Zobrazeno 1 - 10
of 420
pro vyhledávání: '"Yukihiro, Hasegawa"'
Autor:
Kento Ikegawa, Eri Koga, Tomoyo Itonaga, Hideya Sakakibara, Masanobu Kawai, Yukihiro Hasegawa
Publikováno v:
Endocrine Journal, Vol 71, Iss 6, Pp 561-569 (2024)
Turner syndrome (TS) is associated with a high risk of fracture due to low bone mineral density (BMD). While hypogonadism is known to play a role in decreasing BMD, other factors have not been studied well. Focusing on diet, exercise, and bone metabo
Externí odkaz:
https://doaj.org/article/ff3f977af4fa4045a39c7616b9989b81
Autor:
Kento Ikegawa, Yukihiro Hasegawa
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 128-137 (2023)
X-linked hypophosphatemia (XLH) is a rare type of hereditary hypophosphatemic rickets. Patients with XLH have various symptoms that lower their QOL as defined by HAQ, RAPID3, SF36-PCS, and SF36-MCS in adult patients and SF-10 and PDCOI in pediatric p
Externí odkaz:
https://doaj.org/article/a60a672e821c47e392238d44b6eec975
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 102-109 (2023)
Background: Most patients with idiopathic growth hormone deficiency (iGHD) in childhood have normal GH stimulation test results in adulthood. The present study aimed to investigate the characteristics and possible etiology of transient iGHD. Methods:
Externí odkaz:
https://doaj.org/article/149096b04523403e857e01c289246203
Publikováno v:
Endocrines, Vol 4, Iss 1, Pp 110-116 (2023)
X-linked hypophosphatemic rickets/osteomalacia is an inherited disease caused by the loss of function in PHEX. Elevated plasma FGF23 in patients with XLH leads to hypophosphatemia. The conventional treatment for XLH, consisting of oral phosphate and
Externí odkaz:
https://doaj.org/article/d86fca23bff44c6bb430eb94c0069ab3
Autor:
Marie Mitani-Konno, Reiko Saito, Hiroko Narumi-Wakayama, Yuki Sakai, Shuichi Suzuki, Hiroyuki Satoh, Yukihiro Hasegawa
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Background and objectivesWe herein reported ten, female neonates with transient clitoral preputial edema, which was mistaken for clitoromegaly. Although it is well known that the clitoris is prominent in premature, female neonates, there are as of ye
Externí odkaz:
https://doaj.org/article/639ee09b698e49c0bcd36aa2f595b27f
Autor:
Seiji Fukumoto, Yukihiro Hasegawa
Publikováno v:
Endocrines, Vol 4, Iss 4, Pp 720-721 (2023)
Rickets and osteomalacia are associated with impaired mineralization in growth plate cartilage and the bone osteoid [...]
Externí odkaz:
https://doaj.org/article/995fa741a590432780298cf85f2c333f
Autor:
Masanobu Kawai, Yukihiro Hasegawa
Publikováno v:
Endocrines, Vol 3, Iss 3, Pp 476-487 (2022)
Turner syndrome (TS) is a chromosomal disorder characterized by a short stature and gonadal dysgenesis, the latter of which requires estrogen replacement therapy (ERT) to induce and maintain secondary sexual characteristics. Insufficient ERT is assoc
Externí odkaz:
https://doaj.org/article/d2df93cef6244237a55b1f40752508d3
Autor:
Toshihiro Tajima, Yukihiro Hasegawa
Publikováno v:
Endocrines, Vol 3, Iss 3, Pp 522-529 (2022)
The conventional treatment for X-linked hypophosphatemia (XLH), consisting of phosphorus supplementation and a biologically active form of vitamin D (alfacalcidol or calcitriol), is used to treat rickets and leg deformities and promote growth. Howeve
Externí odkaz:
https://doaj.org/article/45ae3a522d064cbd9458b2e9d82d4b19
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:
Tomoyo Itonaga, Yukihiro Hasegawa
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
21-hydroxylase deficiency (21-OHD) is the most common form of congenital adrenal hyperplasia. In most developed countries, newborn screening enables diagnosis of 21-OHD in asymptomatic patients during the neonatal period. In addition, recent advances
Externí odkaz:
https://doaj.org/article/4678b97b85804beea126d31c39fe5f79