Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Yoshihiro Toda"'
Autor:
Aya Goji, Hiromichi Ito, Kenji Mori, Masafumi Harada, Sonoka Hisaoka, Yoshihiro Toda, Tatsuo Mori, Yoko Abe, Masahito Miyazaki, Shoji Kagami
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0169288 (2017)
Proton magnetic resonance spectroscopy (1H MRS) is a noninvasive neuroimaging method to quantify biochemical metabolites in vivo and it can serve as a powerful tool to monitor neurobiochemical profiles in the brain. Asperger's syndrome (AS) is a type
Externí odkaz:
https://doaj.org/article/56fdfefbb5024f75b19a1b539a64104c
Autor:
Tatsuo Mori, Masamune Sakamoto, Takahiro Tayama, Aya Goji, Yoshihiro Toda, Atsushi Fujita, Takeshi Mizuguchi, Maki Urushihara, Naomichi Matsumoto
Publikováno v:
Brain and Development.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3477165a51c2063d58bdcd49f26b48f
https://doi.org/10.1016/j.braindev.2023.03.001
https://doi.org/10.1016/j.braindev.2023.03.001
Autor:
Yangjun Zhang, Yoshihiro Toda
Publikováno v:
2022 IEEE-APS Topical Conference on Antennas and Propagation in Wireless Communications (APWC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f304bbb6616896e2c901003cf9b88bbe
https://doi.org/10.1109/apwc49427.2022.9899942
https://doi.org/10.1109/apwc49427.2022.9899942
Autor:
Aya Goji, Toshitaka Kawarai, Hiromichi Ito, Yoshihiro Toda, Kenji Mori, Naomichi Matsumoto, Atsushi Fujita, Tatsuo Mori
Publikováno v:
Epilepsy & Seizure. 13:45-50
Although epilepsy is a known complication in Coffin-Siris syndrome, its clinical symptoms and effective treatment methods have not been thoroughly investigated so far. Here, we present the case of a female with a 594-kb interstitial deletion at 6q25.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::426aeb89008bacbac3b6b20c66101cfd
https://doi.org/10.3805/eands.13.45
https://doi.org/10.3805/eands.13.45
Publikováno v:
Brain and Development. 42:473-476
Background Ring chromosome 20 syndrome is a rare chromosomal disorder characterized by refractory seizure, mental retardation, and behavioral problems. Although there are reports of the effective treatment of patients with antiepileptic drugs (AEDs),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a900df9baff2bf7db1130691ce238f5
https://doi.org/10.1016/j.braindev.2020.03.003
https://doi.org/10.1016/j.braindev.2020.03.003
Autor:
Shoji Kagami, Issei Imoto, Yoshihiro Toda, Mikio Sugano, Yasunobu Hayabuchi, Aya Goji, Tatsuo Mori, Akemi Ono, Ryuji Nakagawa, Keita Osumi, Kenichi Suga, Yukiko Kinoshita, Maki Urushihara
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 7, Iss 1, Pp 1-5 (2020)
Human Genome Variation, Vol 7, Iss 1, Pp 1-5 (2020)
A 1-month-old Japanese infant with cardiac rhabdomyoma was diagnosed with TSC2/PKD1 contiguous gene syndrome by targeted panel sequencing with subsequent quantitative polymerase chain reaction that revealed gross monoallelic deletion, including parts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::974d504f6e7274aa6c09fc3880c0f50d
http://europepmc.org/articles/PMC7363882
http://europepmc.org/articles/PMC7363882
Autor:
Yoko Abe, Hiromichi Ito, Aya Goji, Yoshihiro Toda, Kenji Mori, Shoji Kagami, Masahito Miyazaki, Sonoka Hisaoka, Masafumi Harada, Tatsuo Mori
Publikováno v:
Journal of Child Neurology. 32:731-739
The pathophysiology of autism spectrum disorder (ASD) is not fully understood. We used proton magnetic resonance spectroscopy to investigate metabolite concentration ratios in the anterior cingulate cortex and left cerebellum in ASD. In the ACC and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c656e227bda7b47c12f220432645d39
https://doi.org/10.1177/0883073817702981
https://doi.org/10.1177/0883073817702981
Autor:
Kaori Aibara, Toshihiro Jogamoto, Masahiro Nagai, Yoko Takami, Satoshi Tada, Mitsumasa Fukuda, Chiho Tokorodani, Rina Ando, Tatsuo Mori, Daisuke Usui, Hiroyuki Wakamoto, Kayoko Saito, Hisahide Nishio, Risako Urate, Ritsuo Nishiuchi, Tomohiro Soga, Shigehiro Nagai, Isao Saito, Reiko Arakawa, Eiichi Ishii, Yuki Yamanishi, Yoichi Kondo, Yukihiko Konishi, Mariko Eguchi, Yoshihiro Toda, Satoshi Maniwa, Aya Goji, Kentaro Okamoto, Takahiro Motoki
Publikováno v:
Braindevelopment. 42(8)
Background Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder associated with spinal motor neuron loss and characterized by generalized muscle weakness. Only a few reports exist on SMA epidemiology in Japan. Additionally, nusinersen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2ff0cea94a6cdfad05d0ceccf7b0dd7
https://pubmed.ncbi.nlm.nih.gov/32505480
https://pubmed.ncbi.nlm.nih.gov/32505480
Autor:
Nobuhiko Okamoto, Tadashi Matsumoto, Yuri Dowa, Yasutsugu Chinen, Masafumi Fukuda, Kenji Shimizu, Katsuya Tashiro, Seiji Mizuno, Kyoko Minagawa, Yoko Hiraki, Yoshihiro Toda, Osamu Shimokawa, Toshiyuki Yamamoto, Hirofumi Ohashi, Satoshi Watanabe, Seijiro Aso, Koichi Shichijo, Natsuko Shiomi, Kazunori Minatozaki, Tatsuro Kondoh, Hiroyuki Moriuchi, Keiko Shimojima, Rika Kosaki, Koh-ichiro Yoshiura
Publikováno v:
American Journal of Medical Genetics Part A. 170:908-917
Partial 1q trisomy syndrome is a rare disorder. Because unbalanced chromosomal translocations often occur with 1q trisomy, it is difficult to determine whether patient symptoms are related to 1q trisomy or other chromosomal abnormalities. The present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98ccd41c82227ca49079a5e29ad036f
https://doi.org/10.1002/ajmg.a.37496
https://doi.org/10.1002/ajmg.a.37496
Publikováno v:
Pediatrics and neonatology. 60(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e3b165cc8cdfc04519b32721b0671e
https://pubmed.ncbi.nlm.nih.gov/29884333
https://pubmed.ncbi.nlm.nih.gov/29884333