Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Fumitaka, Yoshioka"'
Publikováno v:
Brain and Development. 45:191-195
Autor:
Yukiko Nakahara, Hiroshi Ito, Hiroki Namikawa, Takashi Furukawa, Fumitaka Yoshioka, Atsushi Ogata, Jun Masuoka, Tatsuya Abe
Publikováno v:
Brain Sciences, Vol 12, Iss 4, p 473 (2022)
The development of potent and selective therapeutic approaches to glioblastoma (GBM) requires the identification of molecular pathways that critically regulate the survival and proliferation of GBM. Glioblastoma stem-like cells (GSCs) possess stem-ce
Externí odkaz:
https://doaj.org/article/9b44b1d9bcf04a1194990a1412046519
Autor:
Yuri Shojima, Atsushi Ogata, Takashi Furukawa, Hiroshi Ito, Fumitaka Yoshioka, Yukiko Nakahara, Jun Masuoka, Tatsuya Abe
Publikováno v:
Japanese Journal of Stroke. 45:250-256
Cervical Cord Compression by Aberrant Vertebral Artery Presenting with Neuralgic Pain: A Case Report
Publikováno v:
NMC Case Report Journal. 9:313-317
Autor:
Jun, Masuoka, Fumitaka, Yoshioka, Takashi, Furukawa, Motofumi, Koguchi, Hiroshi, Ito, Kohei, Inoue, Atsushi, Ogata, Yukiko, Nakahara, Tatsuya, Abe
Publikováno v:
Asian Journal of Neurosurgery. 17:156-164
True posterior communicating artery (PCoA) aneurysms are rare. Although true PCoA aneurysms have been reported to be located close to the internal carotid artery, at the middle part of PCoA, or close to the posterior cerebral artery; the best surgica
Publikováno v:
Neuro-Oncology Advances. 4:iii12-iii13
Surgery for glioma around the primary motor area (primary MA) including premotor area (PA) and supplementary motor area (SMA) is performed by general anesthesia with motor evoked potential, called asleep surgery (Asleep S) or awake surgery (Awake S).
Publikováno v:
Child's Nervous System. 37:1741-1745
Symptomatic Tarlov cysts in children are not sufficiently reported and treatment methods for Tarlov cysts are still controversial. The goal of this manuscript is to introduce a new variation of the surgical technique. We performed surgery to eliminat
Autor:
Yohane Miyata, Yonehiro Kanemura, Yuri Uchiyama, Fumihito Nozaki, Fumikatsu Nohara, Satomi Mitsuhashi, Satoshi Hada, Akihito Takeuchi, Fumihiko Ishida, Fumitaka Yoshioka, Hiroshi Terashima, Jiu Okuno-Yuguchi, Hirotomo Saitsu, Tadayuki Kumagai, Hidetoshi Taniguchi, Hiroshi Doi, Atsushi Takata, Atsuko Harada, Shinji Saitoh, Hitoshi Osaka, Eri Imagawa, Yusuke Mitani, Ayako Hattori, Yasuji Kitabatake, Koichi Tanda, Jun-ichi Takanashi, Atsushi Fujita, Hiroshi Arai, Ichiro Kuki, Makoto Kinoshita, Chikako Ogawa, Toshiyuki Itai, Yoshinori Tsurusaki, Yoshihiko Saito, Noriko Togashi, Noriko Miyake, Mazumi Miura, Hiroyuki Higashiyama, Masayasu Ohta, Yoshiichi Abe, Tetsuhiro Fukuyama, Yusuke Yachi, Tomoko Tandou, Etsuko Miyagi, Satoko Kumada, Shoko Shimokawa, Naomichi Matsumoto, Yuko Takei, Keiko Hirano, Satori Hirai, Keiichi Ozono, Yukihiro Kitai, Yuichi Takami, Mitsuo Motobayashi, Ryoko Honda, Masafumi Morimoto, Takaaki Nakano, Yuki Maki, Satoko Miyatake, Akihiko Ishiyama, Tatsuya Fukasawa, Mitsuhiro Kato, Yoshiteru Azuma, Robert Smigiel, Yushi Noguchi, Tsuyoshi Omi, Kohei Hamanaka, Naoki Ando, Masataka Taguri, Takeshi Mizuguchi, Chizuru Seiwa, Mitsuko Nakashima, Eriko Koshimizu, Shin Nabatame, Teruyuki Ishikura
Publikováno v:
Journal of Medical Genetics. 58:505-513
BackgroundVariants in the type IV collagen gene (COL4A1/2) cause early-onset cerebrovascular diseases. Most individuals are diagnosed postnatally, and the prenatal features of individuals with COL4A1/2 variants remain unclear.MethodsWe examined COL4A
Autor:
Jun Masuoka, Atsushi Ogata, Yukiko Nakahara, Tatsuya Abe, Motofumi Koguchi, Hiroshi Ito, Fumitaka Yoshioka, Hideki Izumi, Tomihiro Wakamiya, Kohei Inoue
Publikováno v:
Oncology Letters
Glioblastoma (GBM) is a malignant tumor with a high recurrence rate and has very poor prognosis in humans. The median survival is still
Autor:
Fumitaka Yoshioka, Tatsuya Abe, Atsushi Ogata, Takashi Furukawa, Kohei Inoue, Jun Masuoka, Akihiko Momozaki
Publikováno v:
Surgical Neurology International
Background: Studies on pediatric patients with moyamoya disease who presented with de novo cerebral microbleeds (CMBs) are extremely rare. Case Description: Herein, we report a 7-year-old boy with moyamoya disease who had de novo CMBs during treatmen