Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mika Teraishi"'
Autor:
Mayuko Yamamoto, Shigetoshi Sano, Haruka Kobashi, Hozumi Sano, Ema Kusume, Mika Teraishi, Tokuko Oguro, Ai Fujioka, Hideki Nakajima
Publikováno v:
The Journal of Dermatology
Pralatrexate has been approved for the treatment of relapsed/refractory peripheral T cell lymphomas. Studies in the U.S. also support the clinical efficacy of pralatrexate to treat advanced‐stage cutaneous T‐cell lymphomas, but outcomes in Japane
Autor:
Hideki Nakajima, Yukiko Aoyama, Shigetoshi Sano, Mayuko Yamamoto, Mika Teraishi, Kimiko Nakajima
Publikováno v:
The Journal of dermatologyREFERENCES. 48(11)
Publikováno v:
Nishi Nihon Hifuka. 81:311-315
Autor:
Nagamasa Maeda, Mika Teraishi, Shigetoshi Sano, Tatsushi Ishimoto, Mayuko Yamamoto, Kimiko Nakajima, Yoshinao Muro
Publikováno v:
International Journal of Rheumatic Diseases. 21:900-902
Autor:
Shigetoshi Sano, Mika Teraishi, Mitsunori Ikeda, Takahisa Furukawa, Atsushi Hijikata, Yoko Hiraki, Seiji Mizuno, Yujiro Higashi, Yoshinobu Asada, Mikiro Takaishi, Nobuaki Wakamatsu, Kimiko Nakajima, Shinji Shimoda, Toshiyuki Fukada, Osamu Ohara
Publikováno v:
Scientific Reports
Mowat-Wilson syndrome (MOWS) is a congenital disease caused by de novo heterozygous loss of function mutations or deletions of the ZEB2 gene. MOWS patients show multiple anomalies including intellectual disability, a distinctive facial appearance, mi
Publikováno v:
Nishi Nihon Hifuka. 74:22-26
45歳,女性。初診の3ヵ月前より両下腿に紅斑,紫斑,潰瘍が出現した。初診時,両下腿および内足縁に網状の紅斑,紫斑が散在し,一部に痂皮を付着する潰瘍を認めた。病理組織では真
Autor:
Kazumi Matsuda, Hideki Nakajima, Mayuko Yamamoto, Hideki Kishimoto, Shigetoshi Sano, Masahito Tarutani, Maki Yokogawa, Chie Kitagawa, Mika Teraishi
Publikováno v:
Skin Cancer. 26:69-72
Publikováno v:
Journal of Dermatological Science. 84:e22-e23
Autor:
Mika Teraishi, Kimiko Nakajima, Shigetoshi Sano, Yoshikazu Uchida, Hiroshi Shimizu, Mayuko Yamamoto, Mayumi Ujihara, Masashi Akiyama
Publikováno v:
Journal of Dermatological Science. 57:102-107
Background Dorfman–Chanarin syndrome (DCS), also referred to as neutral lipid storage disease with ichthyosis, is a rare autosomal recessive form of nonbullous congenital ichthyosiform erythroderma, characterized by the presence of intracellular li
Autor:
Kimiko Nakajima, Toshiyuki Fukada, Yoshinobu Asada, Mika Teraishi, Takahisa Furukawa, Mikiro Takaishi, Shinji Shimoda, Yoko Hiraki, Shigetoshi Sano, Seiji Mizuno, Nobuaki Wakamatsu
Publikováno v:
Journal of Dermatological Science. 84:e139