Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Daisuke, Higeta"'
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 62, Iss 4, Pp 562-565 (2023)
Objective: Having a single coronary artery (SCA) is a rare congenital anomaly in which a single artery arises from the aorta. Although most cases of SCA are asymptomatic and incidental, its effects during the perinatal period remain unknown. Herein,
Externí odkaz:
https://doaj.org/article/ba9c49bad613494c98a17d894d441d72
Autor:
Chiaki Banzai, Akina Matsumoto, Daisuke Higeta, Yu Shinozaki, Tomomi Murata, Junji Mitsushita, Masayuki Soda
Publikováno v:
Gynecology and Minimally Invasive Therapy, Vol 12, Iss 1, Pp 48-50 (2023)
The patient was a 32-year-old woman, gravida three, para one with one prior cesarean section. She became pregnant spontaneously, but the pregnancy implanted in the isthmus of the right fallopian tube, and therefore, she underwent laparoscopic right s
Externí odkaz:
https://doaj.org/article/5cf1738d5e614bf298883d545a2aad5f
Pregnancy in hereditary sensory and autonomic neuropathy type V: A case report and literature review
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 115-117 (2022)
Objective: Hereditary sensory and autonomic neuropathies (HSANs) are a clinical heterogenous group of inherited neuropathies featuring prominent sensory and autonomic involvement. We report on the management of pregnancy and delivery in a woman with
Externí odkaz:
https://doaj.org/article/dcf4854ba5474b658ae50641f99795a3
Postpartum unscarred uterine rupture caused by placenta accreta: A case report and literature review
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1587-1590 (2021)
Key Clinical Message Our case and the literature review suggest that placenta accreta spectrum, with use of uterotonics and manual removal of placenta, could be risk factors for postpartum unscarred uterine rupture.
Externí odkaz:
https://doaj.org/article/da5035cbbefa48dd8e95bed6b4f86bea
Autor:
Mio Kanbe, Masakiyo Yatomi, Ikuo Wakamatsu, Shogo Uno, Chiharu Hanazato, Haruka Aoki-Saito, Tomomi Masuda, Koichi Yamaguchi, Norimitsu Kasahara, Yosuke Miura, Hiroaki Tsurumaki, Kenichiro Hara, Yasuhiko Koga, Noriaki Sunaga, Daisuke Higeta, Takashi Kameda, Takeshi Hisada, Toshitaka Maeno
Publikováno v:
Breathe, Vol 18, Iss 2 (2022)
Externí odkaz:
https://doaj.org/article/65cafb7599d741b5a8ad9615473df8d6
Autor:
Masayuki Soda, Chiaki Banzai, Daisuke Higeta, Tomomi Murata, Hikaru Hiraishi, Noriko Tsukagoshi
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 47:2773-2776
A patient became pregnant by in vitro fertilization and embryo transfer (IVF-ET). She had a history of laparoscopic bilateral salpingectomy and enucleation of a left ovarian tumor due to bilateral hydrosalpinx and left endometriotic cyst in primary i
Postpartum unscarred uterine rupture caused by placenta accreta: A case report and literature review
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 3, Pp 1587-1590 (2021)
Clinical Case Reports, Vol 9, Iss 3, Pp 1587-1590 (2021)
Key Clinical Message Our case and the literature review suggest that placenta accreta spectrum, with use of uterotonics and manual removal of placenta, could be risk factors for postpartum unscarred uterine rupture.
Our case and the literature r
Our case and the literature r
Autor:
Kunio Yanagisawa, Yohei Osaki, Norifumi Tsukamoto, Takuma Ishizaki, Hiroaki Shimizu, Takayuki Saitoh, Yoshiyuki Ogawa, Hiroshi Handa, Daisuke Higeta, Akihito Morita, Takashi Kameda
Publikováno v:
The Kitakanto Medical Journal. 69:227-232
Pregnancy in hereditary sensory and autonomic neuropathy type V: A case report and literature review
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 115-117 (2022)
Objective: Hereditary sensory and autonomic neuropathies (HSANs) are a clinical heterogenous group of inherited neuropathies featuring prominent sensory and autonomic involvement. We report on the management of pregnancy and delivery in a woman with
Autor:
Daisuke Higeta, Takeshi Takagi, Takashi Minegishi, Gen Nishimura, Kiyoko Sameshima, Kayoko Saito, Rie Yamaguchi
Publikováno v:
Congenital Anomalies. 58:194-197
Campomelic dysplasia is an autosomal dominant skeletal dysplasia caused by heterozygous SOX9 mutations. Most patients are sporadic due to a de novo mutation. Familial campomelic dysplasia is very rare. We report on a familial campomelic dysplasia cau