Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Reiko Neki"'
Autor:
Shinji Katsurahgi, Chizuko Kamiya, Kaoru Yamanaka, Reiko Neki, Takekazu Miyoshi, Naoko Iwanaga, Chinami Horiuchi, Hiroaki Tanaka, Jun Yoshimatsu, Koichiro Niwa, Yaemi Takagi, Takeshi Ogo, Norifumi Nakanishi, Tomoaki Ikeda
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 58, Iss 2, Pp 183-187 (2019)
Objective: The goal of the study was to clarify the risk factors for pregnancy complicated with Eisenmenger syndrome (ES). Materials and methods: A retrospective study was performed in 15 patients with ES who were managed throughout pregnancy at one
Externí odkaz:
https://doaj.org/article/b5ab0a143aec4382a6116fb325dea256
Autor:
Shinji Katsuragi, Chizuko Kamiya, Kaoru Yamanaka, Reiko Neki, Takekazu Miyoshi, Naoko Iwanaga, Chinami Horiuchi, Hiroaki Tanaka, Jun Yoshimatsu, Koichiro Niwa, Yaemi Takagi, Takeshi Ogo, Norifumi Nakanishi, Tomoaki Ikeda
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 59, Iss 1, Pp 171- (2020)
Externí odkaz:
https://doaj.org/article/fd38b7157a19438798503849762fd039
Autor:
Chizuko A. Kamiya, Wataru Shimizu, Yoshinari Kabayashi, Takekazu Miyoshi, Chinami Horiuchi, Takashi Umekawa, Kaoru Yamanaka, Reiko Neki, Shinji Katsuragi, Jun Yoshimatsu, Tomoaki Ikeda
Publikováno v:
Journal of Arrhythmia, Vol 28, Iss 6, Pp 360-363 (2012)
Andersen-Tawil syndrome (ATS), also known as long QT syndrome type 7, is a rare autosomal dominant disease caused by a KCNJ2 mutation. The characteristic triad of ATS is periodic paralysis, dysmorphic features, and ventricular arrhythmia. We describe
Externí odkaz:
https://doaj.org/article/cc539d42ccd745c680e388d604c5edab
Autor:
Takekazu Miyoshi, MD, Wataru Shimizu, MD, Takashi Noda, MD, Yoshinari Kobayashi, MD, Chizuko A. Kamiya, MD, Kaoru Yamanaka, MD, Reiko Neki, MD, Jun Yoshimatsu, MD, Shiro Kamakura, MD
Publikováno v:
Journal of Arrhythmia, Vol 30, Iss 3, Pp 201-203 (2014)
Here, we present a rare case of fetal bradyarrhythmia following magnesium sulfate therapy for preterm labor. After we switched treatment from ritodrine hydrochloride to magnesium sulfate at 25 weeks' gestation, the fetal heart rate dropped from 150 b
Externí odkaz:
https://doaj.org/article/4b199dc106b842b286a606d9257ed62f
Autor:
Reiko NEKI
Publikováno v:
Japanese Journal of Thrombosis and Hemostasis. 33:448-456
Autor:
Masayuki Ochiai, Reiko Neki, Eriko Morishita, Tomoko Adachi, Shouichi Ohga, Takao Kobayashi, Tetsuhito Kojima, Toshiyuki Miyata, Hiroko Tsuda
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 47:3008-3033
Hereditary thrombophilia is a condition in which individuals are susceptible to the formation of thrombi due to a hereditary deficiency in anticoagulant factors, antithrombin (AT), protein C (PC), or protein S (PS). Many Japanese thrombophilia patien
Autor:
Akihiro Tsuji, Toshiyuki Miyata, Akihiro Sekine, Reiko Neki, Koichi Kokame, Tsutomu Tomita, Yumi Kashima, Ryotaro Asano, Jin Ueda, Tatsuo Aoki, Takeshi Ogo
Publikováno v:
Internal medicine (Tokyo, Japan).
Antithrombin resistance (ATR) is a newly identified strong genetic predisposition to venous thromboembolism (VTE) caused by genetic variations in prothrombin with substitutions of Arg at position 596 with either Leu, Gln, or Trp. In the present repor
Autor:
Reiko Neki
Publikováno v:
Japanese Journal of Thrombosis and Hemostasis. 32:594-599
Autor:
Akihiro Tsuji, Toshiyuki Miyata, Akihiro Sekine, Reiko Neki, Koichi Kokame, Tsutomu Tomita, Yumi Kashima, Ryotaro Asano, Jin Ueda, Tatsuo Aoki, Takeshi Ogo
Publikováno v:
Internal Medicine; 2023, Vol. 62 Issue 6, p885-888, 4p
Autor:
Keiko Maruyama, Jun Yoshimatsu, Reiko Neki, Takekazu Miyoshi, Toshiyuki Miyata, Hironori Hanada, Koichi Kokame, Hisato Oku, Saiko Asahara
Publikováno v:
Thrombosis Research. 185:1-4