Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Shinsuke Uraki"'
Autor:
Hiroshi Iwakura, Tomoyuki Takagi, Hidefumi Inaba, Asako Doi, Yoko Ueda, Shinsuke Uraki, Ken Takeshima, Yasushi Furukawa, Tatsuya Ishibashi, Shuhei Morita, Shohei Matsuno, Masahiro Nishi, Hiroto Furuta, Taka-aki Matsuoka, Takashi Akamizu
Publikováno v:
BMC Endocrine Disorders, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background The higher prevalence of thyroid dysfunction in type 1 diabetes patients has been well established, whereas it is a matter of debate whether that is also observed in type 2 diabetes patients. This study was conducted to reveal whe
Externí odkaz:
https://doaj.org/article/5fcd60eb1e6e4f04936ab071f0b8dd43
Autor:
Shuhei Morita, Tomoya Tsuji, Shohei Kishimoto, Shinsuke Uraki, Ken Takeshima, Hiroshi Iwakura, Hiroto Furuta, Masahiro Nishi, Hidefumi Inaba, Taka-aki Matsuoka
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background The global COVID-19 pandemic requires urgent development of new vaccines. Endocrinological adverse effects following the new mRNA vaccine against COVID-19 have been reported in several cases. Specific to the involvement of pituita
Externí odkaz:
https://doaj.org/article/3fb65338a3cd425281ddd1cbbb093e57
Autor:
Shohei Kishimoto, Shuhei Morita, Chiaki Kurimoto, Chie Kitahara, Tomoya Tsuji, Shinsuke Uraki, Ken Takeshima, Yasushi Furukawa, Hiroshi Iwakura, Hiroto Furuta, Masahiro Nishi, Taka-aki Matsuoka
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Background Early diagnosis of lymphoma involving the central nervous system is sometimes difficult but emergent to avoid the delay of therapeutic initiation. Pituitary insufficiencies are usually associated with lymphoma in the pituitary gla
Externí odkaz:
https://doaj.org/article/c8ccea5497ee403aa257ec4c70d6a47a
Autor:
Shuhei Morita, Tomoyuki Takagi, Hidefumi Inaba, Yasushi Furukawa, Shohei Kishimoto, Shinsuke Uraki, Naoki Shimo, Ken Takeshima, Saya Uraki, Kei Doi, Mitsuyo Imagawa, Mika Kokawa, Tomomi Konami, Hitomi Hara, Yoshihiro Hara, Emiko Sone, Hiroto Furuta, Masahiro Nishi, Asako Doi, Shinobu Tamura, Taka-aki Matsuoka
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectivesGraves’ disease (GD) has been highlighted as a possible adverse effect of the respiratory syndrome coronavirus-2 (SARS-CoV-2) vaccine. However, it is unknown if the SARS-CoV-2 vaccine disrupts thyroid autoimmunity. We aimed to present lon
Externí odkaz:
https://doaj.org/article/6ad6a17b5d254aec8771cdbe6b8fcf39
Autor:
Chie Kitahara, Shuhei Morita, Shohei Kishimoto, Shohei Matsuno, Shinsuke Uraki, Ken Takeshima, Yasushi Furukawa, Hidefumi Inaba, Hiroshi Iwakura, Hiroyuki Ariyasu, Hiroto Furuta, Masahiro Nishi, Takashi Akamizu
Publikováno v:
Journal of Diabetes Investigation, Vol 12, Iss 4, Pp 664-667 (2021)
Abstract We report the first case of intraoperatively detected euglycemic diabetic ketoacidosis (DKA) associated with sodium–glucose cotransporter 2 inhibitors during thoracic surgery. A 59‐year‐old man had a 12‐year history of type 2 diabete
Externí odkaz:
https://doaj.org/article/4d37dd9d30f14f198f73615bc4b38fa1
Autor:
Tomomi Nakao, Ken Takeshima, Hiroyuki Ariyasu, Chiaki Kurimoto, Shinsuke Uraki, Shuhei Morita, Yasushi Furukawa, Hiroshi Iwakura, Takashi Akamizu
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2020)
Thyroid storm (TS) is a life-threatening condition that may suffer thyrotoxic patients. Therapeutic plasma exchange (TPE) is a rescue approach for TS with acute hepatic failure, but it should be initiated with careful considerations. We present a 55-
Externí odkaz:
https://doaj.org/article/7a75c70865a54673944ed019955c9347
Autor:
Tatsuya Ishibashi, Shuhei Morita, Shohei Kishimoto, Shinsuke Uraki, Ken Takeshima, Yasushi Furukawa, Hidefumi Inaba, Hiroyuki Ariyasu, Hiroshi Iwakura, Hiroto Furuta, Masahiro Nishi, Feroz R Papa, Takashi Akamizu
Publikováno v:
Journal of Diabetes Investigation, Vol 11, Iss 4, Pp 801-813 (2020)
Abstract Aims/Introduction Under irremediable endoplasmic reticulum (ER) stress, hyperactivated inositol‐requiring enzyme 1α (IRE1α) triggers the terminal unfolded protein response (T‐UPR), causing crucial cell dysfunction and apoptosis. We hyp
Externí odkaz:
https://doaj.org/article/ff431383310046a381016cae5c800dcb
Autor:
Shuhei Morita, Ken Takeshima, Hiroyuki Ariyasu, Yasushi Furukawa, Shohei Kishimoto, Tomoya Tsuji, Shinsuke Uraki, Hiroyuki Mishima, Akira Kinoshita, Yuichi Takahashi, Hidefumi Inaba, Hiroshi Iwakura, Hiroto Furuta, Masahiro Nishi, Asako Doi, Shin-ichi Murata, Koh-ichiro Yoshiura, Takashi Akamizu
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background It is clinically emergent to further understand the pathological mechanism to advance therapeutic strategy for endocrine tumors. A high amount of secretory protein with tumorigenic triggers are thought to induce unfolded protein r
Externí odkaz:
https://doaj.org/article/f0bbbd831d2244148713189a93965599
Autor:
Hidefumi Inaba, Hiroyuki Ariyasu, Hiroshi Iwakura, Chiaki Kurimoto, Yoko Ueda, Shinsuke Uraki, Ken Takeshima, Yasushi Furukawa, Shuhei Morita, Yoshiaki Nakayama, Takuya Ohashi, Hidefumi Ito, Yoshiharu Nishimura, Takashi Akamizu
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Autoimmune polyglandular syndrome type 2 (APS-2) is a rare and complex clinical entity, and little is known about its etiology and progression. Case presentation A 52-year-old woman with autoimmune hepatitis (AIH) and bronchial as
Externí odkaz:
https://doaj.org/article/830e32c03bef49cea936e80ef5425ea8
Autor:
Shinsuke Uraki, Hiroto Furuta, Masakazu Miyawaki, Norihiko Matsutani, Yuko Shima, Miki Iwamoto, Shohei Matsuno, Shuhei Morita, Machi Furuta, Asako Doi, Hiroshi Iwakura, Hiroyuki Ariyasu, Masahiro Nishi, Hiroyuki Suzuki, Takashi Akamizu
Publikováno v:
Journal of Diabetes Investigation, Vol 11, Iss 2, Pp 502-505 (2020)
Abstract Neonatal diabetes is a rare disease, often caused by a monogenic abnormality. A male infant patient developed diabetic ketoacidosis at 2 months‐of‐age due to the heterozygous ABCC8 gene mutation (p.Pro1198Leu). After genetic diagnosis, i
Externí odkaz:
https://doaj.org/article/3732ee6cb89945f1b9ead2c464ff50d2