Zobrazeno 91 - 100
of 387
pro vyhledávání: '"Hajime Nakano"'
Publikováno v:
British Journal of Dermatology. 174:172-175
Erythropoietic protoporphyria (EPP) is an inherited cutaneous porphyria caused by both the partial deficiency of ferrochelatase (FECH) and the existence of cytosine at IVS3-48 in trans to a mutated FECH allele. However, physicians occasionally encoun
Autor:
Eijiro Akasaka, Hajime Nakano, Ayumi Korekawa, Daiki Rokunohe, Takahide Kaneko, Daisuke Sawamura
Publikováno v:
Case Reports in Dermatology
Case Reports in Dermatology, Vol 7, Iss 3, Pp 292-297 (2015)
Case Reports in Dermatology, Vol 7, Iss 3, Pp 292-297 (2015)
Primary rhabdoid melanoma (PRM) is a rare variant of melanoma. Herein, we describe a case of primary amelanotic rhabdoid melanoma and review the clinicopathological features of previously reported cases of PRMs. A 63-year-old Japanese man presented w
Autor:
Shinichi Moriwaki, Yasuhito Kokunai, Hajime Nakano, Hideaki Tanizaki, Eijiro Akasaka, Yukiko Ninomiya
Publikováno v:
The Journal of Dermatology. 43:414-418
A 12-year-old boy with photosensitivity since 3 years of age presented with small concavities on both cheeks, the nasal root and the dorsal surface of both hands. According to the clinical features, erythropoietic protoporphyria (EPP) was suspected.
Autor:
Tadamichi Shimizu, Hajime Nakano, Megumi Mizawa, Ryotaro Torai, Fumina Furukawa, Daisuke Sawamura, Teruhiko Makino
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 3, Iss 3, Pp 169-171 (2017)
JAAD Case Reports, Vol 3, Iss 3, Pp 169-171 (2017)
Autor:
Kayo Jin, Takahide Aizu, Yasushi Matsuzaki, Koji Nakajima, Takahide Kaneko, Daisuke Sawamura, Hajime Nakano
Publikováno v:
International Journal of Dermatology. 56:e124-e126
Publikováno v:
Scientia Horticulturae. 261:109028
Rapid germination and early establishment of seedlings under unfavorable environmental conditions are desirable traits for seedling production. Quantitative trait locus (QTL) analysis of germination speed was conducted at 15 and 25 °C using a backcr
Publikováno v:
Journal of Dermatological Science. 83:240-242
Autor:
Mai, Hattori, Osamu, Ishikawa, Daisuke, Oikawa, Hiroo, Amano, Masahito, Yasuda, Kyoichi, Kaira, Akemi, Ishida-Yamamoto, Hajime, Nakano, Daisuke, Sawamura, Shin-Ichi, Terawaki, Kaori, Wakamatsu, Fuminori, Tokunaga, Akira, Shimizu
Publikováno v:
Journal of dermatological science. 91(1)
Piebaldism is a pigmentary disorder characterized by a white forelock and depigmented patches. Although the loss-of-function mutations in the KIT gene underlie the disease, the intracellular dynamics of the mutant KIT are largely unknown. We herein r
Publikováno v:
Journal of Cutaneous Immunology and Allergy. 2:62-63
Publikováno v:
Journal of Nippon Medical School = Nippon Ika Daigaku zasshi. 84(5)
Darier disease (DD) is a rare autosomal dominant skin disorder due to mutations in the ATP2A2 gene, which encodes sarco/endoplasmic reticulum Ca