Hashimoto T - Search Results

1

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis.

South AP, Ashton GH, Willoughby C, Ellis IH, Bleck O, Hamada T, Mannion G, Wessagowit V, Hashimoto T, Eady RA, McGrath JA. South AP, et al. Among authors: hashimoto t. Br J Dermatol. 2002 Feb;146(2):216-20. doi: 10.1046/j.1365-2133.2002.04638.x. Br J Dermatol. 2002. PMID: 11903230

2

Human monoclonal anti-basement membrane zone antibodies derived from virally transformed lymphocytes of a patient with bullous pemphigoid recognize epitopes associated with hemidesmosomes.

Shimizu H, Hashimoto T, Nishikawa T, Eady RA. Shimizu H, et al. Among authors: hashimoto t. Br J Dermatol. 1991 Mar;124(3):217-20. doi: 10.1111/j.1365-2133.1991.tb00564.x. Br J Dermatol. 1991. PMID: 1708270

3

A typical case of pemphigoid gestationis with a unique pattern of intercellular immunofluorescence.

Vaughan Jones SA, Bhogal BS, Black MM, Clement M, Hashimoto T, Nishikawa T. Vaughan Jones SA, et al. Among authors: hashimoto t. Br J Dermatol. 1997 Feb;136(2):245-8. Br J Dermatol. 1997. PMID: 9068742

4

Cultured Paget cells derived from the involved skin of a patient with extramammary Paget's disease had an extended life span.

Mori O, Karashima T, Matsuo K, Hashimoto T, Katagata Y. Mori O, et al. Among authors: hashimoto t. J Dermatol. 2000 Jan;27(1):60-3. doi: 10.1111/j.1346-8138.2000.tb02121.x. J Dermatol. 2000. PMID: 10692829 No abstract available.

5

A homozygous missense mutation in the cytoplasmic tail of beta4 integrin, G931D, that disrupts hemidesmosome assembly and underlies Non-Herlitz junctional epidermolysis bullosa without pyloric atresia?

Inoue M, Tamai K, Shimizu H, Owaribe K, Nakama T, Hashimoto T, McGrath JA. Inoue M, et al. Among authors: hashimoto t. J Invest Dermatol. 2000 May;114(5):1061-4. doi: 10.1046/j.1523-1747.2000.00960-3.x. J Invest Dermatol. 2000. PMID: 10792571 Free article. No abstract available.

6

Bullous pemphigoid sera react specifically with various domains of BP230, most frequently with C-terminal domain, by immunoblot analyses using bacterial recombinant proteins covering the entire molecule.

Hamada T, Nagata Y, Tomita M, Salmhofer W, Hashimoto T. Hamada T, et al. Among authors: hashimoto t. Exp Dermatol. 2001 Aug;10(4):256-63. doi: 10.1034/j.1600-0625.2001.100405.x. Exp Dermatol. 2001. PMID: 11493314

7

Genotype-phenotype correlation in skin fragility-ectodermal dysplasia syndrome resulting from mutations in plakophilin 1.

Hamada T, South AP, Mitsuhashi Y, Kinebuchi T, Bleck O, Ashton GH, Hozumi Y, Suzuki T, Hashimoto T, Eady RA, McGrath JA. Hamada T, et al. Among authors: hashimoto t. Exp Dermatol. 2002 Apr;11(2):107-14. doi: 10.1034/j.1600-0625.2002.110202.x. Exp Dermatol. 2002. PMID: 11994137

8

Psoriasis bullosa acquisita.

Morris SD, Mallipeddi R, Oyama N, Gratian MJ, Harman KE, Bhogal BS, Black MM, Eady RA, Hashimoto T, McGrath JA. Morris SD, et al. Among authors: hashimoto t. Clin Exp Dermatol. 2002 Nov;27(8):665-9. doi: 10.1046/j.1365-2230.2002.01100.x. Clin Exp Dermatol. 2002. PMID: 12472542

9

The P25L mutation in the KRT5 gene in a Japanese family with epidermolysis bullosa simplex with mottled pigmentation.

Hamada T, Ishii N, Kawano Y, Takahashi Y, Inoue M, Yasumoto S, Hashimoto T. Hamada T, et al. Among authors: hashimoto t. Br J Dermatol. 2004 Mar;150(3):609-11. doi: 10.1046/j.1365-2133.2004.05820.x. Br J Dermatol. 2004. PMID: 15030360 No abstract available.

10

A Japanese case of dermatitis herpetiformis with facial and palmar lesions.

Hamada T, Hashimoto T. Hamada T, et al. Among authors: hashimoto t. Clin Exp Dermatol. 2005 May;30(3):298-300. doi: 10.1111/j.1365-2230.2005.01739.x. Clin Exp Dermatol. 2005. PMID: 15807697 No abstract available.

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