Prediction of aspiration in myasthenia gravis
β Scribed by Wilma J. Koopman; Samuel Wiebe; Angela Colton-Hudson; Tas Moosa; Dean Smith; David Bach; Michael W. Nicolle
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 87 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0148-639X
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π SIMILAR VOLUMES
Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological
Four patients with myasthenia gravis presented with severe, largely isolated, bulbar and respiratory muscles weakness. Tensilon tests were positive and antiacetylcholine receptor (anti-AChR) antibody titers were negative in all patients. Only 1 patient had a greater than 10% decremental response dur
## Abstract The constrictionβdilation cycles of pupils exposed to a stationary, discrete slitβlamp beam were significantly prolonged in 25 myasthenic patients (1,060.4 Β± 45.8 msec) undergoing therapy with steroids, anticholinesterases, or both, compared to normal controls (801.9 Β± 8.6 msec) or subj
## Abstract Lymphocytes from the thymus glands of myasthenic patients and controls were characterized in terms of their percentages of Bβ and Tβcells and their ability to stimulate the proliferation of autologous peripheral blood lymphocytes. Percentages of Bβ and Tβcells were the same in the thymu
Plasma exchange before thymectomy may decrease the time on mechanical ventilation (MV) and shorten the stay in the intensive care unit (ICU) for patients with myasthenia gravis (MG). This study evaluated the effects of prethymectomy plasmapheresis. A total of 29 myasthenic patients, 18 women and 11