Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Amane Araki"'
Autor:
Amane Araki, Takahiko Horiuchi, Shin-ichi Terao, Tomoyuki Kazuta, Toshihiro Endo, Ryouta Torii, Masahisa Katsuno, Takashi Ando
Publikováno v:
Internal Medicine
A 41-year-old woman presented with recurrent dizziness. After an attack of dizziness, she felt edematous sensations in her hands. However, according to photographs taken during the attack, the edema on the back of the patient’s hands and fingers ap
Autor:
Yasushi Fujimoto, Seiya Tanaka, Masahiko Yamamoto, Gen Sobue, Atsushi Hashizume, Tomoo Mano, Amane Araki, Haruhiko Banno, Hirohisa Watanabe, Noriaki Suga, Keisuke Suzuki, Masahisa Katsuno
Publikováno v:
Annals of Clinical and Translational Neurology
Objective We examined the characteristics of dysphagia in spinal and bulbar muscular atrophy, a hereditary neuromuscular disease causing weakness of limb, facial, and oropharyngeal muscles via a videofluoroscopic swallowing study, and investigated th
Autor:
Tohru Funahashi, Iichiro Shimomura, Tohru Nakagawa, Gen Sobue, Amane Araki, Hideyuki Okano, Ken Kishida, Haruhiko Banno, Keisuke Suzuki, Manabu Ohyama, Yohei Okada, Masahisa Katsuno, Yasuhiro Hijikata, Tomonori Inagaki, Noriaki Suga, Shinichiro Yamada, Atsushi Hashizume, Hideaki Nakatsuji
Publikováno v:
Journal of Neurology. 264:839-847
This study aimed to evaluate various metabolic parameters in patients with spinal and bulbar muscular atrophy (SBMA), to investigate the association between those indices and disease severity, and to explore the underlying molecular pathogenesis. We
Publikováno v:
Rinsho Shinkeigaku. 57:591-594
We report the case of a 77-year-old woman with diabetic chorea, which presented as hemiballism of the right limbs. Initial blood examination revealed that sugar and hemoglobin A1c levels were 732 mg/dl and 12.2%, respectively. Thus, a diagnosis of hy
Publikováno v:
Rinsho Shinkeigaku. 58:332-334
A 77-year-old woman with Parkinson's disease presented with left chest pain. Physical examination revealed tenderness at her second left sternocostal joint. There was no skin rash. Chest CT revealed hyperostosis of the sternocostal joint, and cervica
Autor:
Akitoshi Hara, Kazuhiro Ikumi, Shinsuke Ishigaki, Hiroshi Ishiguro, Atsushi Enomoto, Mari Yoshida, Yoko Nakamichi, Shihomi Hidaka, Takako Izumoto, Atsushi Suzuki, Gen Sobue, Amane Araki, Shin-ichi Muramatsu, Shin Tsunekawa, Mica Ohara-Imaizumi, Atsushi Hashizume, Akiko Yamamoto, Kunihiko Araki, Makoto Tominaga, Yohei Iguchi, Shinichiro Yamada, Masahisa Katsuno, Yusuke Seino, Yasunori Takayama, Kaori Kawai, Daiyu Honda, Hiroshi Arima, Yasuhiro Hijikata
TAR DNA-binding protein 43 kDa (TDP-43), encoded by TARDBP, is an RNA-binding protein, the nuclear depletion of which is the histopathological hallmark of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder affecting both upper an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39342e5740c9aeb2986831485892996c
https://europepmc.org/articles/PMC6715357/
https://europepmc.org/articles/PMC6715357/
Autor:
Hirotaka Nakanishi, Masahiko Yamamoto, Seiya Noda, Haruhiko Banno, Madoka Iida, Hiroaki Adachi, Gen Sobue, Atsushi Hashizume, Hirohisa Watanabe, Keisuke Suzuki, Masahisa Katsuno, Yasuhiro Hijikata, Amane Araki, Akihiro Hirakawa, Tomoo Mano, Tomonori Inagaki, Shinichiro Yamada
Publikováno v:
Annals of Clinical and Translational Neurology
Objective The aim of this study was to explore the pathomechanism underlying the reduction of serum creatinine (Cr) concentrations in spinal and bulbar muscular atrophy (SBMA). Methods We evaluated blood chemistries, motor function, and muscle mass m
Autor:
Atsushi, Hashizume, Masahisa, Katsuno, Keisuke, Suzuki, Haruhiko, Banno, Yu, Takeuchi, Motoshi, Kawashima, Noriaki, Suga, Tomoo, Mano, Amane, Araki, Yasuhiro, Hijikata, Akihiro, Hirakawa, Gen, Sobue, G, Sobue
Publikováno v:
Journal of neurology. 266(5)
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset, hereditary neuromuscular disease characterized by muscle atrophy, weakness, contraction fasciculation, and bulbar involvement. Although the causative gene, androgen receptor, has been ident
Autor:
Atsushi Enomoto, Gen Sobue, Shin-ichi Muramatsu, Yohei Iguchi, Akitoshi Hara, Yoko Nakamichi, Shin Tsunekawa, Atsushi Hashizume, Yasuhiro Hijikata, Yusuke Seino, Hiroshi Arima, Amane Araki, Kunihiko Araki, Daiyu Honda, Shinsuke Ishigaki, Hiroshi Ishiguro, Kazuhiro Ikumi, Shinichiro Yamada, Takako Izumoto, Kaori Kawai, Mari Yoshida, Mica Ohara-Imaizumi, Akiko Yamamoto, Masahisa Katsuno
Publikováno v:
SSRN Electronic Journal.
Nuclear depletion of TAR DNA-binding protein 43 kDa (TDP-43), encoded by TARDBP, is the histopathological hallmark of amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder affecting motor neurons. Besides motor symptoms, ALS patient
Autor:
Haruhiko Banno, Hirohisa Watanabe, Christopher Grunseich, Keisuke Suzuki, Masahisa Katsuno, Kenneth H. Fischbeck, Atsushi Hashizume, Tomoo Mano, Masahiko Yamamoto, Gen Sobue, Yasuhiro Hijikata, Noriaki Suga, Akihiro Hirakawa, Angela Kokkinis, Amane Araki
Publikováno v:
Neuromuscular Disorders. 25:554-562
We aimed to develop, validate, and evaluate a disease-specific outcome measure for SBMA: the Spinal and Bulbar Muscular Atrophy Functional Rating Scale (SBMAFRS). We examined the Japanese version (SBMAFRS-J) in 80 Japanese SBMA subjects to evaluate i