Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Satoru Shinkuma"'
Autor:
Tatsuya Katsumi, MD, Ryota Hayashi, MD, PhD, Shingo Takei, MD, Rei Yokoyama, MD, Osamu Ansai, MD, PhD, Satoru Shinkuma, MD, PhD, Riichiro Abe, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 46, Iss , Pp 8-10 (2024)
Externí odkaz:
https://doaj.org/article/8e8fb26891964899bee54c401c4b00c1
Autor:
Hong Ha Nguyen, Satoru Shinkuma, Ryota Hayashi, Tatsuya Katsumi, Tomoki Nishiguchi, Ken Natsuga, Yasuyuki Fujita, Riichiro Abe
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 5, Iss 3, Pp 78-87 (2022)
Abstract Objectives Epidermolysis bullosa (EB) is a hereditary disorder characterized by mechanical stress‐induced blistering. The presence of extracutaneous complications such as cardiomyopathy and renal disease observed in severe EB subtypes and
Externí odkaz:
https://doaj.org/article/1851be83fdce4d5282b67b2478ea0cff
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 9, p adv00547 (2021)
Externí odkaz:
https://doaj.org/article/dd784cef46644e4da13688d4f55eed19
Autor:
Akimasa Saito, Yoshiyuki Nakamura, Ryota Tanaka, Sae Inoue, Naoko Okiyama, Yosuke Ishitsuka, Hiroshi Maruyama, Rei Watanabe, Kenji Yoshida, Akira Ishiko, Manabu Fujimoto, Satoru Shinkuma, Yasuhiro Fujisawa
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1166-1169 (2019)
Some bone lesions are reported to mimic bone metastasis on imaging tests. Herein, we report a case of a 55-year-old Japanese man who presented with a skin tumor on the left lower extremity. He also had a history of recurrent generalized cutaneous bli
Externí odkaz:
https://doaj.org/article/389858e1d13e4efcba940ceb8547900d
Autor:
Satoru Shinkuma, Hideki Nakamura, Manami Maehara, Shota Takashima, Toshifumi Nomura, Yasuyuki Fujita, Satoshi Hasegawa, Kazuko C. Sato-Matsumura, Riichiro Abe, Hiroshi Shimizu
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 12, Pp 1110-1115 (2019)
Nail-patella syndrome is an autosomal dominant disorder characterized by nail dysplasia and skeletal anomaly. Some patients have been shown to have ultrastructural abnormalities of the glomerular basement membrane that result in nephrosis. However, l
Externí odkaz:
https://doaj.org/article/fb06c7581dd3427a82c2b1e6c375d5af
Autor:
Kanade Shimada, Ryota Hayashi, Rei Yokoyama, Osamu Ansai, Satoru Shinkuma, Yutaka Shimomura, Riichiro Abe
Publikováno v:
Indian Journal of Dermatology, Vol 67, Iss 1, Pp 94-94 (2022)
Externí odkaz:
https://doaj.org/article/af9392e212c24a6f848cbe3b7672cb22
Autor:
Mika Watanabe, Ken Natsuga, Wataru Nishie, Yasuaki Kobayashi, Giacomo Donati, Shotaro Suzuki, Yu Fujimura, Tadasuke Tsukiyama, Hideyuki Ujiie, Satoru Shinkuma, Hideki Nakamura, Masamoto Murakami, Michitaka Ozaki, Masaharu Nagayama, Fiona M Watt, Hiroshi Shimizu
Publikováno v:
eLife, Vol 6 (2017)
Type XVII collagen (COL17) is a transmembrane protein located at the epidermal basement membrane zone. COL17 deficiency results in premature hair aging phenotypes and in junctional epidermolysis bullosa. Here, we show that COL17 plays a central role
Externí odkaz:
https://doaj.org/article/de5c2abe4d95455fbf4741ece7554610
Publikováno v:
Case Reports in Dermatology, Vol 4, Iss 1, Pp 37-40 (2012)
Cilia are normally found at the eyelid margin, while ectopic cilia are one or more lash follicles appearing in an abnormal position within the eyelid. We herein report two cases of cilia located in the palpebral conjunctiva. A 31-year-old female and
Externí odkaz:
https://doaj.org/article/52af3904bd184127aa4ef8f4c3958d70
Autor:
Kazuhiro Kikuchi, Riichiro Abe, Satoru Shinkuma, Erika Hamasaka, Ken Natsuga, Hiroo Hata, Yasuki Tateishi, Masahiko Shibata, Yuki Tomita, Yukiko Abe, Satoru Aoyagi, Makio Mukai, Hiroshi Shimizu
Publikováno v:
Case Reports in Dermatology, Vol 3, Iss 2, Pp 181-185 (2011)
Infantile myofibromatosis is a rare fibrous tumor of infancy. The cutaneous solitary type has typically an excellent prognosis. However, histologically, it is important to rule out leiomyosarcoma, which has a poor prognosis. The low frequency of mito
Externí odkaz:
https://doaj.org/article/ac841b1140cc45d8845da4a8e314abdb
Autor:
Osamu Ansai, Toshinari Miyauchi, Ryota Hayashi, Tatsuya Katsumi, Tomoki Nishiguchi, Akito Hasegawa, Satoru Shinkuma, Ken Natsuga, Toshifumi Nomura, Yutaka Shimomura, Riichiro Abe
Publikováno v:
Clinical and Experimental Dermatology. 48:199-210
BackgroundEpidermolytic ichthyosis (EI) is a major form of nonsyndromic inherited ichthyosis, characterized by erythroderma, marked hyperkeratosis and scale, bulla and erosion at birth, associated with KRT1/KRT10 mutations. The cytokine and chemokine