Results 21 to 30 of about 9,800 (213)
Journal of International Medical Research, 2023 Guillain–Barré syndrome (GBS) and Miller Fisher syndrome (MFS) are acute immune-mediated peripheral neuropathies. In addition to their classic presentations, a variety of other signs and symptoms have been reported; however, headache appears to be ...
Ming Chi, Lu Han, Zilong Zhu
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Basilar invagination: A mimicker of bulbar-onset amyotrophic lateral sclerosis
eNeurologicalSci, 2021 Amyotrophic lateral sclerosis (ALS) is characterized by progressive onset motor deficits with heterogenous presentations ranging from dysarthria to foot drop.
Jason Seng Hong Tan +2 more
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Congenital oculo-bulbar palsy. [PDF]
Journal of Neurology, Neurosurgery & Psychiatry, 1992 A girl developed progressive weakness of bulbar and ocular muscles starting before the age of two years. Electromyography revealed a widespread subclinical myopathy. An intercostal muscle biopsy showed complex abnormalities including occasional neurofilamentous accumulations and honeycomb-like membranous material in terminal axons. Endplates were small
F G, Jennekens +4 more
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Developmental Medicine & Child Neurology, 1969 SUMMARYProgressive bulbar palsy is very rare in childhood. A probable case diagnosed in Greece is presented. After a short review of the literature the clinical and laboratory findings are described. The main clinical features were progressive affection of the bulbar nuclei over one year without involvement of the long tracts.
Gregoriou, M. +2 more
openaire +3 more sources
Isolated Bulbar Palsy: A Rare Presentation of Neurosarcoidosis. [PDF]
Cureus, 2020 Sarcoidosis, which is a non-caseating granulomatous chronic inflammatory disease, can affect virtually any organ system, including the central nervous system (CNS). Very rarely, patients may present solely with neurosarcoidosis. It commonly presents with unilateral or bilateral seventh nerve palsy.
Chaudhry HS +4 more
europepmc +4 more sources
Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases [PDF]
, 2017 Objective: To examine the utility of the new Movement Disorder Society (MDS) diagnostic criteria in a large cohort of Parkinson's disease (PD) patients.
, +13 more
core +5 more sources
Jaw Rotation in Dysarthria Measured With a Single Electromagnetic Articulography Sensor [PDF]
, 2017 Purpose This study evaluated a novel method for characterizing jaw rotation using orientation data from a single electromagnetic articulography sensor.
Berry, Jeffrey +3 more
core +2 more sources
Case 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
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Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis [PDF]
, 2010 The finding of TDP-43 as a major component of ubiquitinated protein inclusions in amyotrophic lateral sclerosis (ALS) has led to the identification of 30 mutations in the transactive response-DNA binding protein (TARDBP) gene, encoding TDP-43.
A Yokoseki +46 more
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Bilateral horizontal gaze palsy due to Anti-IgLON5 disease
American Journal of Ophthalmology Case Reports, 2022 Purpose: To highlight the eye movement disturbances in anti-IgLON5 disease. Methods: Case report. Results: Anti-IgLON5 is a heterogenous neurodegenerative and autoimmune disease manifested by a variety of signs and symptoms including sleep disorder ...
M Tariq Bhatti, MD
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