Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kyoko Minagawa"'
Autor:
Naoya Kinota, Hiroshi Kodama, Taiki Moriyama, Junichi Taniguchi, Mitsunari Maruyama, Atsushi Ogasawara, Yasukazu Kako, Kaoru Kobayashi, Haruyuki Takaki, Akio Shibata, Kyoko Minagawa, Yasuhiro Takeshima, Koichiro Yamakado
Publikováno v:
Interventional Radiology. 7:17-20
Autor:
Sachi Tokunaga, Masumi Okuda, Kyoko Minagawa, Shogo Kikuchi, Naoko Taniguchi, Hideki Shimomura, Chikako Mure, Junji Mine, Tomoko Lee, Yasuhiko Tanaka, Yasuhiro Takeshima
Publikováno v:
Epilepsy & Seizure. 13:70-78
Autor:
Jun Shiraishi, Kyoko Minagawa, Hiroomi Okuyama, Naoto Urushihara, Shintaro Amae, Akiko Yokoi, Yuko Tazuke, Masahiro Hayakawa, Toshihiro Yanai, Kyoko Mochizuki, Hideshi Fujinaga, Kensuke Ohashi, Genshiro Esumi, Taizo Furukawa, Hiromu Miyake, Satoko Ohfuji
Publikováno v:
Surgery Today. 47:1001-1006
Very low birth weight infants (VLBWIs) are at risk of surgical intestinal disorders including necrotizing enterocolitis (NEC), focal intestinal perforation (FIP), and meconium-related ileus (MRI). We conducted this study to verify whether the timing
Autor:
Nobuhiko Okamoto, Tadashi Matsumoto, Yuri Dowa, Yasutsugu Chinen, Masafumi Fukuda, Kenji Shimizu, Katsuya Tashiro, Seiji Mizuno, Kyoko Minagawa, Yoko Hiraki, Yoshihiro Toda, Osamu Shimokawa, Toshiyuki Yamamoto, Hirofumi Ohashi, Satoshi Watanabe, Seijiro Aso, Koichi Shichijo, Natsuko Shiomi, Kazunori Minatozaki, Tatsuro Kondoh, Hiroyuki Moriuchi, Keiko Shimojima, Rika Kosaki, Koh-ichiro Yoshiura
Publikováno v:
American Journal of Medical Genetics Part A. 170:908-917
Partial 1q trisomy syndrome is a rare disorder. Because unbalanced chromosomal translocations often occur with 1q trisomy, it is difficult to determine whether patient symptoms are related to 1q trisomy or other chromosomal abnormalities. The present
Autor:
Kayoko Harada, Ryu Wada, Kyoko Minagawa, Kazutomo Isono, Hideaki Sawai, Takashi Takenobu, Shinji Komori, Reiichi Ishikura, Gen Nishimura, Hiroyuki Tanaka
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 24:1181-1184
Fetal three-dimensional helical computed tomography (3D-CT) has attracted attention in the diagnosis of fetal skeletal dysplasias because of limited diagnostic capabilities of standard ultrasonography to delineate the skeleton. Here we report the fir
Autor:
Reiichi Ishikura, Miyuki Shakudo, Hiroyuki Tanaka, Masayo Ogawa, Shozo Hirota, Masayuki Fujiwara, Kyoko Minagawa, Kumiko Ando, Satoshi Yamamoto, Yoshihiro Takada
Publikováno v:
Neuroradiology. 49:1033-1039
Chiari type II malformation (CMII) is one of three hindbrain malformations that display hydrocephalus. We have observed that cerebrospinal fluid (CSF) signal in the posterior fossa, which is always apparent on normal fetal MR images, is not visible i
Autor:
Hiroomi, Okuyama, Satoko, Ohfuji, Masahiro, Hayakawa, Naoto, Urushihara, Akiko, Yokoi, Hiroshi, Take, Jun, Shiraishi, Hideshi, Fujinaga, Kensuke, Ohashi, Kyoko, Minagawa, Maiko, Misaki, Satoko, Nose, Tomoaki, Taguchi
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 58(1)
Very low-birthweight (VLBW) infants (VLBWI) are at increased risk for surgical intestinal disorders including necrotizing enterocolitis (NEC), focal intestinal perforation (FIP) and meconium-related ileus (MRI). The aim of this study was to identify
Autor:
Haruyasu Ueda, Haruki Okamura, Kyoko Minagawa, Yoshiyuki Tsuji, Tomoko Hashimoto-Tamaoki, Koji Tanizawa, Koji Koyama
Publikováno v:
Cytokine. 17:164-170
Periventricular leukomalacia (PVL) is a neonatal white matter damage of the brain of pre-term infants that often leads to cerebral palsy (CP). At present, diagnosis of PVL can be done by magnetic resonance imaging (MRI) and ultrasonography only when
Autor:
Koji Tominaga, Hiroshi Mizumoto, Yoko Yoshikawa, Toshiro Hara, Kyoko Minagawa, Marie Noda, Kanako Kojima-Ishii, Kenji Ihara, Masayuki Ochiai, Tadamune Kinjo, Terumichi Matsuo, Maiko Misaki
Publikováno v:
American journal of medical genetics. Part A. (1)
Sotos syndrome (OMIM #117550) is a congenital syndrome characterized by overgrowth with advanced bone age, macrocephaly, and learning difficulties. Endocrine complications of this syndrome have not yet been fully described in previous reports. We her
Autor:
Hitoshi Yasoshima, Yasuko Matsuno, Kazunari Sakurai, Eriko Ohkubo, Kyoko Minagawa, Akira Kubota, Yasuo Nakata
Publikováno v:
Pathology international. 51(5)
We report an autopsy case of pancreatic and ectopic nesidioblastosis. A five-month-old Japanese girl was born at 35 weeks gestation, and showed clinical symptoms of hyper-insulinemic hypoglycemia before death. At autopsy a tumorous nodule was observe