Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Seijiro, Aso"'
Autor:
Kumiko Yanagi, Jonathan Coker, Kaori Miyana, Seijiro Aso, Nana Kobayashi, Kazuhito Satou, Adam Richman, Suneel Indupuru, Yoichi Matsubara, Tadashi Kaname
Publikováno v:
Journal of Human Genetics.
Autor:
Nobuhiko Okamoto, Tadashi Matsumoto, Yuri Dowa, Yasutsugu Chinen, Masafumi Fukuda, Kenji Shimizu, Katsuya Tashiro, Seiji Mizuno, Kyoko Minagawa, Yoko Hiraki, Yoshihiro Toda, Osamu Shimokawa, Toshiyuki Yamamoto, Hirofumi Ohashi, Satoshi Watanabe, Seijiro Aso, Koichi Shichijo, Natsuko Shiomi, Kazunori Minatozaki, Tatsuro Kondoh, Hiroyuki Moriuchi, Keiko Shimojima, Rika Kosaki, Koh-ichiro Yoshiura
Publikováno v:
American Journal of Medical Genetics Part A. 170:908-917
Partial 1q trisomy syndrome is a rare disorder. Because unbalanced chromosomal translocations often occur with 1q trisomy, it is difficult to determine whether patient symptoms are related to 1q trisomy or other chromosomal abnormalities. The present
Publikováno v:
Nihon rinsho. Japanese journal of clinical medicine. 66(2)
We defined incomplete Kawasaki disease (KD) as those having less than 5 principal symptoms of KD in this article. Japanese Nationwide KD surveys revealed that the prevalence of coronary artery lesion in incomplete KD is almost the same as that of com
Autor:
Seijiro Aso, Yoshikazu Nakamura, Tomoyoshi Sonobe, Nobuyuki Kiyosawa, Hiroshi Yanagawa, Yoshio Imada, Mayumi Yashiro, Yoko Imai, Keiji Tsuchiya
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 49(4)
Background: The aim of the present study was to determine the prevalence of coronary artery abnormality (CAA) and other clinical features in patients with incomplete Kawasaki disease (iKD) using the data from the 17th Japanese nationwide survey of KD
Autor:
Kayoko Saito, Keiko Shimojima, Shino Shimada, Noriko Sangu, Seijiro Aso, Mari Matsuo, Toshiyuki Yamamoto
Publikováno v:
Molecular Cytogenetics
Background Triplication is a rare chromosomal anomaly. We identified a de novo triplication of 11q12.3 in a patient with developmental delay, distinctive facial features, and others. In the present study, we discuss the mechanism of triplications tha
Autor:
Hiroshi Yanagawa, Yoshio Imada, Yosikazu Nakamura, Tomoyoshi Sonobe, Seijiro Aso, Keiji Tsuchiya
Publikováno v:
Pediatric Research. 53:164-164
Purpose: To clarify the incidence of coronary artery abnormality (CAA) among incomplete (atypical) Kawasaki disease.Method: We defined incomplete cases as follows. The incomplete Kawasaki disease of narrow definition (nd-IKD) consists of cases with 4
Autor:
Masaki Nagai, Itsuzo Shigematsu, Seijiro Aso, Hiroshi Yanagawa, Yoshio Imada, Mayumi Yashiro, Yosikazu Nakamura, Tomisaku Kawasaki, Yasuyuki Fujita
Publikováno v:
Journal of Infectious Diseases. 158:1296-1301
Nationwide epidemiological surveys of Kawasaki disease have been conducted nine times in Japan since 1970. By the end of 1986, 83,857 (male:female ratio, 1.4) cases were reported. We summarize the results of these surveys, especially the latest surve
Publikováno v:
Pediatrics International. 24:408-409