Palliative Care Challenges of Patients With Progressive Bulbar Palsy: A Retrospective Case Series of 14 Patients [PDF]
Progressive bulbar palsy (PBP) is a form of motoneuron disease and is widely classified as a subtype of amyotrophic lateral sclerosis (ALS) with a shorter time of survival and female predominance. In this retrospective case series of 14 patients with PBP,
Sarah K. Bublitz +8 more
doaj +7 more sources
Creativity and Mental Illness: A Case Study of a Patient with Progressive Bulbar Palsy [PDF]
Creativity and the production of artwork can have an impact on the course and treatment of comorbid severe mental illness and neurodegeneration. We report on a 70-year-old male patient with highly original artistic behavior, who suffered from lifelong ...
Felix Geser +5 more
doaj +6 more sources
A case report on Ayurvedic management of progressive bulbar palsy-A rare amyotrophic lateral sclerosis phenotype [PDF]
This case report is the description of a devastating illness, Progressive Bulbar Palsy (PBP) of a sixty-seven years old male patient. He presented with complaints of slurred speech, hearing impairment, generalised weakness of limbs, weakened grip to hold
Sinimol Thekkekkoottumughath Peethambaran +2 more
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Progressive Bulbar Palsy (PBP) or Bulbar Onset MND: “A Case Report” [PDF]
A patient with enhancing bulbar palsy, a type of efferent neuron disease that causes hypertrophy and twitching of the tongue’s musculature, dysphagia, dysarthria, and an excessive buildup of secretions, is described.
Sagar S. Bhovare, Akhataribano S. Sayyad
doaj +4 more sources
The same cortico-efferent tract involvement in progressive bulbar palsy and in ‘classical’ ALS: A tract of interest-based MRI study [PDF]
Background: There is an ongoing debate about the concept of restricted phenotypes of amyotrophic lateral sclerosis (ALS), including progressive bulbar palsy (PBP).
Hans-Peter Müller +4 more
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Neuro-Behçet’s masquerading as progressive bulbar palsy: a case report and literature review [PDF]
In patients with progressive bulbar palsy without an obvious cause, there should be a high index of suspicion for the potential diagnosis of Neuro-Behçet’s Disease, even in the absence of the acute classical peripheral manifestations of Bechet’s Disease,
Theodoros Paschalis +3 more
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Progressive bulbar palsy with facial diplegia and proximal weakness diagnosed as juvenile-onset myasthenia gravis [PDF]
Rajesh Verma +2 more
doaj +4 more sources
Case report: A severe myositis mimicking bulbar palsy after administration of immune checkpoint inhibitors [PDF]
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 +4 more sources
Case Report: Guillain-Barré syndrome mimicking acute brainstem stroke with severe autonomic dysfunction-complete recovery after early plasma exchange [PDF]
Acute onset of bilateral ptosis, bulbar palsy, and quadriparesis typically raises suspicion for brainstem infarction. However, when neuroimaging is unrevealing, immune-mediated neuropathies such as Guillain-Barré syndrome (GBS) should be considered. This
Jianming Zhu +9 more
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A case report of sporadic Creutzfeldt–Jakob disease presenting with progressive opsoclonus–myoclonus–ataxia-Plus (OMAS-Plus) phenotype [PDF]
Background Sporadic Creutzfeldt–Jakob disease (sCJD) is a rapidly progressive prion disorder whose heterogeneous manifestations may overlap with potentially treatable neurological conditions.
Richard Hulej +5 more
doaj +2 more sources

