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did pretty darn well. The returns from the magic formula strategy were far superior to the returns of the market averages. The magic formula strategy never lost money.* The magic formula strategy beat the market averages over almost every single three-year period tested. In short, the magic formula strategy achieved better results with less risk than the market averages. Though sticking with the magic formula strategy for even three years paid off incredibly well during our test period, this may not always be the case. Even superior investment strategies may take a long time to show their stuff. If an investment strategy truly makes sense, the longer the time horizon you maintain, the better your chances for ultimate success. Time horizons of 5, 10, or even 20 years are ideal. Though not easy to do, even maintaining a three- to five-year horizon for your stock market investments should give you a large advantage over most investors. It is also the minimum time frame for any meaningful comparison of the risks and results of alternative investment strategies. We now have a better understanding of just how powerful and low risk the magic formula truly is, but we still

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Figure 13-13: The Level of Detail utility (split into two parts) can specify how objects are viewed based on given thresholds.

Others have noted the importance of gratitude, either as a valued response specifically honed when confronting the finality of death, or as an emotional stance toward existence and the munificence of nature..

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distress in the banking system,37 it seems [nonetheless] plausible that regulatory changes accounted for much of the [changes] in capital ratios 38 over time.39 The high social costs associated with threats to the soundness and stability of the international banking system40 led regulators to try to achieve a higher degree of safety by requiring banks to hold a minimum amount of capital with the intention to lower the risk of bank failures. These capital ratios are, therefore, higher than what uninsured creditors41 would require and are meant to protect the economy from negative externalities caused by bank failures especially by systemic risk.42 These external effects are also often neglected when determining economically driven capital requirements.43 In spite of the fact that this regulatory view is convincing from the standpoint of ensuring the safety of banks in specific and the banking system in general, it is unclear how it is interrelated with the economically driven views of the other three stakeholder groups (as described previously). On the one hand, the discussion above indicates that regulatory capital would exceed economically driven capital requirements because (1) it does include some of the externalities and (2) in order to be binding.44 This binding, regulatory-required, minimum capital level can, therefore, in turn impose a significant cost on banks.45 On the other hand, since the regulatory view takes the perspective of an uninsured bank creditor, regulators expect to bear some of the losses before the insured depositors, who would therefore have a higher (economically driven) capital requirement than regulators.

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Middle Eastern locations as very low compensation costs, a segment of highly educated technical workers, and historical exposure to English and other European languages. 31 Egypt is making a greater push for BPO and call-center work than ITO,32 and sees itself more as a nearshore destination for Europe than as a potential market for North American clients. One of its biggest challenges, especially in developing ITO, is its small college output: at 250,000 total graduates per year, the country has less talent entering the market each year than China has new computer science graduates.33

amine and formaldehyde. The reaction may be rationalized as leading i n i t i a l l y to the adduct JA_; loss of dimethyl amine leads to the enone _12. Cyclization by means of sulfuric acid affords the indanone (J^K This last is in turn al~ kylated on carbon (14) and O-demethylated under acidic conditions. The phenol (W) thus obtained is then alkylated on oxygen by means of ethyl bromoacetate. Saponification of the ester affords indacrinone (17) .

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