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BURNS RJ, BRETAG AH, BLUMBERGS PC, HARBORD MG: Benign familial disease with muscle mounding and rippling J Neurol Neurosurg Psychiatry 57:344, 1994 CELEBISOY N, COLOGLU Z, AKBABA Y, et al: Continuous muscle bre activity: A case treated with acetazolamide J Neurol Neurosurg Psychiatry 64:256, 1998 COERS C, TELERMAN-TOPPET N, DURDA J: Neurogenic benign fasciculations, pseudomyotonia, and pseudotetany Arch Neurol 38:282, 1981 CONNER JM, EVANS DA: Genetic aspects of brodysplasia ossi cans progressiva J Med Genet 19:35, 1982 DALAKAS MC, FUGII M, LI M, et al: High dose intravenous immune globulin for stiff-person syndrome N Eng J Med 345:1870, 2001 DENNY-BROWN D, FOLEY JM: Evidence of a chemical mediator in myotonia Trans Assoc Am Physicians 62:187, 1949 DENNY-BROWN D, NEVIN S: The phenomenon of myotonia Brain 64:1, 1941 DUDLEY MA, DUDLEY AW, BERNSTEIN LH, et al: Progressive neonatal rigidity: Biochemical aspects of a new familial myopathy J Neuropathol Exp Neurol 38:311, 1979 FARIELLO R, MELOFF K, MURPHY EG, et al: A case of Schwartz-Jampel syndrome with unusual muscle biopsy ndings Ann Neurol 3:93, 1978 GLASER DL, ECONOMIDES AN, WANG L, et al: In vivo somatic cell gene transfer of an engineered Noggin mutein prevents BMP4-induced heterotopic ossi cation J Bone Joint Surg Am 85A:2332, 2003 GOLDENBERG DL: Fibromyalgia syndrome and its overlap with chronic fatigue syndrome, in Dawson DM, Sabin TD (eds): Chronic Fatigue Syndrome Boston, Little, Brown, 1993, pp 75 90 GUTMANN L, GUTMANN L: Axonal channelopathies: An evolving concept in the pathogenesis of peripheral nerve disorders Neurology 47:18, 1996 HUDSON AJ, BROWN WF, GILBERT JJ: The muscular pain-fasciculation syndrome Neurology 28:1105, 1978 ISAACS H: Continuous muscle bre activity in an Indian male with additional evidence of terminal motor bre abnormality J Neurol Neurosurg Psychiatry 30:126, 1967 JUSIC A, DOGAN S, STOJANOVIC V: Hereditary persistent distal cramps J Neurol Neurosurg Psychiatry 35:379, 1972 KAKULAS BA, ADAMS RD: Diseases of Muscle: Pathological Foundations of Clinical Myology, 4th ed Philadelphia, Harper & Row, 1985 LAMBERT EH, GOLDSTEIN NP: An unusual form of myotonia Physiologist 1:51, 1957 LANCE JW, BURKE D, POLLARD J: Hyperexcitability of motor and sensory neurons in neuromyotonia Ann Neurol 5:523, 1979 LAYZER RB: Muscle pain, cramps, and fatigue, in Engel AG, FranziniArmstrong C (eds): Myology, 2nd ed New York, McGraw-Hill, 1994, pp 1754 1768 LUTSCHG J, JERUSALEM F, LUDIN HP, et al: The syndrome of continuous muscle ber activity Arch Neurol 35:198, 1978 LUTWAK L: Myositis ossi cans progressiva: Mineral, metabolic and radioactive calcium studies of the effects of hormones Am J Med 37:269, 1964 MILLS KR, EDWARDS RHT: Investigative strategies for muscle pain J Neurol Sci 58:73, 1983 MOERSCH FP, WOLTMAN HW: Progressive uctuating muscular rigidity ( stiff-man syndrome ): Report of a case and some observations in 13 other cases Mayo Clin Proc 31:421, 1956 MULEY SA, DAY JW: Autoimmune rippling muscle Neurology 61:869, 2003 NEWSOM-DAVIS J: Neuromyotonia Rev Neurol 160(5 part 1):85, 2004 NEWSOM-DAVIS J, MILLS KR: Immunological associations of acquired neuromyotonia (Isaacs syndrome) Brain 116:453, 1993.

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If you put a disk in the A drive and receive an A: is not accessible message, the drive cannot detect a floppy disk The most common reason for this error is simply that no disk has been inserted in the drive or was not inserted all the way Check to make sure that there is a disk inserted If there is, remove the disk and try pulling the metal cover back a few times to loosen it; if the drive cannot pull the cover back, it cannot access the data on the disk

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The best practices of architecting the storage served by the Exadata Storage Servers are highlighted in this chapter It is important that you understand the different ways of carving out the storage and the recommended best practices, especially when you deploy a consolidation environment and have a need to configure a shared storage grid among all workloads or a storage grid with dedicated storage pools for each workload The Exadata Storage Servers can be monitored using the command-line utilities such as the CellCLI and dcli, and the GUI-based Enterprise Manager Grid Control Console You should use Enterprise Manager and utilize its unified management and reporting capabilities for managing and monitoring the Database Machine hardware, operating systems, Oracle database software, and the Exadata Storage Server Software, all in one centralized location However, if you choose to utilize third-party monitoring software, you can integrate with the Database Machine through the SNMP interface and propagate alerts generated by the Exadata Storage Server Software, the Database Machine hardware, and even the Oracle Enterprise Manager system to the monitoring infrastructure of your choice

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