Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Yuichi Kawagashira"'
Autor:
Soutarou Taguchi, Hirofumi Koide, Hiroko Oiwa, Miku Hayashi, Kazuhiro Ogawa, Chihiro Ito, Koji Nakashima, Tomoko Yuasa, Akihiro Yasumoto, Hiroaki Ando, Akifumi Fujikake, Takaaki Fukuoka, Keisuke Tokui, Masayuki Izumi, Yuka Tsunoda, Yuichi Kawagashira, Yohei Okada, Jun-Ichi Niwa, Manabu Doyu
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0255274 (2021)
ObjectiveTo clarify whether antiparkinsonian drugs contribute to nocturnal sleep disturbances in patients with Parkinson's disease (PD).BackgroundAlthough the major antiparkinsonian drugs L-dopa and dopamine agonists (DAs) have been found to affect s
Externí odkaz:
https://doaj.org/article/e8ffd43dcce34cb4b784d0d96a8bc379
Autor:
Tomoko Yoshida, MD, Yoshino Ueki, MD, Tomotaka Suzuki, MD, Yuichi Kawagashira, MD, Haruki Koike, MD, Shigeru Kusumoto, MD, Shinsuke Ida, MD, Takuya Oguri, MD, Masahiro Omura, MD, Sobue, MD, Noriyuki Matsukawa, MD
Publikováno v:
eNeurologicalSci, Vol 4, Iss C, Pp 52-55 (2016)
A 50-year-old man with acute myelogenous leukemia underwent allogeneic bone-marrow transplantation (BMT). He presented with severe diarrhoea 86 days post BMT and was diagnosed with graft-versus-host disease (GVHD) based on skin and rectal biopsies. H
Externí odkaz:
https://doaj.org/article/1e26aa445dfc4d00a8b2b8a62d842524
Autor:
Haruki Koike, Ryoji Nishi, Ken Ohyama, Saori Morozumi, Yuichi Kawagashira, Soma Furukawa, Naohiro Mouri, Yuki Fukami, Masahiro Iijima, Gen Sobue, Masahisa Katsuno
Publikováno v:
Neurology and Therapy. 11:21-38
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is a systemic disorder that frequently affects the peripheral nervous system and consists of three distinct conditions: microscopic polyangiitis (MPA), granulomatosis with polyangiitis
Autor:
Ryoji Nishi, Haruki Koike, Gen Sobue, Masahiro Iijima, Yuki Fukami, Masahisa Katsuno, Yuichi Kawagashira
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 91:650-659
ObjectiveTo describe the pathological features of Guillain-Barré syndrome focusing on macrophage-associated myelin lesions.MethodsLongitudinal sections of sural nerve biopsy specimens from 11 patients with acute inflammatory demyelinating polyneurop
Autor:
Shohei Ikeda, Masahiro Iijima, Haruki Koike, Ryoji Nishi, Gen Sobue, Yuichi Kawagashira, Yuki Fukami, Masahisa Katsuno, Ken Ohyama
Publikováno v:
Neurology. 94:e1726-e1737
ObjectiveTo investigate the clinicopathologic features of eosinophilic granulomatosis with polyangiitis (EGPA)–associated neuropathy with a focus on the presence or absence of anti-neutrophil cytoplasmic antibodies (ANCAs).MethodsWe examined the cl
Autor:
Masahiro Iijima, Ryoji Nishi, Junichirou Hagita, Haruki Koike, Yuki Fukami, Hisayoshi Niwa, Masahisa Katsuno, Yuichi Kawagashira
Publikováno v:
Internal Medicine
We herein report the case of a 67-year-old man who presented with the acute onset of limb weakness. Brain magnetic resonance imaging revealed multiple abnormal-signal-intensity lesions. Steroids were administered, and the patient initially responded.
Autor:
Joe Senda, Kunihiko Araki, Yasushi Tachi, Hazuki Watanabe, Yuichi Kawagashira, Mizuki Ito, Naoki Atsuta, Masahisa Katsuno, Hirohisa Watanabe, Gen Sobue
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 21, p3017-3017, 1p
Autor:
Masahisa Katsuno, Masahiro Iijima, Haruki Koike, Ryoji Nishi, Gen Sobue, Shohei Ikeda, Yuichi Kawagashira
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 90:988-996
ObjectiveTo evaluate the clinical and pathological correlations characterising each clinical subtype of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP).MethodsWe assessed 106 consecutive patients who had CIDP fulfilling the European
Autor:
Masahiro Iijima, Haruki Koike, Yuki Fukami, Masahisa Katsuno, Yuichi Kawagashira, Ryoji Nishi, Gen Sobue
Publikováno v:
Neurology and Clinical Neuroscience. 7:166-173
Autor:
Ryoji Nishi, Gen Sobue, Shohei Ikeda, Haruki Koike, Tomohiko Nakamura, Masahiro Iijima, Yuichi Kawagashira, Masahisa Katsuno
Publikováno v:
Internal Medicine
Objective The autonomic functions of hereditary transthyretin (ATTRm) amyloidosis, traditionally referred to as familial amyloid polyneuropathy, have primarily been investigated in patients with Val30Met mutations, and information regarding non-Val30