Amyotrophic lateral sclerosis -plus patient with an intermediate-length CACNA1A allele: a Case Report [PDF]
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
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]
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]
Progressive respiratory depression and bulbar palsy ...
C. Logan +7 more
openaire +2 more sources
Progressive respiratory depression and bulbar palsy: Answer [PDF]
Progressive respiratory depression and bulbar palsy ...
C. Logan +7 more
openaire +2 more sources
The first description of idiopathic progressive bulbar palsy. [PDF]
A M Chancellor +2 more
exaly +3 more sources
Basilar invagination: A mimicker of bulbar-onset amyotrophic lateral sclerosis
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]
[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]
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]
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

