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Neurology
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Spastic paraplegia

Citations 51-60 of 62 total displayed.

Past content (since Jan 2001):

ARTICLES
IgG in brain correlates with clinicopathological damage in HTLV-1 associated neurologic disease
M. Jernigan, Y. Morcos, S.M. Lee, F.C. Dohan, Jr., C. Raine, and M.C. Levin
Neurology 2003; 60: 1320-1327. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Pure spastic paraparesis associated with a novel presenilin 1 R278K mutation
A. Assini, L. Terreni, R. Borghi, L. Giliberto, A. Piccini, D. Loqui, S. Fogliarino, G. Forloni, and M. Tabaton
Neurology 2003; 60: 150. [Full text] [PDF]  

ARTICLES
A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14
C. A. Hodgkinson, S. Bohlega, S. N. Abu–Amero, E. Cupler, M. Kambouris, B. F. Meyer, and V. A. Bharucha
Neurology 2002; 59: 1905-1909. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
SPG3A: An additional family carrying a new atlastin mutation
A. Tessa, C. Casali, M. Damiano, C. Bruno, D. Fortini, C. Patrono, F. Cricchi, M. Valoppi, G. Nappi, G.A. Amabile, E. Bertini, and F.M. Santorelli
Neurology 2002; 59: 2002-2005. [Abstract] [Full text] [PDF]  

ARTICLES
Clinical and genetic study of a large Italian family linked to SPG12 locus
A. Orlacchio, T. Kawarai, E. Rogaeva, Y.Q. Song, A.D. Paterson, G. Bernardi, and P.H. St. George-Hyslop
Neurology 2002; 59: 1395-1401. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities
S. O’Riordan, P. McMonagle, J. C. Janssen, N. C. Fox, M. Farrell, J. Collinge, M. N. Rossor, and M. Hutchinson
Neurology 2002; 59: 1108-1110. [Abstract] [Full text] [PDF]  

ARTICLES
X-linked myoclonic epilepsy with spasticity and intellectual disability: Mutation in the homeobox gene ARX
I. E. Scheffer, R. H. Wallace, F. L. Phillips, P. Hewson, K. Reardon, G. Parasivam, P. Stromme, S. F. Berkovic, J. Gecz, and J. C. Mulley
Neurology 2002; 59: 348-356. [Abstract] [Full text] [PDF]  

ARTICLES
Spastic paraplegia, ataxia, mental retardation (SPAR): A novel genetic disorder
P. Hedera, S. Rainier, X. P. Zhao, M. Schalling, K. Lindblad, Q-P. Yuan, T. Ikeuchi, J. Trobe, J. J. Wald, O. P. Eldevik, K. Kluin, and J. K. Fink
Neurology 2002; 58: 411-416. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Diagnosis of HAM/TSP based on CSF proviral HTLV-I DNA and HTLV-I antibody index
M. Puccioni–Sohler, M. Rios, S. M. F. Carvalho, R. R. Gonçalves, C. Oliveira, R. B. Correa, S. Novis, M. S. Pombo de Oliveira, and C. Bianco
Neurology 2001; 57: 725-727. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Natural history of an incidentally discovered spinal dural arteriovenous fistula
Emmanuel Houdart, Aimée Redondo, Jean-Pierre Saint-Maurice, and Jean-Jacques Merland
Neurology 2001; 57: 742-743. [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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