Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Ken Ohyama"'
Autor:
Yasunobu Nosaki, Ken Ohyama, Maki Watanabe, Takamasa Yokoi, Yosuke Kobayashi, Mie Inaba, Nobuaki Wakamatsu, Katsushige Iwai
Publikováno v:
Epilepsy & Behavior Reports, Vol 14, Iss , Pp 100410- (2020)
Mowat-Wilson syndrome (MWS) is a rare genetic disorder characterized by intellectual disability, distinctive facial features, epilepsy, and multiple anomalies caused by heterozygous loss-of-function mutations in the zinc finger E-box-binding homeobox
Externí odkaz:
https://doaj.org/article/09aeddb70e954163b3bc54be20bad9cc
Publikováno v:
Case Reports in Neurological Medicine, Vol 2020 (2020)
Objective. Painful ophthalmoplegia includes nonspecific magnetic resonance imaging (MRI) manifestations and various clinical features including orbital pain and cranial nerve palsies. Treatment for painful ophthalmoplegia remains controversial. The a
Externí odkaz:
https://doaj.org/article/a92aba329f2a4263819da496dd40aed8
Publikováno v:
Internal Medicine. 62:1665-1669
Autor:
Ken, Ohyama, Haruki, Koike, Maki, Tanaka, Yasunobu, Nosaki, Takamasa, Yokoi, Katsushige, Iwai, Masahisa, Katsuno
Publikováno v:
Internal Medicine. 62:1273-1278
Objective Muscle atrophy is observed in a subset of patients with chronic inflammatory demyelinating polyneuropathy (CIDP). Its manifestation is associated with a poor functional prognosis and poor response to immunomodulatory therapies. We evaluated
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
Publikováno v:
Internal medicine (Tokyo, Japan).
IgG4-related inflammatory pseudotumor is a feature of IgG4-related disease and develops in various organs. Intracranial IgG4-related inflammatory pseudotumor is rare, and data on the clinical course and response to treatment are insufficient in the l
Autor:
Haruki Koike, Yuki Fukami, Masahiro Iijima, Ken Ohyama, Ryoji Nishi, Masahisa Katsuno, Gen Sobue
Publikováno v:
Neurology. 96:226-229
Eosinophilic granulomatosis with polyangiitis (EGPA) is one of the principal causes of vasculitic neuropathy.1 Recently, clinicopathologic differences among patients with EGPA based on their antineutrophil cytoplasmic antibody (ANCA) status have been
Autor:
Kaori Kusama, Kenichi Tanaka, Shigeru Koyano, Hiroshi Doi, Haruki Koike, Misako Kunii, Genpei Yamaura, Fumiaki Tanaka, Yuichi Higashiyama, Yosuke Miyaji, Hideto Joki, Ken Ohyama, Yoshiharu Nakae, Mikiko Tada
Publikováno v:
Internal Medicine
We herein report a 33-year-old woman who was an asymptomatic hepatitis B virus (HBV) carrier and presented with distal muscle weakness in the legs and asymmetrical paresthesia in the distal extremities. A nerve biopsy specimen revealed fibrinoid necr
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:
Maki Watanabe, Katsushige Iwai, Kazuo Nakamichi, Masayuki Saijo, Yoshiharu Miura, Takamasa Yokoi, Ken Ohyama, Yasunobu Nosaki
Publikováno v:
Internal Medicine
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system caused by reactivation of the JC virus under an immunosuppressed state. This condition carries a high risk of cryptococcal meningitis. We herein