Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shizuko Murayama"'
Autor:
Masahiro Tachi, Toshio Nakajo, Takahiko Moriguchi, Takehiko Ohura, Hiroaki Oka, Reiko Nogami, Norihiko Ohura, Shizuko Murayama
Publikováno v:
Wound Repair and Regeneration. 19:542-551
A basic fibroblast growth factor (bFGF) case and a control case whose total scores of Pressure Ulcer Healing Process-Ohura (PUHP-Ohura) and risk factors for pressure ulcers, and level of care for pressure ulcers were equivalent were paired. Twenty-th
Autor:
Yasushi Deguchi, Hirosumi Mori, Shizuko Murayama, Tomoko Fujita, Sayaka Takanashi, Toshitaka Kohagizawa, Kumiko Takahashi, Sachiko Miyatsuka, Shinichi Kobayashi, Masato Nagata, Nobuhiko Okabe, Osamu Tatsuzawa, Yuichi Koike, Yasuyuki Wada, Kaoru Higuchi, Sadato Ichinohe, Tatsuya Sato, Hiroaki Wakasugi
Publikováno v:
European Journal of Pediatrics. 167:1389-1394
In this paper, we examined the details of severe infections, treatment efficacies, and the prognoses of 23 Japanese patients with chronic granulomatous disease (CGD). We described the mean ages at diagnosis and follow-up, which were 2.8 years (range,
Autor:
Hiromi Sanada, Junko Sugama, Brian Thigpen, Suriadi, Shizuko Murayama, Sachiko Kinosita, Atsuko Kitagawa
Publikováno v:
Journal of Tissue Viability. 16:21-26
The purpose of this study was to assess the utility of two instruments (the Braden scale and a multi-pad pressure evaluator) for predicting pressure ulcer development. A prospective cohort design was used and 105 intensive care unit patients particip
Autor:
Yasuyuki Wada, Shizuko Murayama, Hiroyuki Namba, Shinji Kunishima, Masaharu Akiyama, Hiroyuki Ida
Publikováno v:
Pediatrics International. 55:102-104
We report familial cases with MYH9 disorders: a 1-year-old Japanese boy who presented only with macrothrombocytopenia, and his 33-year-old father who had been diagnosed with refractory chronic idiopathic thrombocytopenic purpura, and suffered from he
Autor:
Kentaro Yokoi, Kohji Fujisawa, Yoshikatsu Eto, Takaki Yanagisawa, Masaharu Akiyama, Yukio Hattori, Shizuko Murayama, Yasuhiro Yamashiro
Publikováno v:
Pediatric Blood & Cancer. 47:839-841
Hemoglobin Hammersmith, a rare, unstable hemoglobin variant, was diagnosed in a 9-year-old Japanese girl. She presented with the typical manifestations of this disorder, including neonatal hyperbilirubinemia, followed by progressive hepatosplenomegal
Autor:
Shizuko, Murayama, Masaharu, Akiyama, Hiroyuki, Namba, Yasuyuki, Wada, Hiroyuki, Ida, Shinji, Kunishima
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 55(1)
We report familial cases with MYH9 disorders: a 1-year-old Japanese boy who presented only with macrothrombocytopenia, and his 33-year-old father who had been diagnosed with refractory chronic idiopathic thrombocytopenic purpura, and suffered from he
Autor:
Takehiko, Ohura, Toshio, Nakajo, Takahiko, Moriguchi, Hiroaki, Oka, Masahiro, Tachi, Norihiko, Ohura, Reiko, Nogami, Shizuko, Murayama
Publikováno v:
Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society. 19(5)
A basic fibroblast growth factor (bFGF) case and a control case whose total scores of Pressure Ulcer Healing Process-Ohura (PUHP-Ohura) and risk factors for pressure ulcers, and level of care for pressure ulcers were equivalent were paired. Twenty-th
Autor:
Goro Koinuma, Chikako Kiyotani, Masaaki Kumagai, Shinichi Kobayashi, Osamu Tatsuzawa, Kazuteru Kawasaki, Shizuko Murayama
Publikováno v:
European journal of pediatrics. 166(3)
In this report, we describe a patient with X-linked severe combined immunodeficiency (X-SCID) who had high serum IgG, IgA, and IgM levels. The boy did well until 6 months of age, when he developed interstitial pneumonia caused by Aspergillus species,