Results 41 to 50 of about 25,100 (235)

Disease duration of progression is helpful in identifying isolated bulbar palsy of amyotrophic lateral sclerosis [PDF]

open access: yesBMC Neurology, 2021
Abstract Background Compared with typical bulbar onset amyotrophic lateral sclerosis (ALS), isolated bulbar palsy (IBP), an often under-understood variant of ALS, is characterized by symptoms confined to bulbar region for extended periods and relative preservation of limb and ventilation function.
Huagang Zhang   +3 more
openaire   +3 more sources

Fazio Londe syndrome: A treatable disorder

open access: yesAnnals of Indian Academy of Neurology, 2015
Fazio Londe Syndrome is a rare neurological disorder presenting with progressive bulbar palsy with respiratory failure. Initially considered to have an unrelenting course, is now found to be due to mutations in the SLC52A3 gene which encodes the ...
Poovazhagi Varadarajan   +2 more
doaj   +1 more source

Correlation Between Maximal Tongue Pressure and Swallowing Function in Spinal and Bulbar Muscular Atrophy

open access: yesFrontiers in Neurology, 2021
Background: Spinal and bulbar muscular atrophy (SBMA) is an X-lined motor neuron disease characterized by progressive muscle weakness, bulbar palsy, and dysphagia.
Dae-Won Gwak   +7 more
doaj   +1 more source

Accuracy of routinely-collected healthcare data for identifying motor neurone disease cases: a systematic review [PDF]

open access: yes, 2017
Background Motor neurone disease (MND) is a rare neurodegenerative condition, with poorly understood aetiology. Large, population-based, prospective cohorts will enable powerful studies of the determinants of MND, provided identification of disease cases
Horrocks, Sophie   +5 more
core   +1 more source

IgLON5-Associated Encephalitis With Atypical Brain Magnetic Resonance Imaging and Cerebrospinal Fluid Changes

open access: yesFrontiers in Neurology, 2018
IgLON5-associated encephalitis is a syndrome with different clinical presentations consisting of sleep dysfunction, bulbar dysfunction, chorea, and progressive supranuclear palsy-like symptoms whereas dysautonomy and cognitive decline usually appear in ...
Massimiliano Montagna   +8 more
doaj   +1 more source

Clinical and imaging features of "heart appearance" isolated cerebral infarction in bilateral medial pons-medulla oblongata

open access: yes陆军军医大学学报, 2023
Objective To investigate the clinical and imaging features of the characteristic "heart appearance" isolated cerebral infarction involving bilateral pons-medulla oblongata.
DIAO Shengpeng   +4 more
doaj   +1 more source

Tremor in motor neuron disease may be central rather than peripheral in origin [PDF]

open access: yes, 2018
BACKGROUND AND PURPOSE: Motor neuron disease (MND) refers to a spectrum of degenerative diseases affecting motor neurons. Recent clinical and post-mortem observations have revealed considerable variability in the phenotype.
Balint, B   +9 more
core   +2 more sources

Apraxia and motor dysfunction in corticobasal syndrome [PDF]

open access: yes, 2014
Background: Corticobasal syndrome (CBS) is characterized by multifaceted motor system dysfunction and cognitive disturbance; distinctive clinical features include limb apraxia and visuospatial dysfunction. Transcranial magnetic stimulation (TMS) has been
A Alberici   +79 more
core   +3 more sources

Fatal subarachnoid hemorrhage following ischemia in vertebrobasilar dolichoectasia. [PDF]

open access: yes, 2016
Vertebrobasilar dolichoectasia (VBD) is a chronic disorder with various cerebrovascular and compressive manifestations, involving subarachnoid hemorrhage (SAH).
Caso, V.   +10 more
core   +7 more sources

Progress and challenges in directing the differentiation of human iPSCs into spinal motor neurons

open access: yesFrontiers in Cell and Developmental Biology, 2023
Motor neuron (MN) diseases, including amyotrophic lateral sclerosis, progressive bulbar palsy, primary lateral sclerosis and spinal muscular atrophy, cause progressive paralysis and, in many cases, death.
Cristina Marisol Castillo Bautista   +2 more
doaj   +1 more source

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