文献
1．Steare SE, Dubowitz V, Benatar A. Subclinical cardiomyopathy in Becker muscular
dystrophy. Br Heart J 1992; 68: 304-8.
2．Saito M, Kawai H, Akaike M. Adachi K, Nishida Y, Saito S. Cardiac dysfunction with
Becker muscular dystrophy. Am Heart J 1996; 132: 642-7.
3．Melacini P, Fanin M, Danieli GA, Villanova C, Martinello F, Miorin M, Freeda MP,
Miorelli M, Mostacciuolo ML, Fasoli G, Angelini C, Volta SD. Myocardial involvement is
very frequent among patients affected with subclinical Becker's muscular dystrophy.
Circulation1996; 94: 3168-3175.
4．Hayashi Y, Ikeda U, Ogawa T, Miyashita H, Sekiguchi H, Arahata K, Shimada K.
Becker type muscular dystrophy associated with hypertrophic cardiomyopathy. Am Heart
J 1994; 128:1264-6.
5．Moorman JR, Coleman RE, Packer DL, Kissulo JA, Bell J, Hettleman BD, Stajich PA
C J, Roses AD. Cardiac involvement in myotonic dystrophy. Medicine 1985: 64: 371-387.
6．Canon DS, Wyman MG, Goldreyer BN. Clinical and induced ventricular tachycardia in
a patient with myotonic dystrophy. J Am Coll Cardiol. 1984; 4: 625-8.
7．Grigg LE, Chan W, Mond HG, Vohra JK, Downey WF. Ventricular tachycardia and
sudden death in myotonic dystrophy: clinical, electrophysiologic and pathologic features.
J Am Coll Cardiol 1985; 6: 254-6.
8．Hiromasa S, Ikeda T, Kubota K, Hattori N, Coto H, Maldonado M.S., Kupersmith J.
Ventricular tachycardia and sudden death in myotonic dystrophy. Am Heart J 1988; 115:
914-5.
9．Perloff JK, Stevenson WG, Roberts NK, Cabeen W, Weiss J. Cardiac involvement in
myotonic muscular dystrophy (Steinert's disease). Am J Cardiol 1984; 54: 1074-1081 .
10．Badano L, Autore C, Fragola PV, Picelli A, Antonini G, Vichi R, Cannata D. Left
ventricular myocardial function in myotonic dystrophy. Am J Cardiol 1993; 71:987-991 .
11．Buxton J, Shelbourne P, Davies J, Jones C, Van Tongeren T, Aslanidis C, de Jong P,
Jansen G, Anvret M, Riley B, Williamson R, Johnson K. Detection of an unstable
fragment of DNA specific to individuals with myotonic dystrophy. Nature 1992; 355:
547-548.
12．Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS,
Housman DE, Shaw DJ. Expansion of an unstable DNA region and phenotypic variation in
myotonic dystorophy. Nature 1992; 355: 545-546.
13．Brook JD, McCurrach ME, Harley HG, Buckler AJ, Church D, Aburatani H, Hunter K,
Stanton VP, Thirion JP, Hudson T, Sohn R, Zemelman B, Snell RG, Rundle SA, Crow S,
Davies J, Shelbourne P, Buxton J, Jones C, Juvonen V, Johnson K, Harper PS, Shaw DJ,
Housman DE. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG)
repeat at the 3' end of a transcript encoding a protein kinase family member. Cell 1992;
68: 799-808.
14．Timchenko L, Nastainczyk W, Schneider T, Patel B, Hofmann F, Caskey CT. Full
length myotonin protein kinase (72kDa) dispalys serine kinase activity. Proc Natl Acad
Sci USA 1995; 92: 5366-70.
