Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tomoko Soeda"'
Autor:
Masahiko Fukatsu, Takenobu Murakami, Hiroshi Ohkawara, Shunichi Saito, Kazuhiko Ikeda, Suguru Kadowaki, Itaru Sasaki, Mari Segawa, Tomoko Soeda, Akihiko Hoshi, Hiroshi Takahashi, Akiko Shichishima-Nakamura, Kazuei Ogawa, Yoshihiro Sugiura, Hitoshi Ohto, Yasuchika Takeishi, Takayuki Ikezoe, Yoshikazu Ugawa
Publikováno v:
BMC Neurology, Vol 17, Iss 1, Pp 1-5 (2017)
Abstract Background Chronic graft-versus-host disease (GVHD) appears several months following allogenic hematopoietic stem cell transplantation (HSCT) and is clinically analogous to autoimmune disorder. Polymyositis is a common neuromuscular disorder
Externí odkaz:
https://doaj.org/article/7529de5c32a149b895ff7e736077ae22
Autor:
Akiko Shichishima-Nakamura, Shunichi Saito, Akihiko Hoshi, Hiroshi Ohkawara, Yasuchika Takeishi, Yoshihiro Sugiura, Kazuei Ogawa, Itaru Sasaki, Suguru Kadowaki, Takenobu Murakami, Mari Segawa, Hiroshi Takahashi, Masahiko Fukatsu, Tomoko Soeda, Takayuki Ikezoe, Hitoshi Ohto, Kazuhiko Ikeda, Yoshikazu Ugawa
Publikováno v:
BMC Neurology, Vol 17, Iss 1, Pp 1-5 (2017)
BMC Neurology
BMC Neurology
Background Chronic graft-versus-host disease (GVHD) appears several months following allogenic hematopoietic stem cell transplantation (HSCT) and is clinically analogous to autoimmune disorder. Polymyositis is a common neuromuscular disorder in chron
Autor:
Yoshikazu Ugawa, Masayo Machii, Shunsuke Kobayashi, Nozomu Matsuda, Tomoko Soeda, Hideyuki Matsumoto
Publikováno v:
Internal Medicine. 54:1415-1419
Post-radiation lower motor neuron syndrome (PRLMNS) is a rare neurological complication of radiation therapy and its pathogenesis is unclear. We herein report a patient with PRLMNS who developed leg weakness 17 years after craniospinal radiation as a
Autor:
Ken Shibano, Kazuhiro Endo, Yoshihiro Sugiura, Yutaka Matsuura, Akihiko Hoshi, Takahiko Yamanoi, Tomoko Soeda, Teiji Yamamoto
Publikováno v:
The Tohoku Journal of Experimental Medicine. 203:133-139
We report three cases of intracranial aspergillosis originating in the sphenoid sinus in immunocompetent patients. The patients presented with an orbital apex syndrome in that a unilateral loss of vision and cranial nerve III palsy were seen in all c
Autor:
Jin Kubo, Tomoko Soeda, Yoshinori Abe, Tomohiro Kumagai, Teiji Yamamoto, Yoshihiro Tanno, Tetsuya Ishihara, Soichi Katayama
Publikováno v:
Internal medicine (Tokyo, Japan). 48(13)
Background Unilateral movement disorders and contralateral neuroimaging abnormalities of the striatum have been sporadically reported as a rare syndrome associated with diabetes mellitus. Despite characteristic imaging findings and clinical manifesta
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 44(8)
A 65-year-old woman with diabetes mellitus and chronic otitis media developed headache, fever, and hoarseness, all of which did not responded to the oral antibiotics. As stiff neck and lower cranial nerve palsies appeared, bacterial meningitis was su
Publikováno v:
BMC Neurology; 2012, Vol. 12 Issue 1, p22-27, 6p, 3 Color Photographs, 1 Black and White Photograph
Publikováno v:
BMC Neurology
BMC Neurology, Vol 12, Iss 1, p 22 (2012)
BMC Neurology, Vol 12, Iss 1, p 22 (2012)
Background Distal myopathy with rimmed vacuoles/hereditary inclusion body myopathy is clinically characterized by the early involvement of distal leg muscles. The striking pathological features of the myopathy are muscle fibers with rimmed vacuoles.