Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Tomomi Honma"'
Autor:
Masumi, Murakami, Ryo, Shimizu, Takayuki, Kasai, Tomomi, Honma, Yamato, Niioka, Reiko, Nakashima, Manabu, Onishi, Ken, Takaya, Tokiko, Sakurada, Toyohiko, Osanai
Publikováno v:
青森保健医療福祉研究 = Aomori Journal of Health and Welfare. 4(1):40-47
〔目的〕 ニーズ調査の結果から,学生キャリア開発科の活動に関連する内容を報告する。採用に関する課題や県内定着率が低い理由等の検討によって,今後の活動への示唆を得る。〔方
Publikováno v:
青森保健医療福祉研究 = Aomori Journal of Health and Welfare. 3(1):10-19
〔目的〕本研究は,外来がん薬物療法を受ける患者を支援するための外来チーム医療の実際と課題を明らかにすることを目的とした。〔方法〕がん診療連携拠点病院5 施設の専門職者33名
Publikováno v:
青森保健医療福祉研究 = Aomori Journal of Health and Welfare. 2(2):36-42
[目的] フルスケールシミュレーション教育において,デブリーフィングは特に重要とされているものの,デブリーフィングを実施する教員と学生との関わりや,これらの場面の振り返り
Publikováno v:
青森保健医療福祉研究 = Aomori Journal of Health and Welfare. 2(2):28-35
[目的] 看護学生が実習の場で看護技術を経験できる機会は,患者の高齢化や重症化,看護業務の多様化などの背景から限定されてきている。その結果,看護基礎教育で習得した能力と看
Autor:
Tomomi Honma
Publikováno v:
The Japanese Journal of Educational Psychology. 51:390-400
Autor:
Takashi Shiihara, Masanori Adachi, Gen Nishimura, Shiro Ikegawa, Makoto Mikawa, Eiji Nakajima, Noriyo Manabe, Tomomi Honma, Yoshimitsu Fukushima
Publikováno v:
American Journal of Medical Genetics Part A. :147-153
We describe a 5-year-old boy and a 33-year-old woman with spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form (spondyloepimetaphyseal dysplasia with multiple dislocations) (MIM 6003546), and two 12-year-old girls with the disorder w
Autor:
Tomomi Honma
Publikováno v:
The Japanese Journal of Educational Psychology. 48:32-41
Autor:
Kazuyuki Nakamura, Yumiko Kishikawa, Chikahiko Numakura, Akiko Abe, Tomomi Honma, Emi Shirahata, Mitsuhiro Kato, Chizuru Seiwa, Kiyoshi Hayasaka, Aiko Itoh
Publikováno v:
Journal of human genetics. 55(11)
We present a 3⅓-year-old girl with severe Charcot-Marie-Tooth disease type 1 (Dejerine-Sottas disease), who was a compound heterozygote carrying a deletion of the whole peripheral myelin protein 22 (PMP22) and a deletion of exon 5 in the other PMP2
Autor:
Aiko Ito, Mitsuhiro Kato, Kiyoshi Hayasaka, Takashi Shiihara, Shinjiro Akaboshi, Tomomi Honma, Eiji Nanba, Kenji Tsuburaya
Publikováno v:
Annals of Neurology. 47:514-516
We investigated the molecular basis of holoprosencephaly in a sporadic patient and identified a novel missense mutation in the signal sequence of the sonic hedgehog (Shh) gene. Magnetic resonance imaging of the head showed a lobar type of holoprosenc
Autor:
Tomomi Honma, Takashi Shiihara, Mitsuhiro Kato, Kiyoshi Hayasaka, Hiroko Kodama, Akira Matsunaga, Toshiyuki Kimura
Publikováno v:
Journal of child neurology. 17(5)
We report a 19-month-old boy with Menkes' syndrome that was complicated by a progressive sliding hiatal hernia. He presented with convulsions, developmental delay, elongation and tortuosity of major cerebral arteries, and diverticulae of the bladder