Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Yukiko Mikami"'
Autor:
Haipeng Huang, Yukiko Mikami, Kosuke Shigematsu, Nozomi Uemura, Mamiko Shinsaka, Ayaka Iwatani, Fumihito Miyake, Kazuhiko Kabe, Yasushi Takai, Masahiro Saitoh, Kazunori Baba, Hiroyuki Seki
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract Background Kagami–Ogata syndrome is also known as paternal uniparental disomy 14 and related disorders and is caused by abnormal genomic imprinting in the long arm of the chromosome 14q32.2 region. Its clinical manifestations include polyh
Externí odkaz:
https://doaj.org/article/25e9fd77595a4d679079b50e613a3c44
Autor:
Nozomi Uemura, Yasushi Takai, Yukiko Mikami, Miwa Ogasawara, Masahiro Saitoh, Kazunori Baba, Junichi Tamaru, Masaaki Hara, Hiroyuki Seki
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract Background A hydatidiform mole with a coexisting fetus is a rare condition that commonly occurs as either a partial mole with fetus or a twin pregnancy comprising a complete mole and normal fetus. In the former case, the fetus is triploid, a
Externí odkaz:
https://doaj.org/article/8a123f168aed42289e95cceba7ed013f
Autor:
Yukiko Mikami, Yasushi Takai, Mana Obata-Yasuoka, Ryo Kumagai, Hiroaki Yagyu, Kosuke Shigematsu, Haipeng Huang, Nozomi Uemura, Mamiko Shinsaka, Masahiro Saitoh, Kazunori Baba, Hiroyuki Seki
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-4 (2019)
Abstract Background 17α-Hydroxylase deficiency is a recessively inherited autosomal disease caused by mutations in the CYP17A1 gene. It is a rare disease and accounts for approximately 1% of congenital adrenal cortex hyperplasias. Inhibition of 17α
Externí odkaz:
https://doaj.org/article/32eab58559e14765bd731da6e5f6c01b
Autor:
Hirotaka Ishido, Satoshi Masutani, Yukiko Mikami, Kazunori Baba, Michitaka Fuse, Keiko Mizuta, Risa Tanaka, Kenji Sugamoto, Yoichi Iwamoto, Hideaki Senzaki
Publikováno v:
Annals of Pediatric Cardiology, Vol 12, Iss 3, Pp 336-338 (2019)
Twin-twin transfusion syndrome or related conditions affect fetal loading. We report monochorionic-diamniotic twins. Twin 1 had Ebstein anomaly with mild tricuspid regurgitation (TR) and slightly thickened tricuspid valve leaflets with plastering. Tw
Externí odkaz:
https://doaj.org/article/7ba8268a10e043718e643c9dc720aab6
Autor:
Liangcheng Wang, Yasushi Takai, Kazunori Baba, Yukiko Mikami, Masahiro Saito, Isao Horiuchi, Ryo Konno, Kenjiro Takagi, Hiroyuki Seki
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 3, Pp 374-378 (2017)
Objective: The aim of the study was to determine whether the biparietal diameter/femur length (BPD/FL) ratio can be used to detect thanatophoric dysplasia in the first trimester of pregnancy. Materials and Methods: Twenty-four reported cases of thana
Externí odkaz:
https://doaj.org/article/f334a35bc2bc42319faf1a5b2a3f613f
Autor:
Liangcheng Wang, Yukiko Mikami, Yoshihisa Ono, Shigetaka Matsunaga, Masahiro Saito, Yasushi Takai, Kazunori Baba, Hiroyuki Seki
Publikováno v:
Journal of Medical Ultrasound, Vol 24, Iss 3, Pp 121-124 (2016)
An amniotic sheet is a septation in the amniotic cavity with a perforation that allows amniotic fluid to pass through. Although the incidence of abnormal placental implantation is higher in such cases, the management recommendations remain unclear. W
Externí odkaz:
https://doaj.org/article/397009feb5104529907173a6850823a2
Autor:
Yukiko Mikami, Yasushi Takai, Sumiko Era, Yoshihisa Ono, Masahiro Saitoh, Kazunori Baba, Hiromichi Suzuki, Hiroyuki Seki
Publikováno v:
Journal of International Medical Research, Vol 46 (2018)
Objectives To evaluate home blood pressure (HBP) measurements during pregnancy and postpartum and investigate differences between singleton and twin pregnancies. Methods This prospective study involved normotensive, pregnant women who were planning t
Externí odkaz:
https://doaj.org/article/c05b823c9f26447291ed787fe15d252c
Autor:
Liangcheng Wang, Isao Horiuchi, Yukiko Mikami, Kenjiro Takagi, Tomohisa Okochi, Kohei Hamamoto, Emiko Chiba, Katsuhiko Matsuura
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 54, Iss 2, Pp 187-190 (2015)
Objective: Uterine artery embolization (UAE) is a standard method for treating postpartum hemorrhage (PPH), although uterine artery vasospasm during UAE may lead to failure of hemostasis. Here, we report our experience with a case of PPH in which the
Externí odkaz:
https://doaj.org/article/a004c3afae594e13bdf2f8261a24dfee
Publikováno v:
OBM Genetics. :1-16
Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease often resulting in more severe symptoms in affected children. The number of CTG repeats is reportedly related to congenital myotonic dystrophy 1 (CDM) severity. In this study, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e2c415759f6827af64593c684189f38
https://doi.org/10.21926/obm.genet.2301179
https://doi.org/10.21926/obm.genet.2301179
Autor:
Yoshikatsu, Suzuki, Keiichi, Matsubara, Kazushi, Watanabe, Kanji, Tanaka, Tamao, Yamamoto, Tomoyoshi, Nohira, Kazuya, Mimura, Hirotada, Suzuki, Fumiaki, Hamada, Shintarou, Makino, Keiko, Koide, Haruki, Nishizawa, Katsuhiko, Naruse, Yukiko, Mikami, Ikuno, Kawabata, Jun, Yoshimatsu, Kohta, Suzuki, Shigeru, Saito
Publikováno v:
Hypertension Research. 45:1563-1574
In the near future, hypertensive disorders of pregnancy (HDP) have been diagnosed by home blood pressure monitoring (HBPM) instead of clinic BP monitoring. A multicenter study of HBPM was performed in pregnant Japanese women in the non-high risk grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e41526086ffd63b93b0744878e72de62
https://doi.org/10.1038/s41440-022-00992-3
https://doi.org/10.1038/s41440-022-00992-3