Results 181 to 190 of about 7,103 (220)

The clinical course of progressive bulbar palsy

open access: closedAmyotrophic Lateral Sclerosis, 2010
Our objective was to study the clinical course of patients diagnosed with progressive bulbar palsy (PBP). We reviewed all 392 medical records of ALS patients seen between 1 January 2000 and 31 July 2007. Patients with isolated PBP at presentation were selected and classified into those with normal EMG of the limbs (PBP-N) and those with active ...
Chafic Karam   +2 more
exaly   +5 more sources

Juvenile Progressive Bulbar Palsy

open access: closedArchives of Neurology, 1983
Differentiation of juvenile progressive bulbar palsy from bulbar myasthenia gravis is difficult. Characteristics of both may include ocular involvement, fluctuant course, abnormal fatigability, and normal acetylcholine receptor (AChR) antibody titers.
James W. Albers
exaly   +5 more sources

Progressive bulbar palsy: a case report diagnosed by lingual symptoms

open access: closedJournal of Oral Pathology & Medicine, 2002
AbstractThe aim of this report is to show a case of Progressive Bulbar Palsy (PBP), diagnosed by oral medicine specialists, from oral symptoms of the disease. We have found no more than two published cases of PBP diagnosed by lingual alterations.
Rocío Cerero Lapiedra   +2 more
exaly   +5 more sources

A - 101 A Neuropsychological Case Study of Progressive Bulbar Palsy

open access: closedArchives of Clinical Neuropsychology, 2023
Abstract Objective There has been limited literature regarding cognitive dysfunction associated with progressive bulbar palsy. This case study presents the neuropsychological profile of a 66-year-old White male diagnosed with progressive bulbar palsy (evolving primary lateral sclerosis) with speech ...
Sarah E Kysor-Itri, V Sekunda
openalex   +2 more sources

Progressive Bulbar Palsy

open access: closed, 2008
Marc D. Binder   +2 more
openalex   +2 more sources

Progressive ponto-bulbar palsy with deafness. A clinico-pathological study.

Acta neurologica Belgica, 1977
Progressive ponto-bulbar palsy with deafness is a rare disease. It seems to be an abiotrophic process with autosomal recessive inheritance in most instances. Only one autopsy case had been briefly described (Lelong et al., 1941). The clinical features and the pathological findings of a new case are reported.
A, Lombaert   +3 more
openaire   +2 more sources

Progressive bulbar palsy: A case report of a type of motor neuron disease presenting with oral symptoms

open access: closedOral Surgery, Oral Medicine, Oral Pathology, 1990
A case is presented of a patient with progressive bulbar palsy, a form of motor neuron disease, which is a progressive degenerative disorder of the motor nuclei in the medulla producing atrophy and fasciculations of the musculature of the tongue, dysarthria, dysphagia, and excessive accumulation of secretions.
Anna Talacko, Peter C. Reade
openalex   +3 more sources

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