Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Reiko Namba"'
Autor:
Reiko, Namba
Publikováno v:
Brain and nerve = Shinkei kenkyu no shinpo. 67(8)
The neurological disease amyotrophic lateral sclerosis (ALS) requires pain palliation during end-of-life stages. From the view point of a home-care doctor who assists patients with their final wishes to die at home, I summarize the issues involving t
Autor:
Keigo Nobukuni, Yuetsu Ihara, Reiko Namba, Keiko Sato, Hiroshi Takata, Toshiyuki Hayabara, Shinji Miyata
Publikováno v:
Journal of the Japan Epilepsy Society. 17:121-127
Autor:
Reiko Namba, Motoko Kawai, Keiko Sato, Yuetsu Ihara, Keigo Nobukuni, Masayoshi Kibata, Akitane Mori, Toshiyuki Hayabara
Publikováno v:
Journal of the Neurological Sciences. 134:51-56
We studied the relationships between the superoxide dismutase (SOD) activity, free radical (FR) levels and clinical data in patients with sporadic amyotrophic lateral sclerosis (SALS). The SOD activities and blood FR levels of 16 patients with SALS (
Publikováno v:
Internal Medicine. 34:972-975
Autonomic functions were studied in 10 respiratory-support patients with motor neuron disease (MND) at its most advanced stage by means of hemodynamic function tests. The mean duration of disease was 83.4 months (SD 28.0, range 50-140 months). AH the
Autor:
Takashi Nakajima, Utako Nagaoka, Toshio Shimizu, Kiyohiko Kondo, Naoki Fujii, Takayoshi Shimohata, Masatoyo Nishizawa, Ban Mihara, Mitsuru Kawai, Hiroaki Ito, Takashi Imai, Yuki Nakayama, Mieko Ogino, Keigo Nobukuni, Chiharu Kugimoto, Akihiro Kawata, Reiko Namba, Hajime Arahata, Tetsuo Komori, Yoshiyuki Kuroiwa
Publikováno v:
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. 13(4)
Malnutrition in the early stage has been reported as an independent predictor of survival in amyotrophic lateral sclerosis (ALS). We analyzed retrospectively the effect of variation of body mass index (BMI) on survival in ALS patients. In total, 77 c
Autor:
Koji Inui, Takeshi Nakano, Yoshiyuki Suzuki, Akihiro Oshima, Kunihiro Yoshida, Nobuo Yanagisawa, Hitoshi Sakuraba, Shintaro Okada, Reiko Namba, Kiyohiko Kondo, Eiichiro Uyama, Shin-ichi Iwasaki, Kiyoshi Takamiya
Publikováno v:
Annals of Neurology. 31:328-332
Clinical findings were compared with the results of molecular analysis in 16 Japanese patients from 10 unrelated families with the adult/chronic form of GM1 gangliosidosis. Age of onset ranged from 3 to 30 years. Major clinical manifestations were ga
Autor:
Hajime Kodama, Masayoshi Kibata, Akitane Mori, Ken Kamisaka, Yuetsu Ihara, Hajime Fujita, Reiko Namba, Hiroshi Mabuchi, Kouji Kajinami, Keigo Nobukuni, Teruo Shirabe, Koh-ichi Ohshima
Publikováno v:
Journal of the Neurological Sciences. 106:10-18
A study is presented of a 48-year-old female patient and her three siblings with familial hypercholesterolemia. The family members had episodes of cerebral infarction and apparently had atherosclerosis of the internal carotid artery, but no coronary
Autor:
Reiko, Namba
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 33
Palliative care at the end of life for intractable neurological diseases has come into discussion recently. According to the care guidelines for amyotrophic lateral sclerosis (ALS), suggested by the Japan Neurology Societies, neurological doctors sho
Autor:
Reiko, Namba
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 45(11)
Taking into account how to care patients at home with intractable neurological disease and their family, I have introduced the achievement of the medical caring technique by an aged family member, the risks of the PEG and acute respiratory failures u
Autor:
Kenji Uéda, Seishi Terada, Osamu Yokota, Hanae Nakashima, Takeshi Ishihara, Frédéric Checler, Masuyuki Namba, Reiko Namba, Tetsuya Nishinaka, Yasuaki Hayashi, Hiroshi Ujike, Hideki Ishizu, Shigetoshi Kuroda
Publikováno v:
Acta neuropathologica. 106(4)
We describe three cases of early- (cases 1-3, 28-39 years) and one of late-onset (case 4, 76 years) Alzheimer's disease (AD) with 'cotton wool' plaques (CWPs) but without a family history indicating autosomal dominant inheritance. The early-onset cas