Results 21 to 30 of about 735,247 (179)

Amyotrophic lateral sclerosis -plus patient with an intermediate-length CACNA1A allele: a Case Report [PDF]

open access: yesFrontiers in Genetics
Amyotrophic lateral sclerosis (ALS), the most common type of motor neuron disease, primarily manifests as progressive weakness, atrophy, fasciculations, bulbar palsy, and pyramidal tract symptoms.
Xinyao Gao   +7 more
doaj   +2 more sources

Colistin induced neurotoxicity with bulbar palsy. A case report and literature review

open access: yesIDCases
Colistin, a polymyxin antibiotic, is increasingly used to manage infections caused by multidrug-resistant gram-negative bacteria. This case report documents the occurrence of colistin-induced neurotoxicity manifesting as bulbar palsy in a 38-year-old ...
Mohamed Kamal Mansour   +2 more
doaj   +2 more sources

Patterns of Laryngeal Changes on Clinical Application of Mechanical Insufflation-Exsufflation Seen with Transnasal Laryngoscopy for Patients with Varied Neurological Conditions and Bulbar Impairment [PDF]

open access: yesEuropean Medical Journal Neurology
Mechanical insufflation-exsufflation (MI-E) is an intervention used for cough augmentation in patients with neurological conditions with bulbar impairment.
Sarah Boggiano   +2 more
doaj   +2 more sources

Progressive respiratory depression and bulbar palsy: Question [PDF]

open access: yesJournal of Clinical Neuroscience, 2016
Progressive respiratory depression and bulbar palsy ...
C. Logan   +7 more
openaire   +2 more sources

Progressive respiratory depression and bulbar palsy: Answer [PDF]

open access: yesJournal of Clinical Neuroscience, 2016
Progressive respiratory depression and bulbar palsy ...
C. Logan   +7 more
openaire   +2 more sources

The first description of idiopathic progressive bulbar palsy. [PDF]

open access: yesJournal of Neurology, Neurosurgery and Psychiatry, 1993
A M Chancellor   +2 more
exaly   +3 more sources

Basilar invagination: A mimicker of bulbar-onset amyotrophic lateral sclerosis

open access: yeseNeurologicalSci, 2021
Amyotrophic lateral sclerosis (ALS) is characterized by progressive onset motor deficits with heterogenous presentations ranging from dysarthria to foot drop.
Jason Seng Hong Tan   +2 more
doaj   +1 more source

Análisis de genes situados en el haplotipo H1 de la región 17q21 y de genes involucrados en la fosforilación de "tau" en la parálisis supranuclear progresiva [PDF]

open access: yes, 2007
[spa] INTRODUCCIÓN: La parálisis supranuclear progresiva (PSP) se caracteriza por el depósito anormal de proteína tau hiperfosforilada en ganglios basales y tronco cerebral.
Campdelacreu i Fumadó, Jaume
core   +6 more sources

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. [PDF]

open access: yes, 2013
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of disorders. A particularly severe subgroup first described in 1894, and subsequently called Brown-Vialetto-Van Laere syndrome, is characterized by progressive ...
Land, John M.   +134 more
core   +2 more sources

A review of the effectiveness of lower limb orthoses used in cerebral palsy [PDF]

open access: yes, 2009
To produce this review, a systematic literature search was conducted for relevant articles published in the period between the date of the previous ISPO consensus conference report on cerebral palsy (1994) and April 2008.
Bowers, R.   +5 more
core   +3 more sources

Home - About - Disclaimer - Privacy