton
Neurology 2004; 63: 710-712. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene
A. D’Amico, A. Tessa, A. Sabino, E. Bertini, F. M. Santorelli, and S. Servidei
Neurology 2004; 62: 2138-2139. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis
P. Moretti, A. P. Lieberman, E. A. Wilde, B. I. Giordani, K. J. Kluin, R. A. Koeppe, S. Minoshima, D. E. Kuhl, W. K. Seltzer, and N. L. Foster
Neurology 2004; 62: 1865-1868. [Abstract] [Full text] [PDF]  

ARTICLES
Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia
Paul McMonagle, Paula Byrne, and Michael Hutchinson
Neurology 2004; 62: 407-410. [Abstract] [Full text] [PDF]  

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* Related collections:
 Movement Disorders
 All Movement Disorders
 Dystonia
 Blepharospasm
 Gait disorders/ataxia
 Cerebellum
 Huntington's disease
 Basal ganglia
 Parkinson's disease/Parkinsonism
 Motor Control
 Progressive supranuclear palsy
 Motor cortex
 Stiff person syndrome
 Surgery/Stimulation
 Tourette syndrome
 Tremor
 Tics
 Chorea
 Botulinum toxin
 Multiple system atrophy
 Rett Syndrome
 Myoclonus
 Spastic paraplegia


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