1. Nakao, S and Takenaka, T and Maeda, M and Kodama, C and Tanaka, A and Tahara, M and Yoshida, A and Kuriyama, M and Hayashibe, H and Sakuraba, H. (1995) An atypical variant of Fabry's disease in men with left ventricular hypertrophy N Engl J Med, 333, pp. 288 - 93. [PUBMED][INFOTRIEVE][CSA]
2. Sachdev, B and Takenaka, T and Teraguchi, H and Tei, C and Lee, P and McKenna, W and Elliott, P. (2002) Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy Circulation, 105, pp. 1407 - 11. [PUBMED][INFOTRIEVE][CSA][CROSSREF]
3. Chimenti, C and Pieroni, M and Morgante, E and Antuzzi, D and Russo, A and Russo, M and Maseri, A and Frustaci, A. (2004) Prevalence of Fabry Disease in Female Patients With Late-Onset Hypertrophic Cardiomyopathy Circulation, 110, pp. 1047 - 53. [PUBMED][INFOTRIEVE][CSA][CROSSREF]
4. Desnick, R and Ioannou, Y and Eng, C.(2001) α-Galactosidase A deficiency: Fabry disease. In The metabolic and molecular basis of inherited disease. ( pp. pp 3733 - 74 ). New York : McGraw-Hill.
5. Teraguchi, H and Takenaka, T and Yoshida, A and Taguchi, S and Ninomiya, K and Yoshida, H and Horinouchi, M and Yonezawa, S and Nakao, S and Minagoe, S and Tei, S. (2004) End-stage cardiac manifestations and autopsy findings in patients with cardiac Fabry disease J Cardiol, 43, pp. 98 - 9. [PUBMED][INFOTRIEVE][CSA]