Umegaki-Arao N - Search Results

1

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5.

Kumagai Y, Umegaki-Arao N, Sasaki T, Nakamura Y, Takahashi H, Ashida A, Tsunemi Y, Kawashima M, Shimizu A, Ishiko A, Nakamura K, Tsuchihashi H, Amagai M, Kubo A. Kumagai Y, et al. J Eur Acad Dermatol Venereol. 2017 May;31(5):e241-e243. doi: 10.1111/jdv.14005. Epub 2016 Nov 2. J Eur Acad Dermatol Venereol. 2017. PMID: 27730678 No abstract available.

2

Case of dominant dystrophic epidermolysis bullosa with amniotic band syndrome.

Sakiyama T, Umegaki-Arao N, Sasaki T, Kosaki K, Amagai M, Kubo A. Sakiyama T, et al. J Dermatol. 2017 Jan;44(1):102-103. doi: 10.1111/1346-8138.13449. Epub 2016 Apr 30. J Dermatol. 2017. PMID: 27130450 No abstract available.

3

Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A LIPH mutation.

Kinoshita-Ise M, Kubo A, Sasaki T, Umegaki-Arao N, Amagai M, Ohyama M. Kinoshita-Ise M, et al. Br J Dermatol. 2017 Jan;176(1):138-144. doi: 10.1111/bjd.14836. Epub 2016 Dec 19. Br J Dermatol. 2017. PMID: 27375176

4

Case of lymphoplasmacytic plaque in children: Analysis of the distribution of infiltrating immune cells.

Mukai M, Tanese K, Umegaki-Arao N, Kubo A, Takahashi H, Amagai M. Mukai M, et al. J Dermatol. 2016 Nov;43(11):1368-1370. doi: 10.1111/1346-8138.13413. Epub 2016 Apr 14. J Dermatol. 2016. PMID: 27075391 No abstract available.

5

A nonepidermolytic keratinocytic epidermal naevus associated with a postzygotic mutation in the gene encoding epidermal growth factor receptor.

Umegaki-Arao N, Ono N, Tanaka R, Sasaki T, Fujita H, Shiohama A, Aoki S, Amagai M, Kubo A. Umegaki-Arao N, et al. Br J Dermatol. 2020 May;182(5):1303-1305. doi: 10.1111/bjd.18729. Epub 2019 Dec 26. Br J Dermatol. 2020. PMID: 31745974 No abstract available.

6

Inflammatory Linear Verrucous Epidermal Nevus with a Postzygotic GJA1 Mutation Is a Mosaic Erythrokeratodermia Variabilis et Progressiva.

Umegaki-Arao N, Sasaki T, Fujita H, Aoki S, Kameyama K, Amagai M, Seishima M, Kubo A. Umegaki-Arao N, et al. J Invest Dermatol. 2017 Apr;137(4):967-970. doi: 10.1016/j.jid.2016.11.016. Epub 2016 Nov 24. J Invest Dermatol. 2017. PMID: 27890787 Free article. No abstract available.

7

Linear keratinocytic epidermal nevi on trunk skin caused by a somatic FGFR2 p.C382R mutation.

Tanaka R, Umegaki-Arao N, Sasaki T, Aoki S, Yoshida K, Niizeki H, Kubo A. Tanaka R, et al. J Dermatol. 2018 Nov;45(11):e302-e303. doi: 10.1111/1346-8138.14344. Epub 2018 Apr 27. J Dermatol. 2018. PMID: 29701304 No abstract available.

8

Identification of a human papillomavirus type 58 lineage in multiple Bowen's disease on the fingers: Case report and published work review.

Kobayashi K, Tanese K, Kubo A, Matsumoto-Mochimaru N, Sasaki A, Kameyama K, Amagai M, Umegaki-Arao N. Kobayashi K, et al. J Dermatol. 2018 Oct;45(10):1195-1198. doi: 10.1111/1346-8138.14574. Epub 2018 Jul 23. J Dermatol. 2018. PMID: 30035309 Review.

9

Palmar whitish change after water exposure in a familial mild case of loricrin keratoderma (loricrin ichthyosis).

Saito S, Tanaka R, Ono N, Umegaki-Arao N, Sasaki T, Aoki S, Amagai M, Kubo A. Saito S, et al. Among authors: umegaki arao n. J Dermatol. 2022 Nov;49(11):e405-e406. doi: 10.1111/1346-8138.16481. Epub 2022 Jun 3. J Dermatol. 2022. PMID: 35665529 No abstract available.

10

Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosis.

Honda A, Umegaki-Arao N, Sasaki T, Nakabayashi K, Hata K, Matsubara Y, Tanikawa A, Amagai M, Kubo A. Honda A, et al. J Dermatol. 2017 Jun;44(6):e109-e110. doi: 10.1111/1346-8138.13801. Epub 2017 Mar 11. J Dermatol. 2017. PMID: 28295558 No abstract available.

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