Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Mitsuo, Toyoshima"'
Autor:
Yoshihiro, Maegaki, Youichi, Kurozawa, Akiko, Tamasaki, Masami, Togawa, Akiko, Tamura, Masato, Hirao, Akihisa, Nagao, Takayuki, Kouda, Takayoshi, Okada, Hiroshi, Hayashibara, Yuichiro, Harada, Makoto, Urushibara, Chitose, Sugiura, Hitoshi, Sejima, Yuji, Tanaka, Hiroko, Matsuda-Ohtahara, Takeshi, Kasai, Kazuko, Kishi, Syunsaku, Kaji, Mitsuo, Toyoshima, Susumu, Kanzaki, Kousaku, Ohno
Publikováno v:
Brain and Development. 37:478-486
Background: Early predictors of status epilepticus (SE)-associated mortality and morbidity have not been systematically studied in children, considerably impeding the identification of patients at risk. Objectives: To determine reliable early predict
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9d7f7a8faa1afd2468320fb71e46624
https://doi.org/10.1016/j.braindev.2014.08.004
https://doi.org/10.1016/j.braindev.2014.08.004
Publikováno v:
Brain and Development. 38:947-949
Lamotrigine (LTG) is an anti-epileptic drug and mood-stabilizing agent, whose adverse effects include skin rash and dizziness. Interactions with the immune system are rare, and only a few cases linking hypogammaglobulinemia to LTG treatment have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::badf6df9c740196b3bd0f260ba2434b7
https://doi.org/10.1016/j.braindev.2016.06.006
https://doi.org/10.1016/j.braindev.2016.06.006
Autor:
Junko Takita, Makiko Saitoh, Jun-ichi Takanashi, Kenjiro Kikuchi, Masahiro Kikuchi, Masashi Mizuguchi, Daisuke Nishizawa, Tomohide Goto, Masaya Kubota, Akira Kumakura, Takashi Shiihara, Hideo Yamanouchi, Shinichi Hirose, Gaku Yamanaka, Kazutaka Ikeda, Mayu Shinohara, Mitsuo Toyoshima
Publikováno v:
Neurology. 80:1571-1576
Objective: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a childhood encephalopathy following severe febrile seizures, leaving neurologic sequelae in many patients. However, its pathogenesis remains unclear. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a52996f85863fe8fc98ed59f545e20
https://doi.org/10.1212/wnl.0b013e31828f18d8
https://doi.org/10.1212/wnl.0b013e31828f18d8
Autor:
Itsuro Higuchi, Yoshihiro Maegaki, Chihiro Yonee, Mitsuo Toyoshima, Eiji Nanba, Shinsuke Maruyama, Sarah P. Young, Aya Narita, Kousaku Ohno, Yoshifumi Kawano
Publikováno v:
Brain and Development. 34:834-839
Objective: Pompe disease is an autosomal recessive disorder caused by deficiency of the lysosomal enzyme, acid alpha-glucosidase (GAA). To the best of our knowledge, no studies have reported the results of systematic and sequential CT analyses before
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae39e4537af1c1729aef100cb281b99b
https://doi.org/10.1016/j.braindev.2012.01.013
https://doi.org/10.1016/j.braindev.2012.01.013
Autor:
Chihiro Yonee, Mitsuo Toyoshima, Yoshifumi Kawano, Keiko Shimojima, Shinsuke Maruyama, Toshiyuki Yamamoto, Yoshihiro Maegaki
Publikováno v:
American Journal of Medical Genetics Part A. :1722-1726
A patient with a 47,XX,+der(22)t(11;22)(q23.3;q11.2) karyotype exhibited brisk tendon reflex and Babinski sign with suggested pyramidal sign. A three-dimensional computed tomographic reconstruction revealed a T1-T2 vertebral fusion without hemiverteb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5311d56ecd53160c93ed7898b96a21c0
https://doi.org/10.1002/ajmg.a.32762
https://doi.org/10.1002/ajmg.a.32762
Publikováno v:
Neurologia medico-chirurgica. 49:269-272
A 3-year-old girl presented with a transethmoidal meningoencephalocele manifesting as recurrent rhinorrhea. Initially, she developed meningitis, but after treatment she experienced rhinorrhea. Two months later, she again presented with rhinorrhea. Ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eccb8672c8d4959d54c4c132a51e6999
https://doi.org/10.2176/nmc.49.269
https://doi.org/10.2176/nmc.49.269
Autor:
Masayoshi, Oguri, Yoshiaki, Saito, Chisako, Fukuda, Kazuko, Kishi, Atsushi, Yokoyama, Sooyoung, Lee, Hiroyuki, Torisu, Mitsuo, Toyoshima, Hitoshi, Sejima, Shunsaku, Kaji, Shin-Ichiro, Hamano, Toru, Okanishi, Yutaka, Tomita, Yoshihiro, Maegaki
Publikováno v:
Yonago acta medica. 59(1)
To differentiate the features of electroencephalography (EEG) after status epileptics in febrile children with final diagnosis of either febrile seizure (FS) or acute encephalopathy for an early diagnosis.We retrospectively collected data from 68 chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00328095878147898eeb4ecdaf48b93c
https://pubmed.ncbi.nlm.nih.gov/27046946
https://pubmed.ncbi.nlm.nih.gov/27046946
Autor:
Yoshihiro Maegaki, Susumu Kusunoki, Atsuro Chiba, Ayumi Uchibori, Yuichi Kodama, Hiroshi Hayami, Yukitoshi Takahashi, Chihiro Yonee, Mitsuo Toyoshima, Yoshifumi Kawano
Publikováno v:
Neuropediatrics. 44:265-267
Introduction We report the case of a patient who developed symptoms of acute cerebellar ataxia (ACA) after administration of the human papilloma virus (HPV)-16/18 vaccine. Patient and Method This patient developed symptoms of ACA, including nausea, v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53fa09560ccd71e801e8e10cd9f56019
https://doi.org/10.1055/s-0033-1333873
https://doi.org/10.1055/s-0033-1333873
Autor:
Ryutaro Kira, Haruhisa Baba, Toshiro Hara, Kenji Watanabe, Yui Takada, Yoshito Ishizaki, Mitsuo Toyoshima, Masafumi Sanefuji, Hiroyuki Torisu, Daisuke Hata, Ayumi Uematsu, Sooyoung Lee, Fumio Aragaki
Publikováno v:
Journal of the Neurological Sciences. 306:91-93
Acute encephalopathy in childhood is frequently associated with common infections, especially in East Asia. Various types have been identified although many cases remain unclassified. Congenital adrenal hyperplasia (CAH) is an autosomal recessive dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed3fe3652e226c3d04c5ca1f217b2a7d
https://doi.org/10.1016/j.jns.2011.03.037
https://doi.org/10.1016/j.jns.2011.03.037
Autor:
Masayuki Itoh, Mitsuo Toyoshima, Akira Ohtake, Chitose Sugiura, Yukiko Yatsuka, Ichizo Nishino, Taro Yamazaki, Hiroyasu Iwasa, Masakazu Kohda, Hesham Montassir, Ikuo Nagata, Yoshihiro Maegaki, Kei Murayama, Kousaku Ohno, Yoshiaki Saito, Yasushi Okazaki
Publikováno v:
Braindevelopment. 37(7)
We report on the clinical, neuropathological, and genetic findings of a Japanese case with myocerebrohepatopathy spectrum (MCHS) disorder due to polymerase gamma (POLG) mutations. A girl manifested poor sucking and failure to thrive since 4 months of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2a3f2505e185aece68bac953a1950d6
https://pubmed.ncbi.nlm.nih.gov/25466440
https://pubmed.ncbi.nlm.nih.gov/25466440