T. Okumiya
发表
M. Koga,
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Diabetology International.
Yoshiyuki Suzuki,
S. Ishii,
H. Sakuraba,
1996
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T. Numakawa,
T. Era,
N. Fusaki,
2020,
Stem cell reports.
T. Sugiura,
H. Sakuraba,
T. Okumiya,
2003,
Molecular genetics and metabolism.
E. Uyama,
E. Uyama,
Tadashi Suzuki,
1997,
Internal medicine.
T. Sugiura,
T. Kubo,
Y. Matsumura,
2017,
Journal of cardiology.
T. Sugiura,
T. Kubo,
H. Takeuchi,
2016,
International heart journal.
M. Kameyama,
M. Koga,
T. Okumiya,
2019,
bioRxiv.
T. Iwasaka,
Seishi Nakamura,
T. Sugiura,
2005,
Chest.
T. Sugiura,
I. Nishimori,
Y. Kumon,
2010,
Microbiology and immunology.
T. Saibara,
S. Onishi,
T. Okumiya,
1990,
Journal of clinical apheresis.
T. Iwasaka,
M. Koga,
Shinya Inada,
2018,
Journal of clinical laboratory analysis (Print).
M. Kameyama,
T. Iwasaka,
M. Koga,
2019,
bioRxiv.
M. Koga,
H. Matsui,
Y. Matsumura,
2019,
Scandinavian journal of clinical and laboratory investigation.
T. Sugiura,
Y. Doi,
H. Takeuchi,
2004,
Chest.
α-Galactosidase gene mutations in Fabry disease: heterogeneous expressions of mutant enzyme proteins
Yoshiyuki Suzuki,
S. Ishii,
H. Sakuraba,
1995,
Human Genetics.
H. Fujita,
Mutsuo Takahashi,
H. Takeuchi,
2004,
Journal of Clinical Microbiology.
H. Yonekawa,
Yoshiyuki Suzuki,
Y. Matsuda,
1998,
Glycoconjugate Journal.
M. Kramer,
B. Fox,
Y. Raviv,
2012,
Respiratory medicine.
O. Migita,
T. Okuyama,
M. Kosuga,
2011,
Molecular genetics and metabolism.
M. Kameyama,
M. Koga,
T. Okumiya,
2022,
Clinical biochemistry.
Two novel mutations in the α-galactosidase gene in Japanese classical hemizygotes with Fabry disease
S. Ishii,
H. Sakuraba,
T. Okumiya,
1996,
Japanese Journal of Human Genetics.
F. Endo,
T. Okuyama,
M. Kroos,
2011,
Molecular genetics and metabolism.
F. Endo,
T. Okuyama,
M. Kroos,
2009,
Molecular genetics and metabolism.
S. Tsujino,
M. Ikekita,
T. Edmunds,
2007,
Journal of human genetics.
M. Kroos,
T. Okumiya,
A. T. van der Ploeg,
2010,
Expert opinion on medical diagnostics.
H. Sakuraba,
K. Itoh,
T. Okumiya,
1998,
Human mutation.
S. Marie,
W. Robberecht,
B. Engelen,
2012,
Human mutation.
A. Reuser,
M. Kroos,
H. Takeuchi,
2006,
Molecular genetics and metabolism.
I. Shiojima,
T. Sugiura,
N. Takahashi,
2020,
BMC Nephrology.
A. Reuser,
M. Kroos,
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2007,
Molecular genetics and metabolism.
Satoshi Ishii,
Toshihiro Takenaka,
Hitoshi Sakuraba,
1995
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S. Ishii,
Y. Suzuki,
H. Sakuraba,
1995,
Biochemical and biophysical research communications.
H. Doi,
H. Sakuraba,
T. Okumiya,
2005,
Human Genetics.
T. Fukuda,
T. Numakawa,
T. Era,
2021,
Neurobiology of Disease.
W. Pijnappel,
F. Catalano,
A. Bergsma,
2020,
European Journal of Human Genetics.
I. Shiojima,
Seishi Nakamura,
T. Sugiura,
2023,
BMC Nephrology.
I. Shiojima,
Seishi Nakamura,
T. Sugiura,
2021,
BMC Nephrology.
I. Shiojima,
Seishi Nakamura,
T. Sugiura,
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S. Hirose,
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2019,
Journal of Human Genetics.
T. Nakatani,
Yoshiaki Takemoto,
Kenji Tsuchida,
2000,
Nephron.
T. Sugiura,
T. Kubo,
Y. Doi,
2016,
Journal of cardiology.
S. Tsujino,
M. Ikekita,
T. Edmunds,
2007,
Journal of Human Genetics.
T. Saibara,
T. Okumiya,
Y. Jiao,
1998,
Diabetes Care.
T. Iwasaka,
M. Koga,
Shinya Inada,
2019,
Clinical biochemistry.
F. Endo,
S. Hirose,
Takahito Inoue,
2019,
Journal of Human Genetics.
T. Ishikawa,
H. Takeuchi,
T. Okumiya,
2004,
Diagnostic cytopathology.
H. Sakuraba,
M. Shimmoto,
K. Itoh,
1997,
Brain and Development.
I. Shiojima,
T. Sugiura,
N. Takahashi,
2020
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