Results 191 to 200 of about 25,100 (235)

The clinical course of progressive bulbar palsy

Amyotrophic 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 ...
C. Karam, S. Scelsa, D. Macgowan
semanticscholar   +5 more sources

A - 101 A Neuropsychological Case Study of Progressive Bulbar Palsy.

Archives of Clinical Neuropsychology, 2023
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 ...
Sarah E Kysor-Itri, V. Sekunda
semanticscholar   +2 more sources

Juvenile Progressive Bulbar Palsy

Archives 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.
J W, Albers, S, Zimnowodzki, C M, Lowrey, B, Miller   +3 more
openaire   +2 more sources

THE MECHANISMS OF SPEECH AND DEGLUTITION IN PROGRESSIVE BULBAR PALSY

Brain, 1925
M. Critchley, C. Kubik
semanticscholar   +2 more sources

Bulbar Palsy as the Initial Manifestation of Multiple Myeloma: A Case Report.

Journal of the National Medical Association, 2021
Multiple Myeloma (MM) is a neoplastic disorder derived from the malignant proliferation of monoclonal plasma cells. It is characterized by the overproduction of immunoglobulins (Ig).
Shujuan Li, Fang Gao, Weiguo Cheng, S. Wang   +3 more
semanticscholar   +1 more source

Riboflavin responsive progressive bulbar palsy: a Brown-Vialetto-Van Laere Syndrome case report

São Paulo Medical Journal
Introduction: Brown-Vialetto-Van Laere Syndrome (BVVL) is a riboflavin transporter deficiency that usually manifests as neurosensorial deafness followed by progressive bulbar palsy (PBP) in children and young adults.
Luiz Fernando Mohallem Reynaldo, Giovanna Rodrigues dos Santos, Bruno Barros de Pádua Andrade, Rodrigo Ferreira Faria, Gabriel Victor Piai Dall'Oglio, Juliane Patricio Godoy, H. M. T. Andrade   +6 more
semanticscholar   +1 more source

Progressive bulbar palsy: a case report diagnosed by lingual symptoms

Journal 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.
R, Cerero Lapiedra, L A, Moreno López, G C, Esparza Gómez   +2 more
openaire   +2 more sources

The Diagnostic Odyssey: Delayed Identification of Nasopharyngeal Carcinoma Presenting as Bulbar Palsy

Malaysian journal of medicine and health sciences
Nasopharyngeal carcinoma (NPC), predominantly affecting the Chinese population in Malaysia, typically presents with diverse symptoms based on the extent of primary disease and metastasis.
Tze Hui Soo, S. Suppiah, Woon Kian Chai, Wei Sheun Ee   +3 more
semanticscholar   +1 more source

Differences in nerve excitability properties between isolated bulbar palsy and bulbar-dominant amyotrophic lateral sclerosis

Neurological Research, 2020
Objectives: Isolated bulbar palsy (IBP) is a rare variant that can show a benign course, while progressive bulbar palsy (PBP) has been regarded as a bulbar-dominant type of classical amyotrophic lateral sclerosis (cALS).
S. Y. Pyun, Yerim Kim, Seong-il Oh, J. Bae   +3 more
semanticscholar   +1 more source

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, R, Dom, H, Carton, J M, Bruchler   +3 more
openaire   +2 more sources