Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Miho Takahashi Igari"'
Autor:
Yoshiaki Kato, MD, PhD, Yoshihiro Nozaki, MD, PhD, Miho Takahashi-Igari, MD, Masato Sugano, MD, Naomasa Makita, MD, PhD, Hitoshi Horigome, MD, PhD
Publikováno v:
HeartRhythm Case Reports, Vol 8, Iss 9, Pp 636-638 (2022)
Externí odkaz:
https://doaj.org/article/e56e1fdd712b4fa79cf77440e74436f8
Autor:
Daisuke Hitaka, M.D., Tatsuo Kono, M.D., Junichi Arai, M.D., Takashi Murakami, M.D., Ph.D., Miho Takahashi-Igari, M.D., Manabu Tagawa, M.D., Kensaku Mori, M.D., Ph.D., Hidetoshi Takada, M.D., Ph.D.
Publikováno v:
Radiology Case Reports, Vol 16, Iss 11, Pp 3374-3379 (2021)
A term male infant presented with congenital hepatic arterio-veno-portal shunts. A mass-like lesion in the left lobe of the liver received blood supply from not only the umbilical vein, but also the hepatic and inferior intrahepatic arteries, communi
Externí odkaz:
https://doaj.org/article/027a3dbb3e7a48d2bd7e32cb19a556ba
Autor:
Yuka Yuhara, Takahiro Kido, Kazuo Imagawa, Yusuke Yano, Yoshihiro Nozaki, Takumi Ishiodori, Nobuyuki Ishikawa, Hideyuki Kato, Yoshiaki Kato, Miho Takahashi‐Igari, Takashi Murakami, Hitoshi Horigome, Hidetoshi Takada
Publikováno v:
Clinical Case Reports, Vol 9, Iss 4, Pp 1943-1947 (2021)
Abstract We note the risk of paradoxical embolism in patients with congenital heart defects with a right‐to‐left shunt. These patients should be managed to ensure that abdominal aortic thrombi are not overlooked when their clinical conditions cha
Externí odkaz:
https://doaj.org/article/2c931e55806c468dadeb289ebfa370ce
Autor:
Hajime Okuwaki, Yoshiaki Kato, Lisheng Lin, Yoshihiro Nozaki, Miho Takahashi‐Igari, Hitoshi Horigome
Publikováno v:
Journal of Arrhythmia, Vol 35, Iss 4, Pp 685-688 (2019)
Abstract For applying a genotype‐based treatment in neonatal long QT syndrome (LQTS), early detection of the genotype becomes an important issue. We report a case of a neonate with LQTS type 3 that presented with 2:1 atrioventricular block and unde
Externí odkaz:
https://doaj.org/article/33333e5217ce4bdbb45e5a66927420ed
Autor:
Lisheng Lin, Miho Takahashi-Igari, Yoshiaki Kato, Yoshihiro Nozaki, Mana Obata, Hiromi Hamada, Hitoshi Horigome
Publikováno v:
Case Reports in Pediatrics, Vol 2017 (2017)
We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined wit
Externí odkaz:
https://doaj.org/article/1bce3903329141ae926551d54af45723
Autor:
Takumi Ishiodori, Yusuke Yano, Yuka Yuhara, Takahiro Kido, Miho Takahashi-Igari, Hidetoshi Takada, Takashi Murakami, Yoshihiro Nozaki, Yoshiaki Kato, Nobuyuki Ishikawa, Hideyuki Kato, Kazuo Imagawa, Hitoshi Horigome
Publikováno v:
Clinical Case Reports, Vol 9, Iss 4, Pp 1943-1947 (2021)
Clinical Case Reports
Clinical Case Reports
We note the risk of paradoxical embolism in patients with congenital heart defects with a right‐to‐left shunt. These patients should be managed to ensure that abdominal aortic thrombi are not overlooked when their clinical conditions change.
Publikováno v:
Pediatrics International. 64
Autor:
Miho Takahashi-Igari, Hajime Okuwaki, Yoshiaki Kato, Yoshihiro Nozaki, Lisheng Lin, Hitoshi Horigome
Publikováno v:
Journal of Arrhythmia, Vol 35, Iss 4, Pp 685-688 (2019)
Journal of Arrhythmia
Journal of Arrhythmia
For applying a genotype‐based treatment in neonatal long QT syndrome (LQTS), early detection of the genotype becomes an important issue. We report a case of a neonate with LQTS type 3 that presented with 2:1 atrioventricular block and underwent a m
Autor:
Takashi Murakami, Nobuyuki Ishikawa, Yuji Hiramatsu, Junko Shiono, Hitoshi Horigome, Hiromi Yanagisawa, Miho Takahashi-Igari, Lisheng Lin, Yoshihiro Nozaki
Publikováno v:
Pediatric Cardiology and Cardiac Surgery. 35:127-131
Autor:
Makoto Saito, Ryo Sumazaki, Yoshiaki Kato, Yoshihiro Nozaki, Miho Takahashi-Igari, Yasuhisa Urita, Lisheng Lin, Hiromi Hamada, Akihiro Nakamura, Hitoshi Horigome
Publikováno v:
Pediatric Cardiology and Cardiac Surgery. 32:328-334