Ishiko A - Search Results

1

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.

Sasaki T, Niizeki H, Shimizu A, Shiohama A, Hirakiyama A, Okuyama T, Seki A, Kabashima K, Otsuka A, Ishiko A, Tanese K, Miyakawa S, Sakabe J, Kuwahara M, Amagai M, Okano H, Suematsu M, Kudoh J. Sasaki T, et al. Among authors: ishiko a. J Dermatol Sci. 2012 Oct;68(1):36-44. doi: 10.1016/j.jdermsci.2012.07.008. Epub 2012 Jul 27. J Dermatol Sci. 2012. PMID: 22906430

2

Classic (non-AIDS-related) Kaposi's sarcoma in a Japanese patient, successfully treated with alpha-2b-interferon.

Shimizu S, Tanaka M, Niizeki H, Miyakawa S, Ishiko A, Shimizu H. Shimizu S, et al. Among authors: ishiko a. Br J Dermatol. 1995 Aug;133(2):332-4. doi: 10.1111/j.1365-2133.1995.tb02646.x. Br J Dermatol. 1995. PMID: 7547414 Review. No abstract available.

3

A Japanese case of the fibrillar type of dermatitis herpetiformis.

Shimizu K, Hashimoto T, Fukuda T, Watanabe K, Ishiko A, Niizeki H, Shimizu H, Zone JJ, Nishikawa T. Shimizu K, et al. Among authors: ishiko a. Dermatology. 1995;191(2):88-92. doi: 10.1159/000246522. Dermatology. 1995. PMID: 8520073

4

Ultrastructural changes in mice actively producing antibodies to desmoglein 3 parallel those in patients with pemphigus vulgaris.

Shimizu A, Ishiko A, Ota T, Tsunoda K, Koyasu S, Amagai M, Nishikawa T. Shimizu A, et al. Among authors: ishiko a. Arch Dermatol Res. 2002 Oct;294(7):318-23. doi: 10.1007/s00403-002-0341-z. Epub 2002 Sep 5. Arch Dermatol Res. 2002. PMID: 12373337

5

Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations.

Murata T, Masunaga T, Ishiko A, Shimizu H, Nishikawa T. Murata T, et al. Among authors: ishiko a. Arch Dermatol Res. 2004 Mar;295(10):442-7. doi: 10.1007/s00403-003-0444-1. Epub 2004 Jan 16. Arch Dermatol Res. 2004. PMID: 14727126

6

IgG binds to desmoglein 3 in desmosomes and causes a desmosomal split without keratin retraction in a pemphigus mouse model.

Shimizu A, Ishiko A, Ota T, Tsunoda K, Amagai M, Nishikawa T. Shimizu A, et al. Among authors: ishiko a. J Invest Dermatol. 2004 May;122(5):1145-53. doi: 10.1111/j.0022-202X.2004.22426.x. J Invest Dermatol. 2004. PMID: 15140217 Free article.

7

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephaloapthy (CADASIL): a hereditary cerebrovascular disease, which can be diagnosed by skin biopsy electron microscopy.

Ishiko A, Shimizu A, Nagata E, Ohta K, Tanaka M. Ishiko A, et al. Am J Dermatopathol. 2005 Apr;27(2):131-4. doi: 10.1097/01.dad.0000136691.96212.ec. Am J Dermatopathol. 2005. PMID: 15798438

8

In vivo ultrastructural localization of the desmoglein 3 adhesive interface to the desmosome mid-line.

Shimizu A, Ishiko A, Ota T, Saito H, Oka H, Tsunoda K, Amagai M, Nishikawa T. Shimizu A, et al. Among authors: ishiko a. J Invest Dermatol. 2005 May;124(5):984-9. doi: 10.1111/j.0022-202X.2005.23706.x. J Invest Dermatol. 2005. PMID: 15854040 Free article.

9

Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL.

Ishiko A, Shimizu A, Nagata E, Takahashi K, Tabira T, Suzuki N. Ishiko A, et al. Acta Neuropathol. 2006 Sep;112(3):333-9. doi: 10.1007/s00401-006-0116-2. Epub 2006 Jul 27. Acta Neuropathol. 2006. PMID: 16871402

10

Novel mutation of the Notch3 gene in a Japanese patient with CADASIL.

Oki K, Nagata E, Ishiko A, Shimizu A, Tanaka K, Takahashi K, Tabira T, Katayama T, Suzuki N. Oki K, et al. Among authors: ishiko a. Eur J Neurol. 2007 Apr;14(4):464-6. doi: 10.1111/j.1468-1331.2007.01641.x. Eur J Neurol. 2007. PMID: 17389000

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