Suganuma M - Search Results

1

Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.

Kono M, Sugiura K, Suganuma M, Hayashi M, Takama H, Suzuki T, Matsunaga K, Tomita Y, Akiyama M. Kono M, et al. Among authors: suganuma m. Hum Mol Genet. 2013 Sep 1;22(17):3524-33. doi: 10.1093/hmg/ddt207. Epub 2013 May 10. Hum Mol Genet. 2013. PMID: 23666529

2

Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.

Kono M, Suganuma M, Takama H, Zarzoso I, Saritha M, Bodet D, Aboobacker S, Kaliaperumal K, Suzuki T, Tomita Y, Sugiura K, Akiyama M. Kono M, et al. Among authors: suganuma m. Br J Dermatol. 2015 Aug;173(2):584-6. doi: 10.1111/bjd.13702. Epub 2015 Jun 29. Br J Dermatol. 2015. PMID: 25639155 No abstract available.

3

Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families.

Kono M, Suganuma M, Akiyama M, Ito Y, Ujiie H, Morimoto K. Kono M, et al. Among authors: suganuma m. Int J Dermatol. 2014 Mar;53(3):e194-6. doi: 10.1111/j.1365-4632.2012.05765.x. Epub 2013 Apr 28. Int J Dermatol. 2014. PMID: 23621649 No abstract available.

4

Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?

Kono M, Akiyama M, Suganuma M, Tomita Y, Sanchez-Valle A. Kono M, et al. Among authors: suganuma m. Int J Dermatol. 2013 Dec;52(12):1582-4. doi: 10.1111/j.1365-4632.2011.05372.x. Int J Dermatol. 2013. PMID: 24261734 No abstract available.

5

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.

Kono M, Matsumoto F, Suzuki Y, Suganuma M, Saitsu H, Ito Y, Fujiwara S, Moriwaki S, Matsumoto K, Matsumoto N, Tomita Y, Sugiura K, Akiyama M. Kono M, et al. Among authors: suganuma m. J Invest Dermatol. 2016 Apr;136(4):875-878. doi: 10.1016/j.jid.2015.12.034. Epub 2016 Jan 21. J Invest Dermatol. 2016. PMID: 26802932 Free article. No abstract available.

6

Pathogenesis of a variant in the 5' untranslated region of ADAR1 in dyschromatosis symmetrica hereditaria.

Suganuma M, Kono M, Yamanaka M, Akiyama M. Suganuma M, et al. Pigment Cell Melanoma Res. 2020 Jul;33(4):591-600. doi: 10.1111/pcmr.12863. Epub 2020 Jan 27. Pigment Cell Melanoma Res. 2020. PMID: 31926050

7

Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria.

Kobayashi T, Kono M, Suganuma M, Akita H, Takai A, Tsutsui K, Inasaka Y, Takeichi T, Muro Y, Akiyama M. Kobayashi T, et al. Among authors: suganuma m. Nagoya J Med Sci. 2018 May;80(2):267-277. doi: 10.18999/nagjms.80.2.267. Nagoya J Med Sci. 2018. PMID: 29915444 Free PMC article.

8

Homozygous variant p.Ser427Pro in PNPLA1 is a preventive factor from atopic dermatitis.

Watanabe N, Kono M, Suganuma M, Tanahashi K, Akiyama M. Watanabe N, et al. Among authors: suganuma m. J Dermatol Sci. 2020 Jan;97(1):86-88. doi: 10.1016/j.jdermsci.2019.12.006. Epub 2019 Dec 12. J Dermatol Sci. 2020. PMID: 31864761 No abstract available.

9

Multifaceted Analyses of Epidermal Serine Protease Activity in Patients with Atopic Dermatitis.

Nomura H, Suganuma M, Takeichi T, Kono M, Isokane Y, Sunagawa K, Kobashi M, Sugihara S, Kajita A, Miyake T, Hirai Y, Yamasaki O, Akiyama M, Morizane S. Nomura H, et al. Among authors: suganuma m. Int J Mol Sci. 2020 Jan 30;21(3):913. doi: 10.3390/ijms21030913. Int J Mol Sci. 2020. PMID: 32019242 Free PMC article.

10

Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression.

Kono M, Suganuma M, Dutta A, Ghosh SK, Takeichi T, Muro Y, Akiyama M. Kono M, et al. Among authors: suganuma m. Br J Dermatol. 2018 Aug;179(2):509-511. doi: 10.1111/bjd.16610. Epub 2018 May 29. Br J Dermatol. 2018. PMID: 29603717 No abstract available.

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