Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Chun Feng Tan"'
Autor:
Nishihira, Yasushi1 pathjim@bri.niigata-u.ac.jp, Chun-Feng Tan1, Toyoshima, Yasuko1, Yonemochi, Yosuke2, Kondo, Hiroshi3, Nakajima, Takashi2, Takahashi, Hitoshi1
Publikováno v:
Neuropathology. Dec2009, Vol. 29 Issue 6, p689-696. 8p. 3 Color Photographs, 1 Black and White Photograph, 1 Chart.
Autor:
Nishihira, Yasushi1 yashiyashi100@bri.niigata-u.ac.jp, Chun-Feng Tan1, Hirato, Junko2, Yoshimura, Junichi3, Nishiyama, Kenichi3, Takahashi, Hideaki3, Fujii, Yukihiko3, Takahashi, Hitoshi1
Publikováno v:
Neuropathology. Dec2007, Vol. 27 Issue 6, p551-555. 5p. 1 Black and White Photograph, 2 Diagrams.
Autor:
Hitoshi Takahashi, Taisuke Kato, Yukari Miki, Chun Feng Tan, Masatoyo Nishizawa, Yuko Ariizumi, Akihide Koyama, Atsushi Shiga, Akiyoshi Kakita, Tatsuya Sato, Akio Yokoseki, Takeshi Fujino, Osamu Onodera, Tomohiko Ishihara, Mariko Yokoo
Publikováno v:
Human Molecular Genetics. 22:4136-4147
Disappearance of TAR-DNA-binding protein 43 kDa (TDP-43) from the nucleus contributes to the pathogenesis of amyotrophic lateral sclerosis (ALS), but the nuclear function of TDP-43 is not yet fully understood. TDP-43 associates with nuclear bodies in
Autor:
Takayuki Kosaka, Yong-Juan Fu, Haruka Ishidaira, Chun-Feng Tan, Atsushi Shiga, Osamu Onodera, Ryoko Koike, Takashi Tani, Hitoshi Takahashi, Masatoyo Nishizawa, Akiyoshi Kakita
Publikováno v:
Neuropathology. 32:373-384
Primary lateral sclerosis (PLS) is clinically defined as a disorder selectively affecting the upper motor neuron (UMN) system. However, recently it has also been considered that PLS is heterogeneous in its clinical presentation. To elucidate the asso
Autor:
Yasuko Toyoshima, Yasushi Nishihira, Hitoshi Takahashi, Yosuke Yonemochi, Chun-Feng Tan, Takashi Nakajima, Hiroshi Kondo
Publikováno v:
Neuropathology. 29:689-696
It has been reported that widespread multisystem degeneration can occur in patients with sporadic amyotrophic lateral sclerosis (SALS) who have survived for long periods with artificial respiratory support (ARS). We report a case of SALS of 8 years a
Autor:
Izumi Kawachi, Takashi Morita, Hitoshi Takahashi, Chun-Feng Tan, Keisuke Iwanaga, Yasuhiro Hoshi, Megumi Yamada, Isao Hozumi, Osamu Onodera, Yasushi Nishihira, Masatoyo Nishizawa, Akiyoshi Kakita, Mitsuhiro Tsujihata
Publikováno v:
Acta Neuropathologica. 117:45-53
Recently, sporadic amyotrophic lateral sclerosis (SALS), a fatal neurological disease, has been shown to be a multisystem proteinopathy of TDP-43 in which both neurons and glial cells in the central nervous system are widely affected. In general, the
Autor:
Yasuko Toyoshima, Osamu Onodera, Hitoshi Takahashi, Chun-Feng Tan, Yasushi Nishihira, Takashi Morita, Akiyoshi Kakita, Masatoyo Nishizawa, Mitsunori Yamada
Publikováno v:
Acta Neuropathologica. 116:169-182
A nuclear protein, 43-kDa TAR DNA-binding protein (TDP-43), was recently identified as a component of the ubiquitinated inclusions (UIs) in frontotemporal lobar degeneration (FTLD-U) and sporadic amyotrophic lateral sclerosis (SALS). In the present s
Autor:
Junko Hirato, Yasushi Nishihira, Kenichi Nishiyama, Hitoshi Takahashi, Hideaki E. Takahashi, Junichi Yoshimura, Yukihiko Fujii, Chun-Feng Tan
Publikováno v:
Neuropathology. 27:551-555
Two embryonal CNS tumors, atypical teratoid/rabdoid tumor (AT/RT) and primitive neuroectodermal tumor (PNET), may be confused with each other and misdiagnosed. Here we report an infant with a congenital supratentorial tumor, which was detected by fet
Autor:
Masanao Saio, Takashi Inuzuka, Chun-Feng Tan, Hitoshi Takahashi, Isao Hozumi, Kenji Wakida, Akio Kimura
Publikováno v:
Neuropathology. 27:284-289
We report a rapidly progressive myelopathy in a 74-year-old Japanese man who was admitted to our hospital with a 4-month history of progressive gait disturbance and died of pneumonia followed by respiratory failure on the 22nd day of admission. Durin
Autor:
Keisuke Iwanaga, Akiyoshi Kakita, Tammaryn Lashley, Chun-Feng Tan, Yue-Shan Piao, Hiroki Takano, Masatoyo Nishizawa, Rohan de Silva, Mitsuhiro Tsujihata, Hitoshi Takahashi, Tamas Revesz, Andrew J. Lees
Publikováno v:
Acta Neuropathologica. 110:600-609
We report a sporadic tauopathy of 6-year duration in a 76-year-old woman. Her initial symptoms were asymmetrical parkinsonism and muscle weakness, with apraxia appearing 2 years later. The brain showed frontal and temporal cerebral atrophy; severe ne