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1 Strong MJ The evidence for ALS as a multisystems disorder of limited phenotypic expression Can J Neurol Sci 2001;28:283 298 2 Swash M, Desai J Motor neuron disease: Classi cation and nomenclature ALS Other Motor Neuron Dis 2000;1:105 112 3 Traynor BJ, Codd MB, Corr B, et al Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Ailie House diagnostic criteria: A population based study Arch Neurol 2000;57:1171 1176 4 Mortara P, Chio A, Rosso MG, Leone M, Schiffer D Motor neuron disease in the province of Turin, Italy, 1966 1980: Survival analysis in an unselected population J Neurol Sci 1984;66:165 173 5 Brooks BR El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis J Neurol Sci 1994;124(Suppl):96 107 6 Siddique T, Figlewicz DA, Pericak-Vance MA, et al Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity N Engl J Med 1991;324:1381 1384 7 Bensimon G, Lacomblez L, Meininger V, et al A controlled trial of riluzole in amyotrophic lateral sclerosis N Engl J Med 1994;330:585 591 8 Ross MA, Miller RG, Berchert L, et al Toward earlier diagnosis of amyotrophic lateral sclerosis Neurology 1998;50:768 772 9 Chaudhuri KR, Crump SJ, Al-Sarraj S, et al The validation of El Escorial criteria for the diagnosis of amyotrophic lateral sclerosis: A clinical-pathological study J Neurol Sci 1995;129(Suppl):11 12

printf( "%d%d%d%d", var1, var2, var3, var4 );

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Speci c Disorders 30 Tartaglia MC, Rowe A, Findlater K, Orange JB, Grace G, Strong MJ Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis Arch Neurol 2007;64: 232 236 31 Chen R, Grand Maison F, Strong MJ, Ramsay DA, Bolton CF Motor neuron disease presenting as acute respiratory failure: A clinical and pathological study J Neurol Neurosurg Psychiatry 1996;60:455 458 32 Neary DF, Snowden JS, Gustafson L, et al Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria Neurology 1998;51:1546 1554 33 Lomen-Hoerth C, Murphy J, Langmore S, Kramer JH, Olney RK, Miller B Are amyotrophic lateral sclerosis patients cognitively normal Neurology 2003;60:1094 1097 34 Massman PJ, Sims J, Cooke N, et al Prevalence and correlates of neuropsychological de cits in amyotrophic lateral sclerosis J Neurol Neurosurg Psychiatry 1996;61:450 455 35 Ghetti G, Goebel HH Frontotemporal dementia: The posttau era Neurology 2006;67:560 561 36 Parkinson N, Ince PG, Smith MO, et al ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B) Neurology 2006;67:1074 1077 37 Daube JR Electrodiagnostic studies in amyotrophic lateral sclerosis and other motor neuron disorders Muscle Nerve 2000;23:1488 1502 38 Felice KJ, North WA Creatine kinase values in amyotrophic lateral sclerosis J Neurol Sci 1998;160:S30 S32 39 Pasinelli P, Brown RH Molecular biology of amyotrophic lateral sclerosis: Insights from genetics Nat Genet 2006;7: 710 723 40 Shaw CE, Al-Chalabi A Susceptibility genes in sporadic ALS: Separating the wheat from the chaff by international collaboration Neurology 2006;67:738 739 41 Neumann M, Sampathu DM, Kwong LK, et al Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis Science 2006;314:130 133 42 Boeve BF, Baker M, Petersen RC, et al Frontotemporal dementia and parkinsonism associated with the IVS1+IG A mutation in progranulin: A clinicopathologic study Brain 2006 E-pub Oct 9, 2006 43 Shaw PJ Molecular and cellular pathways of neurodegeneration in motor neuron disease J Neurol Neurosurg Psychiatry 2005;76:1046 1057 44 Figlewicz DA, Orrell RW The genetics of motor neuron disease ALS Other Motor Neuron Dis 2003;4:225 231 45 Fink JF Hereditary spastic paraplegia Curr Neurol Neurosci Rep 2006;6:65 76 46 Meyer T, Schwan A, Dullinger JS, et al Early-onset ALS with long-term survival associated with spastin gene mutation Neurology 2005;65:141 143 47 Dubourg O, Azzedine H, Ben Yaou R, et al The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V Neurology 206;66:1721 1726 48 Atkinson JLD, Miller GM, Krauss WF, et al Clinical and radiographic features of dural arteriovenous stula, a treatable cause of myelopathy Mayo Clin Proc 2001;76:1120 1130 49 Armon C, Daube JR Electrophysiological signs of arteriovenous malformations of the spinal cord J Neurosurg Neurol Psychiatry 1989;52:1176 1181.

Statements made up of several parts, including, possibly, other statements, are called compound statements. Compound statements obey some pretty strict rules of syntax. The if statement, for example, always looks like this:

Number and a value of 30 This will represent how many yards the player will have to run before the run is over

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