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of 5
pro vyhledávání: '"Yoichi Kanatsuka"'
Autor:
Takashi Jono, Shigeki Yamaguchi, Takeshi Ito, Mei Sasaki, Yoichi Kanatsuka, Ryuichiro Hayashi
Publikováno v:
Rinsho shinkeigaku = Clinical neurology.
An 80-year-old woman presented with subacute right lower limb pain and bilateral lower limb weakness. MRI of the spine showed marked cauda equina enlargement with contrast enhancement. Cerebrospinal fluid (CSF) examination showed elevated cell count,
Autor:
Shiori Asano, Shigeki Yamaguchi, Makiko Inaoka, Yoichi Kanatsuka, Izumi Mori, Kensuke Nakazawa
Publikováno v:
Rinsho Shinkeigaku. 60:795-798
A 37-year-old man who had been on bromvalerylurea (BU) medication for 11 years at a maximum dose of 2,400 mg per day for headache therapy was admitted to our hospital due to gait disturbance. He had weight loss and exanthema all over his body. Cognit
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 45:1948-1951
The present report describes a case of anti-Hu antibody-mediated encephalopathy associated with ovarian cancer. The patient developed paraneoplastic neurologic syndromes (PNS) during the course of ovarian cancer and showed a symptom of jargon aphasia
Autor:
Takeshi Kihara, Hiroaki Nozaki, Naomi Mezaki, Osamu Onodera, Masatomo Miura, David T.W. Jones, Norikazu Hara, Takanobu Ishiguro, Takuya Konno, Nobuo Ito, Takeshi Ikeuchi, Kenji Okita, Yuichi Tashiro, Yoichi Kanatsuka, Kensaku Kasuga, Miura Takeshi, Dennis W. Dickson, Akio Iwasaki, Zbigniew K. Wszolek, Naoyuki Hara, Yuki Unai, Michitaka Funayama, Takayoshi Tokutake
Publikováno v:
Journal of Neurology
Objective Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is caused by mutations in CSF1R. Pathogenic mutations in exons 12–22 including coding sequence of the tyrosine kinase domain (TKD) of CSF1R were previously id
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 55(5)
We report the case of an 84-year-old man with sensory ataxic polyneuropathy and IgGλ monoclonal gammopathy of undetermined significance (MGUS), which was successfully treated with intravenous immunoglobulin (IVIG) therapy. He had developed progressi