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Abnormal pyramidal signs
Known as:
Pyramidal tracts signs
, Pyramidal signs
, Pyramidal tract signs
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Functional neurological abnormalities related to dysfunction of the pyramidal tract. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
50 relations
3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
Basal ganglia disease, biotin-responsive
Behr syndrome
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Adult Cases of Leukoencephalopathy, Cerebral Calcifications, and Cysts: Expanding the Spectrum of the Disorder
B. Kleinschmidt-DeMasters
,
T. Cummings
,
C. Hulette
,
J. Morgenlander
,
J. Corboy
Journal of Neuropathology and Experimental…
2009
Corpus ID: 13470415
Leukoencephalopathy with cerebral calcifications and cysts (LCC) was first reported in children who developed cognitive decline…
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Highly Cited
1998
Highly Cited
1998
Parietal motor syndrome: A clinical description in 32 patients in the acute phase of pure parietal strokes studied prospectively
J. Ghika
,
F. Ghika-Schmid
,
J. Bogousslasvky
Clinical neurology and neurosurgery (Dutch…
1998
Corpus ID: 25276165
1996
1996
Machado-Joseph disease and SCA3
L. Junck
,
J. Fink
Neurology
1996
Corpus ID: 28677487
Neurology 1996;46:4-8 Based on initial descriptions, Machado-Joseph disease (MJD) was thought to be a distinct clinicopathologic…
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1995
1995
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family
A. Filla
,
G. Michele
,
+8 authors
S. Cocozza
Neurology
1995
Corpus ID: 28076555
Article abstract-The gene for spinocerebellar ataxia type 2 (SCA2) is mapped to chromosome 12q23-24.1. Using D12S79 and D12S105…
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Highly Cited
1994
Highly Cited
1994
Lessons from a remarkable family with dopa-responsive dystonia.
G. Harwood
,
R. Hierons
,
N. Fletcher
,
C. Marsden
Journal of Neurology Neurosurgery & Psychiatry
1994
Corpus ID: 138411
A family is described in which dopa-responsive dystonia affected six members and segregated in an autosomal dominant fashion…
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1991
1991
Motor evoked potentials (MEPs) in lacunar syndromes.
G. Abbruzzese
,
M. Morena
,
D. Dall’agata
,
M. Abbruzzese
,
E. Favale
Electroencephalography and Clinical…
1991
Corpus ID: 45022349
1982
1982
Carbon disulfide-induced neuropsychiatric changes in grain storage workers.
Henry A. Peters
,
Ross L. Levine
,
Charles G. Matthews
,
Steven L. Sauter
,
John H.G. Rankin
American Journal of Industrial Medicine
1982
Corpus ID: 27397007
The clinical and neuropsychiatric features of seven workers from the grain storage industry are described. All were exposed to…
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1977
1977
Macular cherry-red spots and beta-galactosidase deficiency in an adult. An autopsy case with progressive cerebellar ataxia, myoclonus, thrombocytopathy, and accumulation of polysaccharide in liver.
Y. Suzuki
,
N. Nakamura
,
Y. Shimada
,
H. Yotsumoto
,
H. Endo
,
K. Nagashima
Archives of Neurology
1977
Corpus ID: 23395852
An adult patient with macular cherry-red spots, a gargoyle-like physical appearance, cerebellar ataxia, myoclonus, convulsive…
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Highly Cited
1970
Highly Cited
1970
Brain stem tumors of childhood and adolescence.
H. Panitch
,
B. Berg
A M A Journal of Diseases of Children
1970
Corpus ID: 33636484
Forty children and adolescents showed clinical and radiographic evidence of brain stem tumors. The typical case is characterized…
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Review
1962
Review
1962
Seizure disorders in a Guamanian village.
S. Lessell
,
J. Torres
,
L. Kurland
Archives of Neurology
1962
Corpus ID: 2308034
Introduction For the past 10 years the National Institute of Neurological Diseases and Blindness, through its Epidemiology Branch…
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