Myasthenia gravis in the tenth decade
β Scribed by Lawrence H. Phillips II; Vern C. Juel
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 159 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
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
Failure to induce and maintain remission in severe exacerbations of myasthenia gravis (MG), despite optimal care, is a common problem. We evaluated the efficacy and safety of high-dose intravenous immunoglobulin (IVIg) therapy in an open-label study of 10 patients with severe generalized myasthenia