Results 91 to 100 of about 4,302 (188)
A 52-year old woman first noted dysphagia four months before admission followed by dysarthria two months later. She then developed weakness of all limbs and became unable to walk. All these symptoms, associated with tongue atrophy, slowly progressed, leading to the initial clinical impression of a motor neuron disease, although her nerve conduction ...
Kiyoaki, Takeda +4 more
openaire +3 more sources
Gelsolin variant amyloidosis mimicking progressive bulbar palsy
Jinseok Park +6 more
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Progressive bulbar palsy is a motor neuron disorder characterized by the premature degeneration of motor neurons leading to muscular weakness. A 60-year-old female with complaints of difficulty swallowing even liquids, breathlessness, slurred speech ...
Kavitha Venkatachalam V. +2 more
doaj +1 more source
Aberrant dynamic functional network connectivity in progressive supranuclear palsy
Background: The clinical symptoms of progressive supranuclear palsy (PSP) may be mediated by aberrant dynamic functional network connectivity (dFNC). While earlier research has found altered functional network connections in PSP patients, the majority of
Junyu Qu +7 more
doaj +1 more source
Effects of anodal transcranial direct current stimulation on cognitive dysfunction in patients with progressive supranuclear palsy [PDF]
Progressive supranuclear palsy (PSP) is a tauopathy characterized by motor, neurobehavioral and disabling brainstem deficits. No disease-modifying therapeutic options exist.
Deftereos, S. +8 more
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A case report of dysphagia and cervical muscle weakness along with predominant bulbar palsy as the initial presentation of systemic lupus erythematosus [PDF]
Background: Neuropsychiatric disorders are among the known complications of systemic lupus erythematosus (SLE). The involvement of both peripheral and central nervous systems has also been reported in SLE.Case Report: A 32 year-old woman presented with ...
Khazaei, M., Mazdeh, M.
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[Progressive bulbar palsy (Fazio-Londe disease): case report].
Progressive bulbar palsy, also called Fazio -Londe disease, is characterized by progressive impairment of cranial nerves in children. It was first reported by Fazio in 1892 and until now only 30 cases have been published in the literature. Both sexes can be affected and clinical course can be divided on early (< 6 years age, predominance of respiratory
Bianca Helena Brum, Batista +4 more
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Latest progress and challenges in drug development for degenerative motor neuron diseases
Motor neuron diseases are sporadic or inherited fatal neurodegenerative conditions. They selectively affect the upper and/or lower motor neurons in the brain and spinal cord and feature a slow onset and a subacute course contingent upon the site of ...
Xiangjin Wen +5 more
doaj +1 more source
The researchersWe report on a patient with progressive bulbar palsy (PBP) who presented with Broca’s aphasia due to injury of the left arcuate fasciculus (AF), as demonstrated on diffusion tensor tractography (DTT). A 74-yearold right handed patient with PBP and six age-matched normal subjects were recruited for this study.
openaire +1 more source
Unsupervised Machine Learning Approach to Discover Subtypes of Progressive Supranuclear Palsy [PDF]
Progressive supranuclear palsy (PSP) is a rare, rapidly progressive, neurodegenerative disease characterised by ocular motor abnormalities, postural instability, parkinsonism and cognitive dysfunctions.
M. Russo +8 more
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