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Pyramidal tract dysfunction

Known as: Dysfunction of the Pyramidal Tract, Pyramidal tract syndrome 
Dysfunction of the corticospinal (pyramidal) tracts of the spinal cord. Symptoms include increased muscle tone in the lower extremities… Expand
National Institutes of Health

Papers overview

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2014
2014
BACKGROUND Hereditary spastic paraparesis (HSP) (syn. Hereditary spastic paraplegia, SPG) are a group of genetic disorders… Expand
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2010
2010
We report the first Australian families with inclusion-body myopathy, Paget's disease of the bone and frontotemporal dementia… Expand
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2007
2007
The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism… Expand
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2004
2004
Background:Most patients with pure nonprogressive congenital cerebellar ataxia have a sporadic form of unknown heredity and… Expand
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Highly Cited
2002
Highly Cited
2002
MS is a chronic recurrent inflammatory disorder of the CNS. The disease results in injury to the myelin sheaths, the… Expand
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Review
1999
Review
1999
Dr. Dalakas (Neuromuscular Diseases Section, National Institutes of Neurological Diseases and Stroke [NINDS], National Institutes… Expand
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1996
1996
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration (PPND) is a… Expand
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1996
1996
We evaluated somatosensory evoked potentials (SEPs) to tibial nerve stimulation in 39 patients with sporadic motor neuron disease… Expand
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Highly Cited
1992
Highly Cited
1992
We describe a family with nearly 300 members over 8 generations with 32 affected individuals who have an autosomal dominant… Expand
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Highly Cited
1981
Highly Cited
1981
The clinical features of 115 patients from 90 families with Friedreich's ataxia are described. Onset of symptoms was before the… Expand
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