1Harper PS. Myotonic dystrophy. 2nd ed. London, Philadelphia: W. B. Saunders, 1989.
2Groh WJ, Groh MR, Groh, Saha C, et al. Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1. The new England Journal of Medicine, 2008, 358 (25): 2688- 2697.
3Rakocevic Stojanovic V,Peric S, Lavrnic D, et al. Leptin and the metabolic syndrome in patients with myotonic dystrophy 1. Acta Neurol Scand, 2010,121 (2): 94-98.
4Winblad S, Lindberg C, Hansen S. Cognitive deficits and CTG repeat expansion size in classical myotonic dystrophy type 1 (DM1). Behavioral and Brain Functions, 2006,2 ( 1 ) : 16.
5Winblad S, Hellstrom P, Lindberg C, et al. Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion. J Neurol Neurosurg Psychiatry, 2006,77 (2) : 219-223.
6Laberge L, Dauvilliers Y, Begin P, et al. Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1 : To lump or split ? Neuromucular Disorder, 2009,19 ( 6 ) : 397-402.
7Ota M, Sato N, Ohya Y, et al. Relationship between diffusion tensor imaging and brain morphology in patients with myotonie dystrophy. Neurosci lett, 2006,407(3) : 234-239.
8Caramia F, Mainero C, Gragnani F, et al. Functional MRI changes in the central motor system in myotonic dystrophy type 1. Magnetic Resonance Imaging, 2010,28 (2) : 226-234.
9Brook JD, McCurrach ME, Harley HG, et al. Molecular basis of myotonic dystrophy: Expanison of a trinucleotide (CTG)repeat at the 3'end of a transcript encoding a protein kinase family member. Cell, 1992,68(4) :799-808.
10Ranum L, Day JM. Pathogenic RNA repeat:an expanding role in genetic disease. Trend Genet, 2004,20 (10) : 506-512.
