Results 11 to 20 of about 7,103 (220)

Herbal medicine and acupuncture relieved progressive bulbar palsy for more than 3 years: A case report. [PDF]

Medicine (Baltimore), 2022
Rationale: Progressive bulbar palsy (PBP) is a type of motor neuron disease (MND). The main symptoms include dysarthria, dysphagia, tongue muscle atrophy and fasciculations. This disease is generally severe and develops rapidly.
Peng S, Chang W, Tian Y, Yang Y, Li S, Ni J, Zhu W.   +6 more
europepmc   +4 more sources

Infantile progressive bulbar palsy with deafness

Brain and Development, 2002
A 12-month-old boy with progressive cranial nerve palsies followed by ventilatory failure demanding artificial ventilation, generalized muscle weakness, and rapid progression to death at the age of 21 months is described. The patient had normal early development and also apparently normal hearing at presentation of illness but, after 6 months of the ...
Voudris, K.A., Skardoutsou, A., Vagiakou, E.A.   +2 more
openaire   +5 more sources

Acoustic Vowel Metrics as Correlates of Dysphagia and Dysarthria in Brainstem Neurodegenerative Diseases [PDF]

Audiology Research
Background/Objectives: Swallowing and speech rely on shared brainstem circuits coordinating oropharyngeal motor functions. In neurodegenerative diseases affecting the brainstem—such as progressive supranuclear palsy (PSP), amyotrophic lateral sclerosis ...
Silvia Capobianco, Luca Bastiani, Francesca Forli, Bruno Fattori, Francesco Stomeo, Maria Russo, Maria Rosaria Barillari, Andrea Nacci   +7 more
doaj   +2 more sources

Traditional Chinese Medicine-based Acupuncture and Its Solitary Role in Replenishing Spleen Yin in Facilitating Yoga Rehabilitation in Progressive Bulbar Palsy: A Case Report

Journal of Acupuncture Research
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., Monicaasun M.R., Anbudasan J.   +2 more
doaj   +3 more sources

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

Frontiers 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, Philippe Rochigneux, Alexandre Bertucci, Elika Loir, Alexia Mattei, Danielle Robert, Michael Dassa, Brice Chanez, Mikael Ebbo, Lea Gaigne, Anne Sophie Chretien, Giovanni Corazza, Giovanni Corazza, Nicolas Schleinitz   +13 more
doaj   +3 more sources

Progressive Bulbar Palsy [PDF]

, 2020
National Cancer Institute
openalex   +2 more sources

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

Arquivos 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, Andrea Garcia de Almeida, Magda Lahorgue Nunes, Paulo Márcio Condessa Pitrez, João Arthur Ehlers   +4 more
doaj   +2 more sources

Progressive respiratory depression and bulbar palsy: Question [PDF]

Journal of Clinical Neuroscience, 2016
Caitriona Logan, Hamed Asadi, Hong Kuan Kok, Frances Alexandria Kavanagh, John Thornton, Seamus Looby, Paul Brennan, Alan O’Hare   +7 more
openalex   +2 more sources

“Non-Progressive” Bulbar Palsy [PDF]

Proceedings of the Royal Society of Medicine, 1927
C. Worster‐Drought
openalex   +2 more sources

A Korean family with AGel amyloidosis presenting with progressive facial and bulbar palsies [PDF]

Annals of Clinical Neurophysiology, 2022
AGel amyloidosis is an autosomal dominantly inherited disease caused by a GSN mutation, and affected patients typically present with the clinical triad of corneal lattice dystrophy, progressive cranial neuropathy, and cutis laxa. We report a Korean family with AGel amyloidosis with predominant manifestations of facial and bulbar muscle weakness.
Minsung Kang, Jin‐Hong Shin, Dae‐Seong Kim   +2 more
openalex   +2 more sources