Zobrazeno 1 - 10
of 577
pro vyhledávání: '"Tomonobu, Hasegawa"'
Autor:
Takeshi Munenaga, Yosuke Ichihashi, Satsuki Nakano, Hironori Shibata, Takeshi Sato, Hiroshi Asanuma, Keiko Homma, Tomonobu Hasegawa, Tomohiro Ishii
Publikováno v:
Endocrine Journal, Vol 71, Iss 10, Pp 973-978 (2024)
There have been no reports comparing neonatal external genitalia of 5α-reductase deficiency (5αRD) with those of other 46,XY differences of sex differentiation (DSD). This study enrolled 31 Japanese cases of 46,XY DSD whose external genitalia was e
Externí odkaz:
https://doaj.org/article/8537bc9373354731b5efc0e66f86d1d4
Publikováno v:
Annals of Human Biology, Vol 51, Iss 1 (2024)
AbstractBackground The high prevalence of underweight in young women has become a serious health problem in Japan. When and how young women reach a low body mass index (BMI) has not been clarified.Aim To clarify the characteristics of BMI standard de
Externí odkaz:
https://doaj.org/article/df23d766dedf47519b14a74e5368d169
Autor:
Fumiya Takahashi, Takashi Baba, Antonius Christianto, Shogo Yanai, Hyeon-Cheol Lee-Okada, Keisuke Ishiwata, Kazuhiko Nakabayashi, Kenichiro Hata, Tomohiro Ishii, Tomonobu Hasegawa, Takehiko Yokomizo, Man Ho Choi, Ken-ichirou Morohashi
Publikováno v:
Cell Reports, Vol 43, Iss 2, Pp 113715- (2024)
Summary: The zona fasciculata (zF) in the adrenal cortex contributes to multiple physiological actions through glucocorticoid synthesis. The size, proliferation, and glucocorticoid synthesis characteristics are all female biased, and sexual dimorphis
Externí odkaz:
https://doaj.org/article/9961e1b280314f7cbbce9266e2036088
Autor:
Yuki Ishinoda, Asuka Uto, Yoshifumi Yamada, Maki Okazaki, Hidetomo Asada, Seina Wakamatsu, Isao Kurihara, Hironori Shibata, Tomohiro Ishii, Tomonobu Hasegawa, Hiroo Kumagai, Akira Kasuga
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background 17α-hydroxylase deficiency (17OHD) is a rare autosomal recessive disorder. Aldosterone levels are usually low in patients with 17OHD. However, among the approximately 150 cases of 17OHD reported to date, aldosterone levels were n
Externí odkaz:
https://doaj.org/article/dbc34b9cc9fa4969baaf5beab9f52ee9
Autor:
Takeshi Sato, MD, Mikako Inokuchi, MD, PhD, Satsuki Nakano, MD, Yu Iwabuchi, MD, PhD, Tetsu Hayashida, MD, PhD, Tomohiro Ishii, MD, PhD, Tomonobu Hasegawa, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 1, Pp 91-93 (2023)
A 43-year-old woman with genetically confirmed glycogen storage disease type Ib was suspected to have left breast cancer. Fluorodeoxyglucose-positron emission tomography showed high fluorodeoxyglucose accumulation in the whole liver as well as left m
Externí odkaz:
https://doaj.org/article/435fd147dac249eaa5e6f0ec9a0c6a68
Autor:
Kotaro Narita, Hideki Muramatsu, Satoshi Narumi, Yuji Nakamura, Yusuke Okuno, Kyogo Suzuki, Motoharu Hamada, Naoya Yamaguchi, Atsushi Suzuki, Yosuke Nishio, Anna Shiraki, Ayako Yamamori, Yusuke Tsumura, Fumi Sawamura, Masahiro Kawaguchi, Manabu Wakamatsu, Shinsuke Kataoka, Kohji Kato, Hideyuki Asada, Tetsuo Kubota, Yukako Muramatsu, Hiroyuki Kidokoro, Jun Natsume, Seiji Mizuno, Tomohiko Nakata, Hidehito Inagaki, Naoko Ishihara, Takahiro Yonekawa, Akihisa Okumura, Tomoo Ogi, Seiji Kojima, Tadashi Kaname, Tomonobu Hasegawa, Shinji Saitoh, Yoshiyuki Takahashi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Recently, whole-exome sequencing (WES) has been used for genetic diagnoses of patients who remain otherwise undiagnosed. WES was performed in 177 Japanese patients with undiagnosed conditions who were referred to the Tokai regional branch of
Externí odkaz:
https://doaj.org/article/74fa295534ea4b28abbb48acc9d5d11c
Autor:
Tomohiro Ishii, Masaki Takagi, Keisuke Nagasaki, Toshio Ohara, Kentaro Miyai, Tomoki Kosho, Fumio Takada, Gen Nishimura, Tomonobu Hasegawa
Publikováno v:
Endocrines, Vol 3, Iss 3, Pp 428-432 (2022)
Hypochondroplasia is an autosomal dominant genetic disorder due to a heterozygous pathogenic variant of the FGFR3 gene. The early diagnosis of hypochondroplasia is necessary, since growth hormone is effective for improving adult height. The genetic t
Externí odkaz:
https://doaj.org/article/9f9e93223aa640cd8433b10a80d515cf
Publikováno v:
Annals of Human Biology, Vol 49, Iss 1, Pp 1-9 (2022)
Background Large datasets of detailed anthropometric measurements are scarce in children. The Japanese Standard Association 1978–1981 survey provides a rare opportunity to use high quality data from Japanese children. Aim To construct inside leg le
Externí odkaz:
https://doaj.org/article/2aaa767cd3e54271b1e8f0e2a6c156fa
Autor:
Yukihiro Hasegawa, Tomonobu Hasegawa, Mari Satoh, Kento Ikegawa, Tomoyo Itonaga, Marie Mitani-Konno, Masanobu Kawai
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Delayed and absent puberty and infertility in Turner syndrome (TS) are caused by primary hypogonadism. A majority of patients with TS who are followed at hospitals during childhood will not experience regular menstruation. In fact, almost all patient
Externí odkaz:
https://doaj.org/article/c6a2e79f36c04ccd89e88025d421dc58
Autor:
Katsuo Tao, Midori Awazu, Misa Honda, Hironori Shibata, Takayasu Mori, Shinichi Uchida, Tomonobu Hasegawa, Tomohiro Ishii
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2021)
We report a male infant with congenital nephrogenic diabetes insipidus (NDI) who presented with hypercalcemia and hyperphosphatemia since birth. Serum sodium started to increase at 39 days. Although there was no polyuria, urine osmolality was 71 mOsm
Externí odkaz:
https://doaj.org/article/921eac8fcb5645c4bf34650b59f0e0ca