Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ariko Takeuchi"'
Autor:
Tatsuya Koeda, Hiraku Ishida, Reiko Ishigami, Ariko Takeuchi, Shinako Terakawa, Katsutoshi Kobayashi, Ayumi Seki, Toshitaka Tamaru, JCS group
Publikováno v:
Journal of Epidemiology
Background: The Tottori study group, part of the JCS, presides over a community-based cohort study started when subjects—children living in Tottori City—were 5 years old. The social aspects of conducting a cohort study should also be made public,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bd62cd84d64639bf8ccb671e1a66f77
https://doi.org/10.2188/jea.je20090191
https://doi.org/10.2188/jea.je20090191
Autor:
Kichizo Yamamoto, Atsushi Ieshima, Masaki Ikeda, Hiroshi Hagino, Ariko Takeuchi, Mitsuyoshi Takata
Publikováno v:
Orthopedics & Traumatology. 39:1349-1352
The Lowe syndrome is characterized by rickets, bone changes, hypotonia, absence of deep tendon reflex, cataract, glaucome, metabolic acidosis, aminoaciduria and such.An 8-year-old boy of this syndrome was reported. Thinning of cortex was observed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2844602fb8e2b6fc14b681c9d233907
https://doi.org/10.5035/nishiseisai.39.1349
https://doi.org/10.5035/nishiseisai.39.1349
Autor:
Kousaku Ohno, Kenzo Takeshita, Ikuo Nagata, Yoshihiro Maegaki, Kyoichi Ohtani, Ariko Takeuchi, Hiroaki Ehara, Yukiko Nanba, Mitsuo Toyoshima, Akiko Kondo, Shoji Nakai
Publikováno v:
American journal of medical genetics. Part A. (11)
One hundred sixty-four patients with Down syndrome (DS) were confirmed in Tottori Prefecture, Japan, from 1980 to 1999. The sex ratio of 1.52 (99 males and 65 females) was comparable to that reported in previous studies. The live birth prevalence per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe9a53c7f0abbaa77892fff168e0fa45
https://pubmed.ncbi.nlm.nih.gov/18412274
https://pubmed.ncbi.nlm.nih.gov/18412274
Publikováno v:
American journal of medical genetics. 49(3)
We report on a 16-year-old girl with spondyloepiphyseal dysplasia, nephrotic syndrome, lymphopenia, and signs of defective cellular immunity. The manifestations are very similar to those reported by Spranger et al. [1991: J. Pediatr 119: 64-72] as Sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27f0ba32b5e12c81c42c75c2271114ad
https://pubmed.ncbi.nlm.nih.gov/8209883
https://pubmed.ncbi.nlm.nih.gov/8209883