Yasuda M - Search Results

1

Autosomal dominant familial acanthosis nigricans caused by a C-terminal nonsense mutation of FGFR3.

Tahara U, Yasuda M, Yamada Y, Aoki S, Sato S, Amagai M, Kubo A. Tahara U, et al. Among authors: yasuda m. J Hum Genet. 2021 Aug;66(8):831-834. doi: 10.1038/s10038-021-00905-1. Epub 2021 Feb 12. J Hum Genet. 2021. PMID: 33580140

2

Familial acanthosis nigricans with the FGFR3 mutation: Differences of pigmentation between male and female patients.

Yasuda M, Morimoto N, Shimizu A, Toyoshima T, Yokoyama Y, Ishikawa O. Yasuda M, et al. J Dermatol. 2018 Nov;45(11):1357-1361. doi: 10.1111/1346-8138.14623. Epub 2018 Aug 31. J Dermatol. 2018. PMID: 30168875

3

Case of X-linked hypohidrotic ectodermal dysplasia with a novel EDA missense mutation.

Yasuda M, Kishi C, Yokoyama Y, Amano H, Ishikawa O. Yasuda M, et al. J Dermatol. 2015 Sep;42(9):907-8. doi: 10.1111/1346-8138.12959. Epub 2015 Jun 5. J Dermatol. 2015. PMID: 26046476 No abstract available.

4

In-frame Val²¹⁶-Ser²¹⁷ deletion of KIT in mild piebaldism causes aberrant secretion and SCF response.

Hattori M, Ishikawa O, Oikawa D, Amano H, Yasuda M, Kaira K, Ishida-Yamamoto A, Nakano H, Sawamura D, Terawaki SI, Wakamatsu K, Tokunaga F, Shimizu A. Hattori M, et al. Among authors: yasuda m. J Dermatol Sci. 2018 Jul;91(1):35-42. doi: 10.1016/j.jdermsci.2018.03.012. Epub 2018 Mar 21. J Dermatol Sci. 2018. PMID: 29631773

5

Cutaneous squamous cell carcinoma, thyroid cancer and Langerhans cell histiocytosis in a patient with X-linked recessive Mendelian susceptibility to mycobacterial diseases with a nuclear factor-κB essential modifier mutation.

Inoue Y, Shimizu A, Suto M, Kishi C, Takahashi A, Yasuda M, Iijima M, Arakawa H, Ishikawa O. Inoue Y, et al. Among authors: yasuda m. J Dermatol. 2018 Aug;45(8):1017-1019. doi: 10.1111/1346-8138.14482. Epub 2018 May 24. J Dermatol. 2018. PMID: 29797522

6

Focal palmoplantar keratoderma in a patient with the KRT6B mutation.

Kuriyama Y, Shimizu A, Kanai S, Yokoyama Y, Yasuda M, Endo Y, Kawabata-Iwakawa R, Motegi SI. Kuriyama Y, et al. Among authors: yasuda m. J Dermatol. 2022 Mar;49(3):e111-e112. doi: 10.1111/1346-8138.16251. Epub 2021 Nov 19. J Dermatol. 2022. PMID: 34796977 No abstract available.

7

Novel mutation in COL7A1 in recessive dystrophic epidermolysis bullosa successfully treated with cultured epidermal autograft transplantation.

Kuriyama Y, Shimizu A, Kosaka K, Yasuda M, Shinkuma S, Ishikawa O, Motegi SI. Kuriyama Y, et al. Among authors: yasuda m. J Dermatol. 2021 Sep;48(9):e480-e481. doi: 10.1111/1346-8138.16029. Epub 2021 Jun 19. J Dermatol. 2021. PMID: 34145917 No abstract available.

8

Clinical course and background of eight patients who discontinued secukinumab after achieving a score of 0 on the psoriasis area and severity index.

Yasuda M, Morimoto N, Inoue Y, Ishikawa O, Motegi SI. Yasuda M, et al. J Dermatol. 2021 Aug;48(8):e380-e381. doi: 10.1111/1346-8138.15948. Epub 2021 May 18. J Dermatol. 2021. PMID: 34002889 No abstract available.

9

Calciphylaxis and nephrogenic fibrosing dermopathy with pseudoxanthoma elasticum-like changes: Successful treatment with sodium thiosulfate.

Ishikawa M, Motegi SI, Toki S, Endo Y, Yasuda M, Ishikawa O. Ishikawa M, et al. Among authors: yasuda m. J Dermatol. 2019 Jul;46(7):e240-e242. doi: 10.1111/1346-8138.14780. Epub 2019 Jan 21. J Dermatol. 2019. PMID: 30663093 No abstract available.

10

Detection of human papillomavirus type 16 in digital squamous cell carcinoma.

Kuriyama Y, Shimizu A, Kanai S, Kim J, Yasuda M, Ishikawa O. Kuriyama Y, et al. Among authors: yasuda m. J Dermatol. 2020 Jun;47(6):e234-e235. doi: 10.1111/1346-8138.15342. Epub 2020 Apr 7. J Dermatol. 2020. PMID: 32255533 No abstract available.

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