Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Tomoya Kawazoe"'
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 10, Iss , Pp 100242- (2024)
Introduction: The present study characterized the degeneration of nigrostriatal dopaminergic neurons in the early stages of parkinsonian disorders using integrative neuroimaging analysis with neuromelanin-sensitive MRI and 123I-FP-CIT dopamine transp
Externí odkaz:
https://doaj.org/article/a5eba345580d45a29e708640465c463e
Autor:
Yohei Mukai, Yoshihiko Furusawa, Yuko Morimoto, Yuka Hama, Tomoya Kawazoe, Yuji Saitoh, Takashi Sakamoto, Yuji Takahashi, Miho Murata
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 1, Iss , Pp 82-85 (2019)
Background: Patients with Parkinson's disease and related disorders (PDRD) may exhibit dropped head syndrome (DHS), which does not yet have an effective treatment. Objectives: To evaluate the effect of combining lidocaine injection into the bilateral
Externí odkaz:
https://doaj.org/article/e7ce61bcc2074ccc814a5ed7ffd3edda
Autor:
Tomoya Kawazoe, Toshiyuki Yamamoto, Aya Narita, Kousaku Ohno, Kaori Adachi, Eiji Nanba, Atsuko Noguchi, Tsutomu Takahashi, Masamitsu Maekawa, Yoshikatsu Eto, Masafumi Ogawa, Miho Murata, Yuji Takahashi
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Niemann-Pick disease type C (NPC) is a lysosomal storage disorder with severe prognosis. Disease-specific therapy is crucial to prevent disease progression; however, diagnosing NPC is quite difficult because of remarkably variable
Externí odkaz:
https://doaj.org/article/0674b543366840c7947d2e7ab6ab8408
Autor:
Takanobu Ishiguro, Takuya Konno, Norikazu Hara, Bin Zhu, Satoshi Okada, Mamoru Shibata, Reiko Saika, Takaya Kitano, Megumi Toko, Tomohisa Nezu, Yuka Hama, Tomoya Kawazoe, Ikuko Takahashi‐Iwata, Ichiro Yabe, Kota Sato, Hayato Takeda, Shintaro Toda, Jin Nishimiya, Toshiyuki Teduka, Hiroaki Nozaki, Kensaku Kasuga, Akinori Miyashita, Osamu Onodera, Takeshi Ikeuchi
Publikováno v:
European Journal of Neurology.
Autor:
Terunori Sano, Tomoya Kawazoe, Ayako Shioya, Madoka Mori‐Yoshimura, Yasushi Oya, Kazushi Maruo, Ichizo Nishino, Mikio Hoshino, Shigeo Murayama, Yuko Saito
Publikováno v:
Neuropathology. 42:104-116
Lewy body-related α-synucleinopathy (Lewy pathology) has been reported in patients with myotonic dystrophy (DM) type 1 (DM1), but no detailed report has described the prevalence and extent of its occurrence. We studied consecutive full autopsy cases
Autor:
Eiji Isozaki, Tomoya Kawazoe, Takeshi Mizuguchi, Akihiro Kawata, Ichizo Nishino, Naomichi Matsumoto, Yuichi Goto, Shinsuke Tobisawa, Hiroshi Yoshihashi, Takashi Komori, Naohiro Egawa, Kazuhito Miyamoto, Akinori Uruha, Keizo Sugaya
Publikováno v:
Internal Medicine. 61:547-552
We herein report a case of myoclonic epilepsy with ragged-red fibers (MERRF) harboring a novel variant in mitochondrial cysteine transfer RNA (MT-TC). A 68-year-old woman presented with progressive myoclonic epilepsy with optic atrophy and peripheral
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 75(1)
Functional neurological disorders differ from malingering/factitious disorders and are diagnosed based solely on careful history taking and neurological evaluation. Some clinical characteristics, including distractibility, entrainability, and variabi
Autor:
Ryo Morishima, Ryohei Norioka, Kazushi Takahashi, Yuki Nakayama, Yuri Asano, Tomoya Kawazoe, Hideki Kimura, Kota Bokuda, Toshio Shimizu
Publikováno v:
Clinical Neurophysiology. 132:2003-2011
Objective A large N20 and P25 of the median nerve somatosensory evoked potential (SEP) predicts short survival in amyotrophic lateral sclerosis (ALS). We investigated whether high frequency oscillations (HFOs) over N20 are enlarged and associated wit
Autor:
Aki Murayama, Keizo Sugaya, Makoto Hara, Tomoya Kawazoe, Shinsuke Tobisawa, Hideto Nakajima, Kazushi Takahashi
Publikováno v:
Internal medicine (Tokyo, Japan).
The coexistence of leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-like 2 (CASPR2) autoantibodies in the same individual is surprisingly often observed. We herein report the first case of LGI1 encephalitis followed by Isaacs
Autor:
Masato Okitsu, Keizo Sugaya, Yasuhiro Nakata, Tomoya Kawazoe, Jun Ikezawa, Ryoichi Okiyama, Kazushi Takahashi
Publikováno v:
Journal of the Neurological Sciences. 449:120660