Zobrazeno 1 - 10
of 15
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bf433626a0f20216b5bb0f12689eeb0
https://doi.org/10.1038/s10038-023-01130-8
https://doi.org/10.1038/s10038-023-01130-8
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c98ccd41c82227ca49079a5e29ad036f
https://doi.org/10.1002/ajmg.a.37496
https://doi.org/10.1002/ajmg.a.37496
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4169d134ca3dd69f37d4df52acbd087c
https://pubmed.ncbi.nlm.nih.gov/18260331
https://pubmed.ncbi.nlm.nih.gov/18260331
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1d7d477311a036b5948f5203388c0a6
https://pubmed.ncbi.nlm.nih.gov/17587261
https://pubmed.ncbi.nlm.nih.gov/17587261
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6eca4dfd51b32b85abfc2c8476457cf
https://doi.org/10.1186/1755-8166-6-15
https://doi.org/10.1186/1755-8166-6-15
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dddb44841efb29449bb1f74b9c85ced
https://doi.org/10.1203/00006450-200301000-00061
https://doi.org/10.1203/00006450-200301000-00061
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b102e73057e30d225665f3a40fca6991
https://doi.org/10.1093/infdis/158.6.1296
https://doi.org/10.1093/infdis/158.6.1296
Publikováno v:
Pediatrics International. 24:408-409
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfb63f4042691fc3af8baef633dda9fd
https://doi.org/10.1111/j.1442-200x.1980.tb00558.x
https://doi.org/10.1111/j.1442-200x.1980.tb00558.x
Autor:
Watanabe, Satoshi, Shimizu, Kenji, Ohashi, Hirofumi, Kosaki, Rika, Okamoto, Nobuhiko, Shimojima, Keiko, Yamamoto, Toshiyuki, Chinen, Yasutsugu, Mizuno, Seiji, Dowa, Yuri, Shiomi, Natsuko, Toda, Yoshihiro, Tashiro, Katsuya, Shichijo, Koichi, Minatozaki, Kazunori, Aso, Seijiro, Minagawa, Kyoko, Hiraki, Yoko, Shimokawa, Osamu, Matsumoto, Tadashi
Publikováno v:
American Journal of Medical Genetics. Part A; Apr2016, Vol. 170A Issue 4, p908-917, 10p
Autor:
SONOBE, TOMOYOSHI, KIYOSAWA, NOBUYUKI, TSUCHIYA, KEIJI, ASO, SEIJIRO, IMADA, YOSHIO, IMAI, YOKO, YASHIRO, MAYUMI, NAKAMURA, YOSHIKAZU, YANAGAWA, HIROSHI
Publikováno v:
Pediatrics International; Aug2007, Vol. 49 Issue 4, p421-426, 6p, 6 Charts