Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Satoru Ohba"'
Publikováno v:
Practica Oto-Rhino-Laryngologica. 106:687-691
Publikováno v:
Practica Oto-Rhino-Laryngologica. 106:235-240
Autor:
Daisuke Ichikawa, Yukiko Kubota, Satoru Ohba, Takashi Nakagawa, Toshifumi Sakata, Tetsuko Ueno
Publikováno v:
AUDIOLOGY JAPAN. 56:218-225
Autor:
Hideki Miyaguchi, Tadashi Akiyama, Tamiko Shinohara, Satoru Ohba, Tatsuro Ikeuchi, Toshiaki Shimizu, Takashi Shibata
Publikováno v:
Clinical Genetics. 33:311-314
A female infant with distal trisomy 17q is described. The anomaly resulted from a de novo inverted duplication of the 17q2405----q25.3 region as defined by high-resolution banding. The proband's overall clinical picture was in good agreement with tho
Autor:
Akihito Ueta, Yumiko Ohkubo, Satoshi Sumi, Hajime Togari, Tetsuya Ito, Satoru Ohba, Ineko Kato
Publikováno v:
Gout and Nucleic Acid Metabolism. 29:127-131
Autor:
H. Fujimoto, Michael P. Federle, Tsutomu Araki, A. Sugiyama, Hiroki Haradome, Satoru Ohba, Tomoaki Ichikawa, Kuni Ohtomo
Publikováno v:
Abdominal Imaging. 25:409-419
Background: Our purpose was to review a series of 14 patients with atypical exocrine and endocrine pancreatic tumors to derive characteristic computed tomographic and pathologic features that might allow better diagnosis, categorization, and manageme
Autor:
Satoshi Sumi, Masayuki Imaeda, Kiyoshi Kidouchi, Kyoko Kodama, Hajime Togari, Satoru Ohba, Yoshiro Wada, Shinji Fujimoto
Publikováno v:
The Tohoku Journal of Experimental Medicine. 190:23-32
A screening system for pyrimidine metabolism disorders by measurement with high-performance liquid chromatography using dried filter-paper urine samples is presented. This system permits the simultaneous determination of dihydrouracil, uracil, orotic
Autor:
M Kouwaki, Masaru Nonaka, Yoshiro Wada, Jan J. Rotteveel, Makoto Sasaki, R.A. de Abreu, M Imaeda, Satoshi Sumi, A. B. P. Van Kuilenburg, Peter Vreken, Y Endo, Koichi Matsuda, Satoru Ohba, Naoki Hamajima, Kiyoshi Kidouchi, A. H. van Gennip, H Togari, Nanaya Tamaki
Publikováno v:
American Journal of Human Genetics, 63, 717-726
American journal of human genetics, 63(3), 717-726. Cell Press
American Journal of Human Genetics, 63, pp. 717-726
American journal of human genetics, 63(3), 717-726. Cell Press
American Journal of Human Genetics, 63, pp. 717-726
SummaryDihydropyrimidinase (DHP) deficiency (MIM 222748) is characterized by dihydropyrimidinuria and is associated with a variable clinical phenotype. This disease might be associated with a risk of 5-fluorouracil toxicity, although no cases have be
Autor:
Shigeru Sasaki, T. Terazawa, Yasushi Matsushita, M. Mizutani, K. Ando, Hirokazu Mizutani, Satoru Ohba, T. Ohtsuka, S. Ijima
Publikováno v:
Acta Radiologica. 39:269-272
We report on specific CT and MR features in two cases of tumoral calcium pyrophosphate dihydrate deposition disease in the shoulder with unusually large tumors. CT revealed features that were specific to the disease. MR was useful for detecting the e
Autor:
Mitsuo Yatsuzuka, Satoru Ohba, Kuni Ohtomo, Tomoaki Ichikawa, Hajime Fujimoto, Mitsuo Honma, Yoichiro. Nakajima, Akihiro Koyama, Guio Uchiyama, Shinichiro Ushigome
Publikováno v:
Skeletal Radiology. 26:602-605
We present a case of giant calcifying epithelioma of Malherbe (pilomatrixoma) in the right upper arm of a 62-year-old man. It measured 18 x 12 x 8 cm in size, making it the largest of all the cases reported previously. CT clearly demonstrated a well-