Toyomaki Y - Search Results

1

Novel COL7A1 mutations in a Japanese family with transient bullous dermolysis of the newborn associated with pseudosyndactyly.

Nakano H, Toyomaki Y, Ohashi S, Nakano A, Jin H, Munakata T, Akita N, Tamai K, Mitsuhashi Y. Nakano H, et al. Among authors: toyomaki y. Br J Dermatol. 2007 Jul;157(1):179-82. doi: 10.1111/j.1365-2133.2007.07955.x. Epub 2007 May 14. Br J Dermatol. 2007. PMID: 17501948 No abstract available.

2

A novel H1 domain mutation in the keratin 2 gene in a Japanese family with ichthyosis bullosa of Siemens.

Nishizawa A, Toyomaki Y, Nakano A, Takeuchi S, Matsuzaki Y, Takeda H, Kaneko T, Mitsuhashi Y, Nakano H. Nishizawa A, et al. Among authors: toyomaki y. Br J Dermatol. 2007 May;156(5):1042-4. doi: 10.1111/j.1365-2133.2007.07832.x. Epub 2007 Apr 4. Br J Dermatol. 2007. PMID: 17408392 No abstract available.

3

Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1).

Iwata T, Nakano H, Nakano A, Toyomaki Y, Tamai K, Tomita Y. Iwata T, et al. Among authors: toyomaki y. J Dermatol. 2006 Aug;33(8):550-6. doi: 10.1111/j.1346-8138.2006.00130.x. J Dermatol. 2006. PMID: 16923137

4

Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation.

Akasaka E, Nakano H, Nakano A, Toyomaki Y, Takiyoshi N, Rokunohe D, Nishikawa Y, Korekawa A, Matsuzaki Y, Mitsuhashi Y, Sawamura D. Akasaka E, et al. Among authors: toyomaki y. Br J Dermatol. 2011 Dec;165(6):1290-2. doi: 10.1111/j.1365-2133.2011.10552.x. Br J Dermatol. 2011. PMID: 21801157

5

Novel SLC39A4 mutations in acrodermatitis enteropathica.

Nakano A, Nakano H, Nomura K, Toyomaki Y, Hanada K. Nakano A, et al. Among authors: toyomaki y. J Invest Dermatol. 2003 Jun;120(6):963-6. doi: 10.1046/j.1523-1747.2003.12243.x. J Invest Dermatol. 2003. PMID: 12787121 Free article.

6

Novel ferrochelatase mutations in Japanese patients with erythropoietic protoporphyria: high frequency of the splice site modulator IVS3-48C polymorphism in the Japanese population.

Nakano H, Nakano A, Toyomaki Y, Ohashi S, Harada K, Moritsugu R, Takeda H, Kawada A, Mitsuhashi Y, Hanada K. Nakano H, et al. Among authors: toyomaki y. J Invest Dermatol. 2006 Dec;126(12):2717-9. doi: 10.1038/sj.jid.5700456. Epub 2006 Jun 22. J Invest Dermatol. 2006. PMID: 16794582 Free article. No abstract available.

7

Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability.

Akasaka E, Nakano H, Takagi Y, Toyomaki Y, Sawamura D. Akasaka E, et al. Among authors: toyomaki y. Pediatr Dermatol. 2017 Mar;34(2):e106-e108. doi: 10.1111/pde.13047. Epub 2016 Dec 23. Pediatr Dermatol. 2017. PMID: 28008652

8

Calcineurin/NFAT-dependent regulation of 230-kDa bullous pemphigoid antigen (BPAG1) gene expression in normal human epidermal keratinocytes.

Aizu T, Tamai K, Nakano H, Rokunohe D, Toyomaki Y, Uitto J, Sawamura D. Aizu T, et al. Among authors: toyomaki y. J Dermatol Sci. 2008 Jul;51(1):45-51. doi: 10.1016/j.jdermsci.2008.01.006. Epub 2008 Mar 18. J Dermatol Sci. 2008. PMID: 18353617

9

Rubinstein-Taybi syndrome with multiple pilomatricomas: The first case diagnosed by CREBBP mutation analysis.

Rokunohe D, Nakano H, Akasaka E, Toyomaki Y, Sawamura D. Rokunohe D, et al. Among authors: toyomaki y. J Dermatol Sci. 2016 Sep;83(3):240-2. doi: 10.1016/j.jdermsci.2016.06.005. Epub 2016 Jun 7. J Dermatol Sci. 2016. PMID: 27342041 No abstract available.

10

Buschke-Ollendorff syndrome associated with hypertrophic scar formation: a possible role for LEMD3 mutation.

Korekawa A, Nakano H, Toyomaki Y, Takiyoshi N, Rokunohe D, Akasaka E, Nakajima K, Sawamura D. Korekawa A, et al. Among authors: toyomaki y. Br J Dermatol. 2012 Apr;166(4):900-3. doi: 10.1111/j.1365-2133.2011.10691.x. Epub 2012 Jan 9. Br J Dermatol. 2012. PMID: 21985280 No abstract available.

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