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), incidence, 107 prevalence, 107 sex differences, 107 thymoma, 108, 109 exacerbating factors, 105, 106, 198, 199 genetic susceptibility, 109, 110 grading, 375 hospital morbidity and mortality record-keeping, 380 mortality, 105, 223 post-intervention classification, 377 psychological aspects, see Psychological aspects, myasthenia gravis remission, 93, 105 therapy status, 376 treatment, see Myasthenia gravis cri- sis; Treatment, myasthenia gravis Myasthenia gravis crisis (MGC), clinical presentation and evaluation, 225227 definition, 223 differential diagnosis, 227, 228 management, acetylcholinesterase inhibitors, 231 intravenous immunoglobulin, 232 plasmapheresis, 231, 232 trigger factor avoidance, 228, 229 ventilator weaning, 230, 231 ventilatory management, 229, 230 onset, 223 oropharyngeal dysfunction, 225, 226 outcome factors, 232, 233 precipitants and drug exacerbation, 223225 respiratory abnormalities, 225, 226 Myasthenia Gravis Foundation of America (MGFA), clinical research standards, clinical classification, 374 grading, 375 hospital morbidity and mortality, 380 post-intervention status classification, 377 therapy status, 376 thymectomy classification, 378, 379 Mycophenolate mofetil, dosing, 203 mechanism of action, 207 side effects, 203, 207 Myosin, antibodies in myasthenia gravis, 58 NCS, see Nerve conduction study Neck, myasthenia gravis symptoms, 95, 98 Needle electromyography (EMG), botulism findings, 171 electrodiagnostic strategy for sus- pected neuromuscular junc- tion defect, 172174 Lambert-Eaton syndrome findings, 171 motor unit action potentials, fibrillation potentials, 152 moment-to-moment variation, 152 short duration, low amplitude, polyphasic potentials, 152 myasthenia gravis findings, 168 Neonatal myasthenia gravis, incidence, 93 Nerve conduction study (NCS), botulism findings, 171 compound muscle action potential in neuromuscular disorders, 151 Crystals in Bone Studied by Small-Angle X-Ray-Scattering, Calcif.

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