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Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Fabry disease (alpha-galactosidase deficiency)]T Okumiya, H SakurabaRinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1997
[alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)]T Okumiya, T Takata, M Sasaki, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|August 1, 1989
[A colorimetric method for determination of delta-bilirubin in serum using bilirubin oxidase (Trachyderma tsunodae)]K Umaji, T Okumiya, K Park, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|February 1, 1992
[Clinical usefulness of measurement of creatine contents in human erythrocytes as an index of erythropoiesis]T Okumiya, T Kageoka, E Hashimoto, et al.Biochemical and Biophysical Research Communications|March 27, 1996
Aggregation of the inactive form of human alpha-galactosidase in the endoplasmic reticulumS Ishii, R Kase, T Okumiya, et al.Diabetes Care|October 17, 1998
Abnormally decreased HbA1c can be assessed with erythrocyte creatine in patients with a shortened erythrocyte ageY Jiao, T Okumiya, T Saibara, et al.Clinical Biochemistry|August 28, 2001
Erythrocyte creatine as a marker of excessive erythrocyte destruction due to hypersplenism in patients with liver cirrhosisY F Jiao, T Okumiya, T Saibara, et al.The Japanese Journal of Human Genetics|September 1, 1996
Two novel mutations in the alpha-galactosidase gene in Japanese classical hemizygotes with Fabry diseaseT Okumiya, T Takenaka, S Ishii, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|April 1, 1992
[A study on creatine uptake into human erythrocytes: relation to erythrocyte aging]T Okumiya, T Kageoka, E Hashimoto, et al.Human Genetics|May 1, 1995
Alpha-galactosidase gene mutations in Fabry disease: heterogeneous expressions of mutant enzyme proteinsT Okumiya, S Ishii, R Kase, et al.Pageof 2