Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Tetsushi Atsumi"'
Autor:
Yasuko Komagata, Tetsushi Atsumi, Hajime Iijima, Toshihiko Ohashi, Masato Tateishi, Kyoichi Ohashi, Yukihiko Hara, Hiroshi Watanabe, Kanki Komiyama, Hiroshi Yamada, Takako Shimizu, Kazuhiro Harada
Publikováno v:
Journal of the American Medical Directors Association. 7:79-83
Objectives To evaluate the effects of tea catechin inhalation on methicillin-resistant Staphylococcus aureus (MRSA) in disabled elderly patients. Design Seven days, randomized, prospective study. Setting Three hospitals in Japan. Participants Seventy
Autor:
A. Robert Spitzer, Shalom Stahl, David Yarnitsky, Ernest W. Johnson, John R. Wilson, R. A. C. Hughes, Stefania Morino, Giovanni Antonini, Kiyotoshi Kaneko, Yoji Ohnishi, Tetsushi Atsumi, Isao Hozumi, Tadashi Miyatake, Tetsuo Furukawa, James P. Knochel, Ikuo Mineo, Seiichiro Tarui, Francis O. Walker, Andrew J. Gitter, Walter C. Stolov, Nicholas J. Capozzoli
Publikováno v:
Muscle & Nerve. 19:531-538
Autor:
Tetsushi Atsumi, Y Hara, X.D Li, Hiroshi Yamada, Hiroshi Watanabe, K. Kosuge, Shinichiro Nishio, H Okabe, T Shimizu, Kyoichi Ohashi
Publikováno v:
Journal of Hospital Infection. 53:229-231
We investigated the effects of inhalation of tea catechin on MRSA in the 24 elderly in patients, who were known to carry MRSA in sputum. The patients in the catechin group (N=12) were administered an inhalation of tea catechin extracts (in saline/bro
Autor:
Shu-ichi Ikeda, Kunihiro Yoshida, Tetsushi Atsumi, Hisayuki Matsuo, Masamitsu Nakazato, Hideaki Shimizu, Shigeru Matsukura, Kazutaka Shiomi, Kenji Kangawa
Publikováno v:
FEBS Letters. 306:206-208
A novel variant transthyretin which contains a leucine-for-valine substitution at position 30 was isolated and identified in the serum of a patient with familial amyloidotic polyneuropathy (FAP). The amino acid substitution was proven to result from
Autor:
Sumio Tanase, Masayuki Ando, Tatsufumi Murakami, Shuichiro Maeda, Kuniko Ishikawa, Shuji Mita, Shukuro Araki, Tetsushi Atsumi, Toshihide Kumamoto
Publikováno v:
Biochemical and biophysical research communications. 187(1)
Summary A novel transthyretin (TTR) mutation associated with familial amyloidotic polyneuropathy was detected in a Japanese patient. Singlestrand conformation polymorphism analysis and sequence analysis of polymerase chain reaction (PCR)-amplified ex
Publikováno v:
Brain and Development. 1:61-67
An unique myopathy described by Ullrich in 1930 was reported in a 4-year-old Japanese boy. Major clinical findings included proximal joint contracture, muscle hypotonia, prominent calcaneus, high-arched palate, and normal intelligence. Muscle biopsy
Autor:
Chikaharu Yabe, Michio Miyapa, Kazushi Takeda, Kogoro Kasahara, Hideo Shimizu, Yoshikazu Yasuda, Yasuhiko Morioka, Yoshikazu Sakamoto, Sumio Tenmoku, Takeshi Kuzuya, Saburo Matsumoto, Tetsushi Atsumi
Publikováno v:
The Japanese Journal of Surgery. 9:350-358
A 34-year-old woman had episodes of hypoglycemic attack 8 years after a surgical resection of a retroperitoneal hemangiopericytoma. In spite of normal levels of serum IRI, insulin radioreceptor assay demonstrated high level of plasma ILA (insulin lik
Autor:
Akemi Suzuki, Tadashi Miyatake, Kyoko Nakamura, Tetsushi Atsumi, Nagashima M, Michiko Sekine, Toshio Ariga, Tamio Yamakawa, Igarashi M
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 752:291-300
The ganglioside content of hog skeletal muscle was 27 nmol/g wet weight when calculated as lipid-bound sialic acid. The elution profile on DEAE-Sephadex A-25 column chromatography showed that the monosialoganglioside fraction (61% of total lipid-boun
Publikováno v:
Acta Neuropathologica. 49:95-100
Inclusions, ultrastructurally identical with Hirano bodies which were previously believed to be limited to the central nervous system (CNS), were found both within peripheral myelinated nerve axons and within terminal axons of neuromuscular junctions
Autor:
Tadashi Miyatake, Masatoyo Nishizawa, E. Ohama, Kazuki Shinozawa, Takeo Kuwabara, Tetsushi Atsumi, Keiko Tanaka
Publikováno v:
Journal of the Neurological Sciences. 78:189-201
We describe a 16-year-old Japanese girl with a mitochondrial encephalomyopathy who presented with progressive dementia, limb weakness and atrophy, episodic vomiting, generalized convulsions, myoclonic seizures, and hypertrophic cardiomyopathy. CT sca