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Takahide Kokumai
Takahide Kokumai
Asahikawa Medical University
Endocrinology
Internal medicine
Medicine
Biology
Diabetes mellitus
5
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5
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0
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A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression.
2021
European Journal of Endocrinology
Shigeru Suzuki
Kumihiro Matsuo
Yoshiya Ito
Atsushi Kobayashi
Takahide Kokumai
Akiko Furuya
Osamu Ueda
Tokuo Mukai
Koichi Yano
Kenji Fujieda
Akimasa Okuno
Yusuke Tanahashi
Hiroshi Azuma
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Increase in doses of levothyroxine at the age of 3 years and above is useful for distinguishing transient and permanent congenital hypothyroidism
2020
Clinical Pediatric Endocrinology
Hinako Yamamura
Takahide Kokumai
Akiko Furuya
Shigeru Suzuki
Yusuke Tanahashi
Hiroshi Azuma
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A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation.
2020
European Journal of Medical Genetics
Shigeru Suzuki
Takahide Kokumai
Akiko Furuya
Tsunehisa Nagamori
Kumihiro Matsuo
Osamu Ueda
T. Mukai
Yoshiya Ito
Koichi Yano
Kenji Fujieda
Akimasa Okuno
Yusuke Tanahashi
Hiroshi Azuma
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Protein ingestion can significantly affect glucagon secretion along with blood urea nitrogen alteration in type 1 diabetes.
2020
Journal of Diabetes Investigation
Shigeru Suzuki
Takahide Kokumai
Yusuke Tanahashi
Hiroshi Azuma
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Sufficient increment of sulfonylurea without reintroduction of insulin ameliorates pubertal deterioration of glycaemic control in KCNJ11 neonatal diabetes treated with long-term sulfonylurea.
2020
Diabetologia
Shigeru Suzuki
Tokuo Mukai
Takahide Kokumai
Akiko Furuya
Yusuke Tanahashi
Hiroshi Azuma
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