Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Hiroya Nishida"'
Autor:
Yumie Tamura, Mitsumasa Fukuda, Akihiko Ishiyama, Hiroya Nishida, Hirofumi Kashii, Hideaki Mashimo, Kenji Inoue, Hiroshi Sakuma, Satoko Kumada
Publikováno v:
Epilepsy & Behavior Reports, Vol 27, Iss , Pp 100704- (2024)
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis in children often requires early immunosuppressive therapy before antibody detection. While various electroencephalogram (EEG) patterns, including extreme delta brushes (EDBs), have been reporte
Externí odkaz:
https://doaj.org/article/e1c769e8e9404849885cdeaca4641b2c
Autor:
Kuniko Kohyama, Hiroya Nishida, Kimihiko Kaneko, Tatsuro Misu, Ichiro Nakashima, Hiroshi Sakuma
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
BackgroundThe autoantibody to myelin oligodendrocyte glycoprotein (MOG), a component of the central nervous system myelin, has been identified in a subset of demyelinating diseases. However, there is no convincing evidence to support the direct patho
Externí odkaz:
https://doaj.org/article/a63c5e6d32f44a16b07631de153f4c0f
Autor:
Atsuko Arisaka, Mitsuko Nakashima, Satoko Kumada, Kenji Inoue, Hiroya Nishida, Hideaki Mashimo, Hirofumi Kashii, Mitsuhiro Kato, Koichi Maruyama, Akihisa Okumura, Hirotomo Saitsu, Naomichi Matsumoto, Mitsumasa Fukuda
Publikováno v:
Epilepsy & Behavior Reports, Vol 15, Iss , Pp 100417- (2021)
Epileptic-dyskinetic encephalopathies are rare epilepsies characterized by early-onset epileptic encephalopathies (EOEEs) with involuntary movement. Herein, we investigated the impact of gene variants in epileptic-dyskinetic encephalopathies. Four in
Externí odkaz:
https://doaj.org/article/5aa5f75829aa4b3ab1081303d2ac18bb
Autor:
Satoko Kumada, Kenji Inoue, Takashi Komori, Hideaki Mashimo, Keisuke Takai, Harushi Mori, Mitsumasa Fukuda, Hiromi Suzuki, Hiroya Nishida, Michiharu Morino, Yasuhiro Nakata, Atsuko Arisaka
Publikováno v:
Brain and Development. 42:675-679
Aggressive immunosuppressive therapies have been proposed to treat primary angiitis of the central nervous system (PACNS). Here, we report the first successfully stabilized case of childhood, small-vessel PACNS with intravenous immunoglobulin (IVIG)
Autor:
Mari Yoshida, Teppei Komatsu, Monika Bradl, Kiyotaka Nakamagoe, Tatsuro Misu, Ichiro Nakashima, Masashi Aoki, Hiroshi Kuroda, Kazuo Fujihara, Koichi Narikawa, Hiroyoshi Suzuki, Toshimasa Ikeda, Hans Lassmann, Hiroya Nishida, Kimihiko Kaneko, Takashi Komori, Morinobu Seki, Yoshiki Takai, Shuhei Nishiyama, Hirohiko Ono, Norio Chihara, Satoko Tsuchida, Toshiyuki Takahashi
Publikováno v:
Brain. 143:1431-1446
Conformation-sensitive antibodies against myelin oligodendrocyte glycoprotein (MOG) are detectable in patients with optic neuritis, myelitis, opticomyelitis, acute or multiphasic disseminated encephalomyelitis (ADEM/MDEM) and brainstem/cerebral corti
Autor:
Hiroaki Hisakawa, Rie Miyata, Kohsuke Imai, Naoyuki Tanuma, Setsuko Hasegawa, Yohane Miyata, Akio Fujine, Kenichi Kashimada, Masatoshi Takagi, Takatoshi Hosokawa, Ayako Kashimada, Atsumi Tsuji-Hosokawa, Satoko Kumada, Yuji Sugawara, Tomoko Mizuno, Mitsugu Uematsu, Kengo Moriyama, Masaharu Hayashi, Shuki Mizutani, Takeshi Hasegawa, Tomohiro Morio, Hideaki Mashimo, Hiroshi Sakuma, Ikuko Shirai, Hiroya Nishida
Publikováno v:
Pediatric Neurology. 100:60-66
Background Ataxia telangiectasia is an autosomal recessive disorder characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy. Quality of life is severely impaired by neurological symptoms. However, curati
Autor:
Hiroya Nishida, Mitsuhiro Kato, Yukihide Momozawa, Yu-ichi Goto, Michiaki Kubo, Sayaka Ohta, Aritoshi Iida, Kan Takahashi, Jun Natsume, Kazuyuki Nakamura, Ken Inoue, Chikashi Terao, Naomichi Matsumoto, Yoichiro Kamatani, Kyoko Hoshino, Yasuo Hachiya, Eiji Nakagawa, Rie Miyata, Shunichi Kosugi, Eri Takeshita, Akihiko Ishiyama, Yoshiyuki Takahashi, Chihiro Abe-Hatano, Masayuki Sasaki, Haruko Sakamoto, Keiko Ishikawa, Mariko Okubo, Chie Murakami, Masaya Kubota
Publikováno v:
American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, 2021, 185 (5), pp.1468-1480. ⟨10.1002/ajmg.a.62138⟩
American Journal of Medical Genetics. Part a
American Journal of Medical Genetics Part A, 2021, 185 (5), pp.1468-1480. ⟨10.1002/ajmg.a.62138⟩
American Journal of Medical Genetics. Part a
Intellectual disability (ID) is characterized by significant limitations in both intellectual functioning and adaptive behaviors, originating before the age of 18 years. However, the genetic etiologies of ID are still incompletely elucidated due to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cff5fca248e02ff7020eb6a509eee5a6
https://hal.science/hal-03842199
https://hal.science/hal-03842199
Autor:
Ryo Chikuchi, Kazuhiro Iwama, Shuichi Ito, Ryuta Tanaka, Hiroya Nishida, Hirokazu Oguni, Shun Nagamine, Hidehiro Shibayama, Akiko Sekine, Satoko Kumada, Naomichi Matsumoto, M. Shichiji, Atsushi Takata, Yoshio Ikeda, Satoko Miyatake, Susumu Ito, Yuichi Oka, Toshiyuki Yamamoto, Hisayoshi Niwa, Noriko Miyake, Takeshi Yoshida, Takeshi Mizuguchi, Mitsuko Nakashima, Tomonari Awaya, Hirotomo Saitsu, Jun-ichi Takanashi
Publikováno v:
Clinical Genetics. 92:180-187
Background Leukoencephalopathy with brain calcifications and cysts (LCC) is neuroradiologically characterized by leukoencephalopathy, intracranial calcification, and cysts. Coats plus syndrome is also characterized by the same neuroradiological findi
Autor:
Hirotomo Saitsu, Hiroya Nishida, Satoko Kumada, Naomichi Matsumoto, Hideaki Mashimo, Kenji Inoue, Mitsuhiro Kato, Akihisa Okumura, Atsuko Arisaka, Mitsuko Nakashima, Koichi Maruyama, Hirofumi Kashii, Mitsumasa Fukuda
Publikováno v:
Epilepsy & Behavior Reports, Vol 15, Iss, Pp 100417-(2021)
Epilepsy & Behavior Reports
Epilepsy & Behavior Reports
Highlights • Epileptic-dyskinetic encephalopathies are rare epileptic disorders characterized by EOEE with involuntary movement. • The presence of involuntary movements in patients with EOEE caused by gene variants may be a key diagnostic symptom
Autor:
Hiroya Nishida, Kuniko Kohyama, Satoko Kumada, Jun-ichi Takanashi, Akihisa Okumura, Asako Horino, Kengo Moriyama, Hiroshi Sakuma, Nishida, Hiroya, Kohyama, Kuniko, Kumada, Satoko, Takanashi, Jun-Ichi, Okumura, Akihisa, Horino, Asako, Moriyama, Kengo, Sakuma, Hiroshi
Publikováno v:
Neurology; 4/20/2021, Vol. 96 Issue 16, pe2070-e2077, 8p