Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Terukuni Imai"'
Autor:
Hidefumi Ito, Yoshiko Tamaru, Junichiro Kawamura, Terukuni Imai, Makito Hirano, Sadayuki Matsumoto, Satoshi Ueno
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 64:469-473
OBJECTIVE Hereditary progressive dystonia with pronounced diurnal fluctuation ((HPD)/dopa responsive dystonia (DRD)) is a childhood onset dystonia which responds to levodopa. Various clinical signs and symptoms of HPD/DRD have been recognised to date
Autor:
Satoshi Kaneko, Hidefumi Ito, Hirofumi Kusaka, Terukuni Imai, Tomoya Nishimura, Hiroo Yoshikawa, Banu Anlar, Reha Kuruo??lu, Kubilay Varli, Meral Top�u, P. Araya, C. Silva, P. Piraino, L. Pedraza, M. E. Wegman, M. Fruns, Juan Idiaquez, Aubrey Ku, Elisabeth Lachmann, Richard Tunkel, Willibald Nagler, Luca Padua, Mauro Lomonaco, Bruno Gregori, Enza Maria Valente, Pietro Tonali, Cumhur Ertekin, Nilg�n Ara�, Burhanettin Uluda??, Zehra Karaca
Publikováno v:
Muscle & Nerve. 19:675-681
Publikováno v:
Acta Neuropathologica. 89:513-518
This report concerns the topographic immunohistochemical analysis of the putamen, globus pallidus (GP) and substantia nigra (SN) of two patients with adult-onset motor neuron disease with basophilic inclusions (MND/BIs), seven patients with sporadic
Autor:
Terukuni Imai, Shiro Yorifuji, Mitsuo Takahashi, Yusaku Nakamura, Nobuya Ogawa, Hisao Tachibana, Ryoichi Yuasa
Publikováno v:
Internal Medicine. 33:517-524
To confirm the clinical utility of selegiline (L-deprenyl), a selective inhibitor of monoamine oxidase B, as an anti-Parkinson's disease (PD) agent, the first Japanese multi-center, double-blind comparative study of this drug was conducted. The subje
Autor:
Haruo Okazaki, Asao Hirano, Terukuni Imai, Satoshi Goto, Nobuyuki Murakami, Yoshio Hashizume, Sadayuki Matsumoto, Hirofumi Kusaka
Publikováno v:
Journal of the Neurological Sciences. 115:208-213
This report concerns the expression of ubiquitin in anterior horn cells of various subgroups of adult and infantile motor neuron disease (MNDs); immunohistochemical techniques were employed. Ubiquitin-positive skein-like inclusions (SLIs) were found
Autor:
Hirofumi Kusaka, Terukuni Imai
Publikováno v:
Journal of Neurology. 239:307-310
A 28-year-old man developed slowly progressive dysarthria and gait disturbance over 7 years. Neurological examination revealed marked ataxia of articulation and gait, mild ataxia and spasticity of all four limbs without intellectual, visual, auditory
Autor:
Chihiro Ihara, Sadayuki Matsumoto, Masataka Nanno, Naoko Maekawa, Sahoko Tamaya, Terukuni Imai, Kazuo Tsuji
Publikováno v:
Nihon Naika Gakkai Zasshi. 89:983-985
症例は63歳,男性.平成9年12月より徐々に食欲不振,筋力低下が出現し甲状腺機能低下を指摘され補充療法を受けたが改善せず,上肢帯筋萎縮及び筋力低下を著明に認め来院.入院後精神症状,
Autor:
Yasushi Hara, Juji Takeuchi, Yoshihiro Takebe, Takanari Yasuda, Tadashi Sakakura, Terukuni Imai
Publikováno v:
Neurosurgery. 26:499-503
Autologous adrenal medulla was transplanted into the putamen of a patient with severe Parkinson's disease. After the operation, the patient's akinesia and rigidity decreased and the duration of action of L-dopa treatment was prolonged. The effect las
Publikováno v:
Annals of Neurology. 40:796-798
We present a new Japanese family with hereditary progressive dystonia with marked diurnal fluctuation/dopa-responsive dystonia. The affected daughter and her asymptomatic father are heterozygous for a novel missense mutation that replaces His by Pro
Publikováno v:
Neurology. 49(2)
This report concerns the characterization of the alpha-tocopherol transfer protein (alpha-TTP) gene in a Japanese family affected by ataxia with isolated vitamin E deficiency (AVED). The sequence analysis revealed a G-to-A transition at the 3' end of