Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Yasuhiro Hiwatani"'
Autor:
Shuhei Ogami, Jinsoo Koh, Katsuichi Miyamoto, Megumi Mori, Maiko Takahashi, Yoshiaki Nakayama, Mayumi Sakata, Yasuhiro Hiwatani, Yoshinori Kajimoto, Hiroshi Ishiguchi, Hidefumi Ito
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionAutoimmune encephalitis/encephalopathy (AE) is a complex and heterogeneous disease, making it difficult to predict the prognosis. The neutrophil-to-lymphocyte ratio (NLR) has emerged as a potential prognostic tool, but its usefulness rema
Externí odkaz:
https://doaj.org/article/9095361eec8249b9a94cf0c7edf3bbef
Autor:
Maiko Takahashi, Jinsoo Koh, Shoko Yorozu, Yoshinori Kajimoto, Yoshiaki Nakayama, Mayumi Sakata, Masaaki Yasui, Yasuhiro Hiwatani, Daniel Weintraub, Hidefumi Ito
Publikováno v:
Parkinson's Disease, Vol 2022 (2022)
Introduction. The Questionnaire for Impulsive-Compulsive Disorders in Parkinson’s Disease (PD)-Rating Scale (QUIP-RS) was developed to assess the severity of impulsive and compulsive behaviors (ICBs) in PD. We aimed to validate the Japanese version
Externí odkaz:
https://doaj.org/article/56395e25f0b342a0813dff97e38a846a
Autor:
Masaaki Yasui, Jinsoo Koh, Yoshiaki Nakayama, Mayumi Sakata, Yasuhiro Hiwatani, Hiroshi Ishiguchi, Hidefumi Ito
Publikováno v:
Journal of the neurological sciences. 444
Susceptibility-weighted imaging (SWI) was developed as a diagnostic tool for amyotrophic lateral sclerosis (ALS). However, its sensitivity and specificity are insufficient for accurate diagnosis. Herein, we investigated a new, simple evaluation metho
Publikováno v:
Neurological Sciences. 43:6583-6584
Autor:
Maiko Takahashi, Jinsoo Koh, Shoko Yorozu, Yoshinori Kajimoto, Yoshiaki Nakayama, Mayumi Sakata, Masaaki Yasui, Yasuhiro Hiwatani, Daniel Weintraub, Hidefumi Ito
Publikováno v:
Parkinson's disease. 2022
Introduction. The Questionnaire for Impulsive-Compulsive Disorders in Parkinson’s Disease (PD)-Rating Scale (QUIP-RS) was developed to assess the severity of impulsive and compulsive behaviors (ICBs) in PD. We aimed to validate the Japanese version
Autor:
Yoshiaki Nakayama, Tomohiro Donishi, Yoshiki Kaneoke, Mayumi Sakata, Masaki Terada, Ken-ya Murata, Jinsoo Koh, Yasuhiro Hiwatani, Masaaki Yasui, Hidefumi Ito, Masaya Hironishi, Takuya Ishida, Hiroshi Ishiguchi
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports
Scientific Reports
Impulsivity is a neuropsychiatric feature of Parkinson’s disease (PD). We investigated the pathophysiology of impulsivity in PD using resting-state functional magnetic resonance imaging (rs-fMRI). We investigated 45 patients with idiopathic PD and
Autor:
Shun Takahashi, Shunya Nakane, Shinya Uenishi, Satoshi Ukai, Tomikimi Tsuji, Yoshiaki Nakayama, Yasuhiro Hiwatani
Publikováno v:
Asian Journal of Psychiatry. 39:8-9
Autoimmune autonomic ganglionopathy (AAG) is a rare acquired immune-mediated disorder that leads to autonomic failure. It is sometimes complicated by mental and behavioral symptoms. We report a case of 72-year-old male with AAG who was admitted to th
Autor:
Sohei Yoshida, Keiko Iwai, Koichi Takamiya, Yasuhiro Hiwatani, Shigeki Kuzuhara, Yasumasa Kokubo, Ryo Okumura, Iori Sakurai, Yoshinori Kajimoto, Junko Kohmoto, Yuhto Iinuma, Tameko Kihira, Kazushi Okamoto, Ikuro Wakayama
Publikováno v:
Biological trace element research. 164(1)
The aim of this study was to evaluate the accumulation of transition metals in the scalp hair of amyotrophic lateral sclerosis (ALS) patients in the Koza/Kozagawa/Kushimoto (K) area (K-ALS) in the Kii Peninsula, Japan. Metal contents were measured in
Publikováno v:
Neurology. 71:1645-1647
Synovitis-acne-pustulosis-hyperostosis-osteitis (SAPHO) syndrome is characterized by multifocal aseptic osteomyelitis of an uncertain etiology. In 1987, it was first proposed as a unifying concept to describe the association between musculoskeletal d
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 14(2)
Our objective was to evaluate diaphragm thicknesses during respiration by ultrasonography, and compare with conventional measurements of respiratory functions in patients with amyotrophic lateral sclerosis (ALS). Thirty-six consecutive ALS patients a