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SPECIFIC DISORDERS 74 Tarnopolsky M, Martin J Creatine monohydrate increases strength in patients with neuromuscular disease Neurology 1999;52(4):854 857 75 Walter MC, Lochmuller H, et al Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study Neurology 2000;54(9):1848 1850 76 Mendell JR, Kissel JT, et al Myoblast transfer in the treatment of Duchenne s muscular dystrophy N Engl J Med 1995;333(13):832 838 77 Darras BT, Francke U Myopathy in complex glycerol kinase de ciency patients is due to 3 deletions of the dystrophin gene Am J Hum Genet 1988;43(2):126 130 78 Guggenheim MA, McCabe ER, et al Glycerol kinase de ciency with neuromuscular, skeletal, and adrenal abnormalities Ann Neurol 1980;7(5):441 449 79 Seltzer WK, Angelini C, et al Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase de ciency Muscle Nerve 1989;12(4):307 313 80 Beckmann JS, Brown RH, et al 66th/67th ENMC sponsored international workshop: The limb-girdle muscular dystrophies, 26 28 March 1999, Naarden, The Netherlands Neuromuscul Disord 1999;9(6 7):436 445 81 Bushby, K Genetics and the muscular dystrophies Dev Med Child Neurol 2000;42(11):780 784 82 Bushby KM, Beckmann JS The 105th ENMC sponsored workshop: Pathogenesis in the non-sarcoglycan limbgirdle muscular dystrophies, Naarden, April 12 14, 2002 Neuromuscul Disord 2003;13(1):80 90 83 Gilchrist JM, M Pericak-Vance, et al Clinical and genetic investigation in autosomal dominant limb-girdle muscular dystrophy Neurology 1988;38(1):5 9 84 Chutkow JG, Heffner RR, Jr, et al Adult-onset autosomal dominant limb-girdle muscular dystrophy Ann Neurol 1986;20(2):240 248 85 Marconi G, Pizzi A, et al Limb girdle muscular dystrophy with autosomal dominant inheritance Acta Neurol Scand 1991;83(4):234 238 86 Hauser MA, Horrigan SK, et al Myotilin is mutated in limb girdle muscular dystrophy 1A Hum Mol Genet 2000;9(14):2141 2147 87 Fang W, Huang CC, et al Childhood-onset autosomaldominant limb-girdle muscular dystrophy with cardiac conduction block Muscle Nerve 1997;20(3):286 292 88 van der Kooi AJ, Ledderhof TM, et al A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement Ann Neurol 1996;39(5):636 642 89 Bonne G, Di MR Barletta, et al Mutations in the gene encoding lamin A/C cause autosomal dominant Emery Dreifuss muscular dystrophy Nat Genet 1999;21(3):285 288 90 Speer MC, Vance JM, et al Identi cation of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7 Am J Hum Genet 1999;64(2):556 562 91 Palenzuela L, Andreu AL, et al A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q321 322 Neurology 2003;61(3):404 406 92 Fardeau M, Eymard B, et al Chromosome 15-linked limbgirdle muscular dystrophy: Clinical phenotypes in Reunion Island and French metropolitan communities Neuromuscul Disord 1996;6(6):447 453.

if ( 0 == strncmp( "Hello", "Goodbye", 5 ) ) printf( "The strings are equal!" );

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57 Clerk AE, Rodillo, et al Characterisation of dystrophin in carriers of Duchenne muscular dystrophy J Neurol Sci 1991;102(2):197 205 58 Minetti C, Chang HW, et al Dystrophin de ciency in young girls with sporadic myopathy and normal karyotype Neurology 1991;41(8):1288 1292 59 Hyser CL, Doherty RA, et al Carrier assessment for mothers and sisters of isolated Duchenne dystrophy cases: The importance of serum enzyme determinations Neurology 1987;37(9):1476 1480 60 Hyser CL, Griggs RC, et al Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy Neurology 1987;37(1):4 10 61 Bakker E, Veenema H, et al Germinal mosaicism increases the recurrence risk for new Duchenne muscular dystrophy mutations J Med Genet 1989;26(9):553 559 62 Prior TW, Bartolo C, et al Spectrum of small mutations in the dystrophin coding region Am J Hum Genet 1995;57(1):22 33 63 Brooke MH, Fenichel GM, et al Clinical investigation of Duchenne muscular dystrophy Interesting results in a trial of prednisone Arch Neurol 1987;44(8):812 817 64 Fenichel GM, Florence JM, et al Long-term bene t from prednisone therapy in Duchenne muscular dystrophy Neurology 1991;41(12):1874 1877 65 Griggs RC, Moxley RT III, et al Prednisone in Duchenne dystrophy A randomized, controlled trial de ning the time course and dose response Clinical Investigation of Duchenne Dystrophy Group Arch Neurol 1991;48(4):383 388 66 Griggs RC, Moxley RT III, et al Duchenne dystrophy: Randomized, controlled trial of prednisone (18 months) and azathioprine (12 months) Neurology 1993;43(3 Pt 1):520 527 67 Mendell JR, Moxley RT, et al Randomized, double-blind six-month trial of prednisone in Duchenne s muscular dystrophy N Engl J Med 1989;320(24):1592 1597 68 Moxley RT III, Ashwal S, et al Practice parameter: Corticosteroid treatment of Duchenne dystrophy: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society Neurology 2005;64(1):13 20 69 Backman E, Henriksson KG Low-dose prednisolone treatment in Duchenne and Becker muscular dystrophy Neuromuscul Disord 1995;5(3):233 241 70 Connolly AM, Schierbecker J, et al High dose weekly oral prednisone improves strength in boys with Duchenne muscular dystrophy Neuromuscul Disord 2002;12(10):917 925 71 Angelini C, Pegoraro E, et al De azacort in Duchenne dystrophy: Study of long-term effect Muscle Nerve 1994; 17(4):386 391 72 Bonifati MD, Ruzza G, et al A multicenter, doubleblind, randomized trial of de azacort versus prednisone in Duchenne muscular dystrophy Muscle Nerve 2000;23(9): 1344 1347 73 Fenichel GM, Griggs RC, et al A randomized ef cacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy Neurology 2001;56(8):1075 1079.

Notice that the if succeeds only when the strings are equal. The function strcmp() is the unsafe version of strncmp() and should not be used.

create a variable called bashAmt, with a data type of Number and a value of 15 This variable will represent how much the nail will move down

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