FAQ

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… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1962-2018
02419622018

Related topics

Related topics

1 relation
CNS disorder

Related mentions per year

Related mentions per year

1936-2019
19401960198020002020
Pyramidal tract dysfunction
CNS disorder

Papers overview

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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… (More)
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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… (More)
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2009
2009
Tyrosine hydroxylase deficiency with severe clinical course.
Tyrosine hydroxylase (TH) deficiency is a rare autosomal recessive disorder mapped to chromosome 11p15.5. Its clinical expression… (More)
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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… (More)
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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… (More)
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1994
1994
Folate deficiency in cerebrospinal fluid associated with a defect in folate binding protein in the central nervous system.
An adult male patient of Dutch ancestry has a slowly progressive neurological disease characterised by a cerebellar syndrome… (More)
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1992
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… (More)
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1987
1987
Penetration of praziquantel into cerebrospinal fluid and cysticerci in human cysticercosis
Two patients with cysticercosis received praziquantel (PZQ) 75 mg/kg/day orally together with 30 mg prednisone daily for 3 weeks… (More)
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1985
1985
Pyramidal tract deficits and polyneuropathy in hyperthyroidism, Combination clinically mimicking amyotrophic lateral sclerosis.
Generalized weakness, intermittent dysphagia, and a 40-pound weight loss developed in an elderly man over a six-month period… (More)
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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… (More)
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