Results 11 to 20 of about 4,302 (188)

Adrenomyeloneuropathy with bulbar palsy: A rare association [PDF]

open access: yesAnnals of Indian Academy of Neurology, 2014
Adrenomyeloneuropathy (AMN) is a variant of adrenoleukodystrophy (ALD), an X-linked recessive peroxisomal disorder associated with accumulation of very long chain fatty acids (VLCFA). Mutations of this gene lead to abnormal peroxisomal β-oxidation, which
Vishal Annaji Chafale   +4 more
doaj   +2 more sources

103 Atypical Progressive Bulbar Palsy presenting with Dropped Head [PDF]

open access: yesCNS Spectrums, 2020
Abstract:Introduction:Typical amyotrophic lateral sclerosis (ALS) presents on neurological examination with specific signs of upper and lower motor neuron degeneration (Brooks et al, 1995), which can account for 85% of patients with ALS (Turner and Talbot, 2013).
Alexander Carvajal-González   +1 more
openaire   +3 more sources

Guillain–Barré syndrome with unilateral peripheral facial and bulbar palsy in a child: A case report [PDF]

open access: yesSAGE Open Medical Case Reports, 2019
Guillain–Barré syndrome is characterized by progressive motor weakness, sensory changes, dysautonomia, and areflexia. Cranial nerve palsies are frequent in Guillain–Barré syndrome.
Kamal Sharma   +4 more
doaj   +2 more sources

Clinical Features of Isolated Bulbar Palsy of Amyotrophic Lateral Sclerosis in Chinese Population [PDF]

open access: yesChinese Medical Journal, 2017
Background: Progressive bulbar palsy (PBP) is a classic phenotype of bulbar onset amyotrophic lateral sclerosis (ALS) with more rapid progression and worse prognosis.
Hua-Gang Zhang   +4 more
doaj   +2 more sources

Acute Thyrotoxic Bulbar Myopathy with Encephalopathic Behaviour: An Uncommon Complication of Hyperthyroidism [PDF]

open access: yesCase Reports in Endocrinology, 2013
Objective. Acute thyrotoxic bulbar palsy is rare, severe, and rapidly progressive. We describe a case of thyrotoxicosis with bulbar palsy, encephalopathy, and pyramidal tract dysfunction. Case Report. 64-year-old white male with toxic multinodular goiter
Neeraja J. Boddu   +4 more
doaj   +2 more sources

Paralisia bulbar progressiva juvenil doença de Fazio-Londe: relato de caso Progressive bulbar palsy (Fazio-Londe disease): case report [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2002
A paralisia bulbar progressiva, também denominada doença de Fazio-Londe, caracteriza-se pelo acometimento degenerativo progressivo de nervos cranianos bulbares em crianças.
Bianca Helena Brum Batista   +4 more
doaj   +2 more sources

Case report: A severe myositis mimicking bulbar palsy after administration of immune checkpoint inhibitors [PDF]

open access: yesFrontiers in Immunology
ObjectivesImmune Checkpoint Inhibitors (ICI) are nowadays a cornerstone of anti-cancer treatments. However, the wide spectrum of immune-related adverse events (irAEs) represents a challenge in the oncological practice.
Philippe Rochigneux   +13 more
doaj   +3 more sources

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

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   +3 more sources

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

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   +4 more sources

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