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CHAPTER 26 73 Cafferty MS, Lovelace RE, Hays AP, Servidei S, DiMauro S, Rowland LP Polyglucosan body disease Muscle Nerve 1991;14:102 107 74 Felice KJ, Grunnet ML, Rao KR, Wolfson LI Childhoodonset spinocerebellar syndrome associated with massive polyglucosan body deposition Acta Neurol Scand 1997;95:60 64 75 Fernandes J, Huijing F Branching enzyme-de ciency glycogenosis: Studies in therapy Arch Dis Child 1968;43:347 352 76 Fishbein WN, Armbrustmacher VW, Grif n JL Myoadenylate deaminase de ciency: A new disease of muscle Science 1978;200:545 548 77 McMaster KR, Powers JM, Hennigar GR, et al Nervous system involvement in type IV glycogenosis Arch Neurol 1979;103:105 111 78 Nase S, Kunse KP, Sigmund M, Schoeder JM, Shin Y, Hanrath P A new variant of type IV glycogenosis with primary cardiac manifestation and complete branching enzyme de ciency In vivo detection by heart muscle biopsy Eur Heart J 1995;16:1695 1704 79 Servidei S, Riepe RE, Langston C, et al Severe cardiopathy in branching enzyme de ciency J Pediatr 1987;111: 51 56 80 Zellweger H, Mueller S, Ionasescu V, et al Glycogenosis IV: A new cause of infantile hypotonia J Pediatr 1972;80:842 844 81 McConkie-Rosell A, Wislon C, Picolli DA, et al Clinical and laboratory ndings in four patients with the nonprogressive hepatic form of type IV glycogen storage disease J Inherit Metab Dis 1996;29:51 58 82 Lossos A, Meiner Z, Barash V, et al Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329 Ser mutation in the glucogen-branching enzyme gene Ann Neurol 1998;44:867 872 83 Ziemssen F, Sinderm E, Schroder JM, et al Novel missense mutations in the glycogen-branching enzyme gene in adult polyglucosan body disease Ann Neurol 2000;47:536 540 84 Tay SKH, Akman HO, Wendy K, et al Fatal infantile neuromuscular presentation of glycogen storage disease type IV Neuromuscul Disord 2004;14:253 260 85 Rosenthal P, Podesta L, Grier R, et al Failure of liver transplantation to diminish cardiac deposits of amylopectin and leukocyte inclusions in type IV glycogen storage disease Liver Transpl Surg 1995;1:373 376 86 Selby R, Starzl TE, Yunis E, et al Liver transplantation for type IV glycogen storage disease N Engl J Med 1991;324:39 42 87 Starzl TE, Demetris AJ, Trucco M, et al Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher s disease N Engl J Med 1993;328:745 749 88 McArdle B Myopathy due to a defect in muscle glycogen breakdown Clin Sci 1951;10:13 35 89 Vissing J, Haller RG The effect of oral sucrose on exercise tolerance in patients with McArdle s disease N Engl J Med 2003;349:2503 2509 90 Kristjansson K, Tsujino S, DiMauro S Myophosphorylase de ciency: An unusually severe form with myoglobinuria J Pediatr 1994;125:409 410.

Want to mess with AppleScript Everything you need to do just that is already on your hard drive. Look in your Applications folder for an AppleScript subfolder (that s /Applications/AppleScript in programmer language). Inside the AppleScript subfolder, you ll find an application named Script Editor that lets you create and run AppleScript scripts. To try your hand at scripting, launch TextEdit (it s also in the Applications folder), and type a few lines of text into the text editing window that appears, as shown in the following image:

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playerChoice:String; downPosition:Number = player_mc_y; upPosition:Number = player_mc_y - 100; shootCount:Number;

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