Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Mariko, Tsujimoto"'
Autor:
Sae Murakami, Shinichi Moriwaki, Yasumasa Kakei, Chikako Nishigori, Mariko Tsujimoto, Nozomi Yamano, Takeshi Fujita, Takehiro Ueda, Ryusuke Ono
Publikováno v:
BMJ Open, Vol 13, Iss 3 (2023)
Introduction Xeroderma pigmentosum (XP) is a rare intractable disease without a fundamental treatment, presenting with severe photosensitivity, freckle-like pigmented and depigmented maculae and numerous skin cancers before the age of 10 years withou
Externí odkaz:
https://doaj.org/article/d11cba17fda1448db1a236ec2b8d72be
Autor:
Seiji, Takeuchi, Toshiro, Matsuda, Mariko, Tsujimoto, Takeshi, Fukumoto, Ryusuke, Ono, Chikako, Nishigori
Publikováno v:
Journal of Dermatological Science. 105:152-158
Xeroderma pigmentosum (XP) is hereditary disorder characterized by photosensitivity, predisposition to skin cancers of sun-exposed body sites and progressive neurologic symptoms in some cases. Cells from XP patients show higher sensitivity to ultravi
Autor:
Mariko Tsujimoto, Eiji Nakano, Yuka Nakazawa, Fumio Kanda, Takehiro Ueda, Tomoo Ogi, Chikako Nishigori
Publikováno v:
The Journal of dermatologyREFERENCES.
We present a mild case of Cockayne syndrome that was referred to us with an extreme sunburn at the age of 3. In early teens, although her cutaneous symptoms alleviated without any medications, she developed tremor and dysarthria. Neurological examina
Autor:
Chikako Senju, Yuka Nakazawa, Taichi Oso, Mayuko Shimada, Kana Kato, Michiko Matsuse, Mariko Tsujimoto, Taro Masaki, Yasushi Miyazaki, Satoshi Fukushima, Satoshi Tateishi, Atsushi Utani, Hiroyuki Murota, Katsumi Tanaka, Norisato Mitsutake, Shinichi Moriwaki, Chikako Nishigori, Tomoo Ogi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 7/4/2023, Vol. 120 Issue 27, p1-12, 24p
Autor:
Mariko Tsujimoto, Yasumasa Kakei, Nozomi Yamano, Takeshi Fujita, Takehiro Ueda, Ryusuke Ono, Sae Murakami, Shinichi Moriwaki, Chikako Nishigori
Publikováno v:
BMJ Open. 13:e068112
IntroductionXeroderma pigmentosum (XP) is a rare intractable disease without a fundamental treatment, presenting with severe photosensitivity, freckle-like pigmented and depigmented maculae and numerous skin cancers before the age of 10 years without
Publikováno v:
Neurology. 99(14)
We describe the case of a 60-year-old man with a 16-year history of gait imbalance and a 15-year history of forgetfulness. The insidious onset and slow progression suggested that the disease was degenerative. Neurologic examination revealed cerebella
Autor:
Taro Masaki, Mariko Tsujimoto, Riko Kitazawa, Yoko Funasaka, Sohei Kitazawa, Chikako Nishigori, Eiji Nakano, Masamitsu Ichihashi, Akiyoshi Kakita, Fumio Kanda
Publikováno v:
JAAD Case Reports
Xeroderma pigmentosum (XP) is an autosomal recessive disease characterized by abnormally accelerated photoaging skin symptoms for the patient's age caused by failure to repair DNA lesions damaged by ultraviolet radiation.1 Two sibling cases of Japane
Autor:
Yoshiko Oda, Atsushi Fukunaga, Mariko Tsujimoto, Mayumi Hatakeyama, Ken Washio, Chikako Nishigori
Publikováno v:
Allergology International, Vol 64, Iss 2, Pp 214-215 (2015)
Externí odkaz:
https://doaj.org/article/0843420753bd40c499b41afc02ad5912
Autor:
Kazumasa Wakamatsu, Shosuke Ito, Taro Masaki, Hiroshi Nagai, Chikako Nishigori, Noriko Goto, Mariko Tsujimoto
Publikováno v:
Experimental Dermatology. 27:754-762
4-(4-Hydroxyphenyl)-2-butanol (rhododendrol, RD), a skin-whitening agent, was reported to cause skin depigmentation in some users, which is attributed to its cytotoxicity to melanocyte. It was reported that cytotoxicity to melanocyte is possibly medi
Publikováno v:
Journal of Investigative Dermatology. 138(2):467-470