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Pseudobulbar signs
Known as:
Pseudobulbar symptoms
Pseudobulbar signs result from injury to an upper motor neuron lesion to the corticobulbar pathways in the pyramidal tract. Patients have difficulty…
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National Institutes of Health
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Related topics
Related topics
3 relations
Angiomatosis, diffuse corticomeningeal, of Divry and Van Bogaert
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Spastic Paraplegia-50, Autosomal Recessive
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
Clinical aspects and pathology of Alexander disease, and morphological and functional alteration of astrocytes induced by GFAP mutation
Tomokatsu Yoshida
,
M. Nakagawa
Neuropathology (Kyoto. )
2012
Corpus ID: 7714145
Alexander disease (AxD) is pathologically characterized by the presence of Rosenthal fibers (RF), which are made up of GFAP, αB…
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2010
2010
The use of zolpidem in the treatment of progressive supranuclear palsy
C. Cotter
,
T. Armytage
,
D. Crimmins
Journal of clinical neuroscience
2010
Corpus ID: 404215
Highly Cited
1999
Highly Cited
1999
The emotional lability questionnaire: a new measure of emotional lability in amyotrophic lateral sclerosis
I. Newsom-Davis
,
S. Abrahams
,
L. Goldstein
,
P. Leigh
Journal of Neurological Sciences
1999
Corpus ID: 38288918
1999
1999
Quantitative voice analysis in the assessment of bulbar involvement in amyotrophic lateral sclerosis.
Danièle Robert
,
Jean Pouget
,
Antoine Giovanni
,
J. Azulay
,
J. Triglia
Acta Oto-Laryngologica
1999
Corpus ID: 44953107
Bulbar and pseudobulbar symptoms are diagnostic criteria of amyotrophic lateral sclerosis (ALS). One of the earliest symptoms of…
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Highly Cited
1999
Highly Cited
1999
Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.
P. Coutinho
,
J. Barros
,
+13 authors
D. Grid
Archives of Neurology
1999
Corpus ID: 11496015
BACKGROUND Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders characterized by…
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1997
1997
Early infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies
D. Zafeiriou
,
A. Anastasiou
,
E. Michelakaki
,
P. Augoustidou-Savvopoulou
,
G. Katzos
,
E. Kontopoulos
Brain & development (Tokyo. )
1997
Corpus ID: 21467616
Highly Cited
1997
Highly Cited
1997
Cystic leukoencephalopathy in a megalencephalic child: clinical and magnetic resonance imaging/magnetic resonance spectroscopy findings.
V. Mejaški‐Bošnjak
,
N. Bešenski
,
K. Brockmann
,
P. Pouwels
,
J. Frahm
,
F. Hanefeld
Pediatric Neurology
1997
Corpus ID: 11031755
Highly Cited
1997
Highly Cited
1997
Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients.
A. Gropman
,
A. Barkovich
,
L. Vezina
,
J. Conry
,
E. Dubovsky
,
R. Packer
Neuropediatrics
1997
Corpus ID: 34479088
In 1926, Foix, Chavany and Marie described an acquired syndrome of fasciopharyngoglossomasticatory diplegia resulting from…
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1996
1996
Mutism and pseudobulbar symptoms after resection of posterior fossa tumors in children: incidence and pathophysiology and transient cerebellar mutism after posterior fossa surgery in children.
L. Mastronardi
Neurosurgery
1996
Corpus ID: 37176689
1984
1984
Evolution of central pontine myelinolysis on CT.
Shelley Rosenbloom
,
D. Buchholz
,
Ashok J. Kumar
,
Richard A. Kaplan
,
Hamilton Moses
,
ArthurE. Rosenbaum
AJNR. American journal of neuroradiology
1984
Corpus ID: 9981970
Central pontine myelinolysis (CPM) was first described by Adams et al. [1] in 1959; since then , well over 100 cases have been…
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