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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

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Related topics

1 relation
CNS disorder

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.
BACKGROUND Hereditary spastic paraparesis (HSP) (syn. Hereditary spastic paraplegia, SPG) are a group of genetic disorders… Expand
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2010
2010
Two Australian families with inclusion-body myopathy, Paget’s disease of bone and frontotemporal dementia: Novel clinical and genetic findings
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
Pyramidal tract degeneration in multiple system atrophy: the relevance of magnetization transfer imaging.
The clinical features of multiple system atrophy (MSA) include four domains: autonomic failure/urinary dysfunction, Parkinsonism… Expand
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2004
2004
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
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
Disease modifying therapies in multiple sclerosis: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology and the MS Council for Clinical Practice…
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
The Stiff-Person Syndrome: An Autoimmune Disorder Affecting Neurotransmission of -Aminobutyric Acid
Dr. Dalakas (Neuromuscular Diseases Section, National Institutes of Neurological Diseases and Stroke [NINDS], National Institutes… Expand
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1996
1996
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration (PPND) is a… Expand
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1996
1996
Motor neuron disease with pyramidal tract dysfunction involves the cortical generators of the early somatosensory evoked potential to tibial nerve stimulation.
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
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
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
Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features.
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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