Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Katuto, Tamai"'
Autor:
Takashi Hashimoto, Hiroshi Koga, Sachiko Sakaguchi, Norito Ishii, Hajime Nakano, Shunpei Fukuda, Takahiro Hamada, Daisuke Sawamura, Katuto Tamai
Publikováno v:
The Journal of Dermatology. 38:489-492
Dystrophic epidermolysis bullosa (DEB) is a rare, inherited, blistering disorder resulting from mutations in the COL7A1 gene, which encodes the anchoring fibrils, type VII collagen. We herein describe a further Japanese girl diagnosed with dominant D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::957ce5672601036e4219af821dccb0ca
https://doi.org/10.1111/j.1346-8138.2010.01008.x
https://doi.org/10.1111/j.1346-8138.2010.01008.x
Autor:
Masafumi, Ohashi, En, Shu, Miki, Nagai, Kana, Murase, Hajime, Nakano, Katuto, Tamai, Daisuke, Sawamura, Takako, Hiroka, Mariko, Seishima, Yasuo, Kitajima, Yumi, Aoyama
Publikováno v:
The Journal of dermatology. 38(9)
Recessive dystrophic epidermolysis bullosa (RDEB) is a congenital bullous disease resulting from defective anchoring fibrils at the dermal-epidermal junction and mutations in the type VII collagen gene. In this report, we describe two patients with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db402b44414b65970bdc75c16b7f8b92
https://pubmed.ncbi.nlm.nih.gov/21658117
https://pubmed.ncbi.nlm.nih.gov/21658117
Autor:
Takako Hiroka, Masafumi Ohashi, Hajime Nakano, Kana Murase, En Shu, Miki Nagai, Daisuke Sawamura, Yumi Aoyama, Mariko Seishima, Yasuo Kitajima, Katuto Tamai
Publikováno v:
The Journal of Dermatology.
Recessive dystrophic epidermolysis bullosa (RDEB) is a congenital bullous disease resulting from defective anchoring fibrils at the dermal-epidermal junction and mutations in the type VII collagen gene. In this report, we describe two patients with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42df43007f20305e4c21b022f671fd26
https://doi.org/10.1111/j.1346-8138.2011.01230.x
https://doi.org/10.1111/j.1346-8138.2011.01230.x
Autor:
Hiroshi, Koga, Takahiro, Hamada, Norito, Ishii, Shunpei, Fukuda, Sachiko, Sakaguchi, Hajime, Nakano, Katuto, Tamai, Daisuke, Sawamura, Takashi, Hashimoto
Publikováno v:
The Journal of dermatology. 38(5)
Dystrophic epidermolysis bullosa (DEB) is a rare, inherited, blistering disorder resulting from mutations in the COL7A1 gene, which encodes the anchoring fibrils, type VII collagen. We herein describe a further Japanese girl diagnosed with dominant D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f44945a195d2fda23d52948c4e596dfd
https://pubmed.ncbi.nlm.nih.gov/21352278
https://pubmed.ncbi.nlm.nih.gov/21352278