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But the rules for RSI, Stochastics, and Bollinger Bands were not as clear Just to experiment, we bought when RSI crossed below 30 and sold when it crossed above 70 For Stochastics, we used 20 and 80, although we were aware these were not designed to be actionable trades In case you were curious, Bollinger Bands had the best results, which was probably because the three-year period was so volatile and Bollinger Bands self-adapt in this type of environment.

KARK RAP, ROSENBERG RN, SCHUT LJ (eds): Advances in Neurology Vol 21 The Inherited Ataxias New York, Raven Press, 1978 KATZMAN R: Education and the prevalence of dementia and Alzheimer s disease Neurology 43:13, 1993 KENNEDY WR, ALTER M, SUNG JH: Progressive proximal spinal and bulbar muscular atrophy of late onset: A sex-linked recessive trait Neurology 18:617, 1968 KERTESZ A: Frontotemporal dementia and Pick s disease Ann Neurol 54(Suppl 5): 2003 KIERNAN JA, HUDSON AJ: Frontal lobe atrophy in motor neuron diseases Brain 117:747, 1994 KIRBY R, FOWLER C, GOSLING J, BANNISTER R: Urethrovesical dysfunction in progressive autonomic failure with multiple system atrophy J Neurol Neurosurg Psychiatry 49:554, 1986 KIRSHNER HS, TANRIDAG O, THURMAN L, WHETSELL WO JR: Progressive aphasia without dementia: Two cases with focal spongiform degeneration Ann Neurol 22:527, 1987.

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KJELLIN KG: Hereditary spastic paraplegia and retinal degeneration (Kjellin syndrome and Barnard-Scholz syndrome), in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology Vol 22 Amsterdam, North-Holland, 1975, pp 467 473 KLEIN C, BROWN R, WENNING G, et al: The cold hands sign in multiple system atrophy Mov Disord 12:514, 1997 KNOPMAN DS, MASTRI AR, FREY II, et al: Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia Neurology 40:251, 1990 KOEPPEN AH: The hereditary ataxias J Neuropathol Exp Neurol 57:531, 1998 KOLLER WC: Pharamcologic treatment of parkinsonian tremor Arch Neurol 43:126 1984 KOLODNY EH, RAGHAVAN SS: GM2-gangliosidosis hexosaminidase mutations not of the Tay-Sachs type produce unusual clinical variants Trends Neurosci 6:16, 1983 KONIGSMARK BW: Hereditary diseases of the nervous system with hearing loss, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology Vol 22 Amsterdam, North-Holland, 1975, pp 499 526.

KONIGSMARK BW, WEINER LP: The olivopontocerebellar atrophies: A review Medicine 49:227, 1970 KORF BR: The hereditary dystonias: An emerging story with a twist Ann Neurol 44:4, 1998 KOSAKA K: Diffuse Lewy body disease in Japan J Neurol 237:197, 1990 KRUGER R, VIEIRA-SAECKER AM, KUHN W, et al: Increased susceptibility to sporadic Parkinson s disease by a certain combined -synuclein/ apolipoprotein E genotype Ann Neurol 45:611, 1999 KUGELBERG E: Chronic proximal (pseudomyopathic) spinal muscular atrophy: Kugelberg-Welander syndrome, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology Vol 22 Amsterdam, North-Holland, 1975, pp 67 80 KUGELBERG E, WELANDER L: Heredofamilial juvenile muscular atrophy simulating muscular dystrophy Arch Neurol Psychiatry 5:500, 1956 KUIPERS-UPMEIJER J, DE JAGER AE, HEW JM, et al: Primary lateral sclerosis: Clinical, neurophysiological and magnetic resonance ndings J Neurol Neurosurg Psychiatr 71:615, 2001 LAITINEN LV: Leksell s posteroventral pallidotomy in the treatment of Parkinson s disease.

It is postulated that lactic acid or some other metabolite accumulates in muscles and activates pain receptors, but this is unproven The delayed pain, swelling, and tenderness that occur after sustained exercise of unconditioned muscles are evidently due to ber necrosis (Armstrong) Having listed all these causes of proximal pains, all physicians are aware that arthritic and mundane musculoskeletal complaints are more common causes of discomfort in practice..

J Neurosurg 76:53, 1992 LANCE JW, SCHWAB RS, PETERSON EA: Action tremor and the cogwheel phenomenon in Parkinson s disease Brain 86:95, 1963 LANG AE, LOZANO AM, MONTGOMERY E: Posteroventral medial pallidotomy in advanced Parkinson s disease: Second of two parts N Engl J Med 337:1036, 1997 LANTOS P: The de nition of multiple system atrophy: A review of recent developments J Neuropathol Exp Neurol 57:1099, 1998 LASKER AG, ZEE DS, HAIN TC, et al: Saccades in Huntington s disease: Initiation defects and distractibility Neurology 37:364, 1987 LA SPADA AR, WILSON EM, LUBAHN DB: Androgen receptor mutation in X-linked spinal and bulbar muscular atrophy Nature 352:77, 1991 LEBER T: Ueber hereditare und congenital angelegte Sehnervenleiden Graefes Arch Clin Exp Ophthalmol 17:249, 1871..

(189 CASES) 45 (24)a 10 (5) 2 (1) 40 (21) 66 (35) 26 (14)

A: 11 B: 17 C: 22 D: 34 E: 44

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