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Nihon Rinsho. Japanese Journal of Clinical Medicine|September 1, 1994
[Osteoporosis in congenital disorders]M Tsuda, T SakiyamaBiochemical and Biophysical Research Communications|May 15, 1992
The primary structure of mouse saposinM Tsuda, T Sakiyama, H Endo, et al.Acta Paediatrica Japonica : Overseas Edition|June 1, 1996
A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndromeM Tsuda, T Sakiyama, M Owada, et al.Biochemical and Biophysical Research Communications|June 15, 1983
Bone marrow transplantation for Niemann-Pick miceT Sakiyama, M Tsuda, M Owada, et al.Human Genetics|December 18, 1998
A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous diseaseM Tsuda, M Kaneda, T Sakiyama, et al.Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Mini review: animal model of human lysosomal storage disease]T SakiyamaNihon Sanka Fujinka Gakkai Zasshi|April 1, 1984
[The cervical blood flow using hydrogen gas clearance method]T SakiyamaNihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1996
[Purine nucleoside phosphorylase (PNP)]T SakiyamaNihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1996
[Purine nucleoside phosphorylase (PNP) deficiency]T SakiyamaActa Paediatrica Japonica : Overseas Edition|August 8, 1998
Spectrophotometric determination of neutrophil cytochrome b558 of chronic granulomatous diseaseC Kiryu, M Kaneda, T Shiraishi, et al.Pageof 60