Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kyoichi Ohtani"'
Autor:
Masashi Mizuguchi, Etsuo Okazaki, Mitsuo Takahashi, Kyoichi Ohtani, Yasutsugu Kobayashi, Michihiko Narita, Masayuki Itoh, Yoshiko Nakai, Takehiro Togashi, Akira Ogawa, Hiroshi Ozawa, Sachio Takashima
Publikováno v:
Acta Neuropathologica. 105:233-239
During influenza epidemics in Japan, the number of children with acute encephalopathies and encephalitis has recently increased. Although the pathophysiologies remain unclear, there is usually brain edema with evidence of damage to the blood-brain-ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6daaa91aa906869d7326565b50f6c1f
https://doi.org/10.1007/s00401-002-0605-x
https://doi.org/10.1007/s00401-002-0605-x
Autor:
Kenzo Takeshita, Kyoichi Ohtani
Publikováno v:
Congenital Anomalies. 40:269-274
In detecting changes of the occurrence of birth malformation it is important to indicate the prevalence of environmental hazards. The Tottori Monitoring System for Birth Defects (TOM) is a small regional system covering 6,000 births yearly which was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55695adf38f09d8955136fadfedeb70b
https://doi.org/10.1111/j.1741-4520.2000.tb00924.x
https://doi.org/10.1111/j.1741-4520.2000.tb00924.x
Autor:
Takayuki Kohda, Kana Santou, Mikio Tsunei, Tadataka Hoshika, Kyoichi Ohtani, Isao Nakamura, Takehumi Hurukawa, Hidemasa Iwakura, Hideaki Oti, Katsuyuki Ashihara
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 13:151-156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cedd19a9ebbba2e835c13981ae20ef38
https://doi.org/10.3165/jjpn.13.151
https://doi.org/10.3165/jjpn.13.151
Publikováno v:
Pediatric Neurology. 19:199-203
The authors studied the epidemiology of spina bifida in Tottori Prefecture, Japan, from 1976 to 1995. Thirty-four patients (16 men and 18 women) were registered in this study. Consanguineous marriages, familial occurrence, and abnormalities in prenat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9e16b647fdbded9329651f5c8ad85ff
https://doi.org/10.1016/s0887-8994(98)00048-4
https://doi.org/10.1016/s0887-8994(98)00048-4
Publikováno v:
Brain and Development. 19:436-439
A 2-year-old girl with bilateral sensorineural deafness showed pontine hypoplasia as well as a bulging contour of the pontine tegmentum on magnetic resonance imaging (MRI). There were no bilateral responses of brainstem auditory-evoked potentials (BA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d50212aafe20340480e66b27e8049b2
https://doi.org/10.1016/s0387-7604(97)00056-9
https://doi.org/10.1016/s0387-7604(97)00056-9
Publikováno v:
Pediatrics International. 37:125-128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc19888b814e48d120875c1f0b0d48d6
https://doi.org/10.1111/j.1442-200x.1995.tb03705.x
https://doi.org/10.1111/j.1442-200x.1995.tb03705.x
Autor:
Yasushi Utsunomiya, Hiroshi Hayashibara, Motoaki Morita, Tadataka Hoshika, Mikio Tsunei, Masato Hirao, Teruo Okasora, Makoto Urushibara, Kyoichi Ohtani
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 8:217-220
特発性ネフローゼ症候群 (以下，ネ症) の中には緩徐な経過でネ症に至る症例や病初期にはネ症の診断基準を満たすが，経過観察のみで自然に軽快する非典型的な経過をとる症例がみられ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e977b7748c049df76b71f816ba2b0898
https://doi.org/10.3165/jjpn.8.217
https://doi.org/10.3165/jjpn.8.217
Autor:
Kenzo Takeshita, Isao Yuasa, Shinjirou Akaboshi, Toshiyuki Yamamoto, Kyoichi Ohtani, Tadashi Terada, Shu Nakamoto, Yukisato Kitamura, Haidi Zhang, Eiji Nanba, Kousaku Ohno
Publikováno v:
American Journal of Medical Genetics. 82:368-370
A Japanese patient with tuberous sclerosis (TSC), who manifested with multiple lung cysts and pneumothorax, is described. All exons of two TSC genes, TSC1 and TSC2, in peripheral blood leukocytes from the patient were analyzed by polymerase chain rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a894e09d6ff3250c83de2131ad89438b
https://doi.org/10.1002/(sici)1096-8628(19990219)82:5<368::aid-ajmg2>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19990219)82:5<368::aid-ajmg2>3.0.co
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
Autor:
Toshiyuki, Yamamoto, Yuko, Akasaka, Kyoichi, Ohtani, Takashi, Hayashi, Shiro, Kashiwagi, Takashi, Ichiyama, Miki, Nishikawa, Mitsuhiro, Kato, Yoshihiro, Maegaki, Akira, Oka, Kousaku, Ohno
Publikováno v:
No to hattatsu = Brain and development. 37(1)
Moyamoya disease is a cerebrovascular disorder of unknown etiology. Its high incidence in East Asia and accumulation in family members suggest a genetic background. A high incidence of maternal inheritance implicates genomic imprinting in this disord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c62c90cefdc90a72d5e0a74de8a94780
https://pubmed.ncbi.nlm.nih.gov/15675354
https://pubmed.ncbi.nlm.nih.gov/15675354