Nomura T - Search Results

1

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. J Invest Dermatol. 2009 May;129(5):1302-5. doi: 10.1038/jid.2008.372. Epub 2008 Nov 27. J Invest Dermatol. 2009. PMID: 19037238 Free article. No abstract available.

2

Association of infantile cutaneous haemangioma on the face and neck with respiratory distress in infancy.

Nomura T, Akiyama M, Kikuchi T, Kashiwamura M, Shimizu H. Nomura T, et al. Acta Derm Venereol. 2004;84(1):72-3. doi: 10.1080/00015550310005816. Acta Derm Venereol. 2004. PMID: 15040485 Free article. No abstract available.

3

Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, Ota M, Sugiura H, Yamamoto K, Sato H, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. J Allergy Clin Immunol. 2007 Feb;119(2):434-40. doi: 10.1016/j.jaci.2006.12.646. J Allergy Clin Immunol. 2007. PMID: 17291859

4

Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan.

Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Ota M, Hata H, Evans AT, Palmer CN, Shimizu H, McLean WH. Nomura T, et al. J Invest Dermatol. 2008 Jun;128(6):1436-41. doi: 10.1038/sj.jid.5701205. Epub 2008 Jan 17. J Invest Dermatol. 2008. PMID: 18200065 Free article.

5

Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation.

Tsubota A, Akiyama M, Kanitakis J, Sakai K, Nomura T, Claudy A, Shimizu H. Tsubota A, et al. Among authors: nomura t. J Invest Dermatol. 2008 Jul;128(7):1648-52. doi: 10.1038/sj.jid.5701257. Epub 2008 Jan 24. J Invest Dermatol. 2008. PMID: 18219278 Free article.

6

Papuloerythroderma of Ofuji associated with early gastric cancer.

Nomura T, Kodama K, Moriuchi R, Yaosaka M, Kawasaki H, Abe M, Sawamura D, Shimizu H. Nomura T, et al. Int J Dermatol. 2008 Jun;47(6):590-1. doi: 10.1111/j.1365-4632.2008.03635.x. Int J Dermatol. 2008. PMID: 18477151 No abstract available.

7

Clinical severity correlates with impaired barrier in filaggrin-related eczema.

Nemoto-Hasebe I, Akiyama M, Nomura T, Sandilands A, McLean WH, Shimizu H. Nemoto-Hasebe I, et al. Among authors: nomura t. J Invest Dermatol. 2009 Mar;129(3):682-9. doi: 10.1038/jid.2008.280. Epub 2008 Sep 25. J Invest Dermatol. 2009. PMID: 18818676 Free article.

8

Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.

Shinkuma S, Akiyama M, Inoue A, Aoki J, Natsuga K, Nomura T, Arita K, Abe R, Ito K, Nakamura H, Ujiie H, Shibaki A, Suga H, Tsunemi Y, Nishie W, Shimizu H. Shinkuma S, et al. Among authors: nomura t. Hum Mutat. 2010 May;31(5):602-10. doi: 10.1002/humu.21235. Hum Mutat. 2010. PMID: 20213768

9

Chromosome 11q13.5 variant: No association with atopic eczema in the Japanese population.

Nomura Y, Akiyama M, Nomura T, Nemoto-Hasebe I, Abe R, McLean WH, Shimizu H. Nomura Y, et al. Among authors: nomura t. J Dermatol Sci. 2010 Sep;59(3):210-2. doi: 10.1016/j.jdermsci.2010.06.010. Epub 2010 Jul 7. J Dermatol Sci. 2010. PMID: 20656460 No abstract available.

10

Japanese-specific filaggrin gene mutations in Japanese patients suffering from atopic eczema and asthma.

Osawa R, Konno S, Akiyama M, Nemoto-Hasebe I, Nomura T, Nomura Y, Abe R, Sandilands A, McLean WH, Hizawa N, Nishimura M, Shimizu H. Osawa R, et al. Among authors: nomura t, nomura y. J Invest Dermatol. 2010 Dec;130(12):2834-6. doi: 10.1038/jid.2010.218. Epub 2010 Aug 5. J Invest Dermatol. 2010. PMID: 20686498 Free article. No abstract available.

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