Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fumihito Miyake"'
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:
Ayaka Iwatani, Fumihito Miyake, Hirotaka Ishido, Masayo Kanai, Akio Ishiguro, Yoichi Iwamoto, Kazuhiko Kabe, Satoshi Masutani
Publikováno v:
American Journal of Perinatology Reports, Vol 09, Iss 04, Pp e357-e360 (2019)
In fetuses, the Eustachian valve directs oxygenated blood returning from the inferior vena cava into the left atrium via the foramen ovale. If too large, the Eustachian valve can restrict right ventricular inflow, as well as induce postnatal cyanosis
Externí odkaz:
https://doaj.org/article/230b7560ccdd4ee9ac1986c8672f11fd
Autor:
Hirotaka Ishido, Yoichi Iwamoto, Akio Ishiguro, Masayo Kanai, Ayaka Iwatani, Fumihito Miyake, Satoshi Masutani, Kazuhiko Kabe
Publikováno v:
AJP Reports
American Journal of Perinatology Reports, Vol 09, Iss 04, Pp e357-e360 (2019)
American Journal of Perinatology Reports, Vol 09, Iss 04, Pp e357-e360 (2019)
In fetuses, the Eustachian valve directs oxygenated blood returning from the inferior vena cava into the left atrium via the foramen ovale. If too large, the Eustachian valve can restrict right ventricular inflow, as well as induce postnatal cyanosis
Autor:
Yasushi Takai, Mamiko Shinsaka, Nozomi Uemura, Hiroyuki Seki, Haipeng Huang, Yukiko Mikami, Ayaka Iwatani, Kazuhiko Kabe, Fumihito Miyake, Kazunori Baba, Masahiro Saitoh, Kosuke Shigematsu
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Journal of Medical Case Reports
Journal of Medical Case Reports
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 polyhydramnios
Autor:
Fumihito Miyake, Ryuta Nishikomori, Yoshitaka Honda, Hideyuki Nakashimai, Kazushi Izawa, Seira Hattori, Shigeru Ohki, Toshio Heike, Yosuke Shigematsu, Tadashi Matsubayashi
Publikováno v:
Rheumatology International