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Items: 1 to 20 of 110

1.

A de novo missense mutation in the keratin 13 gene in oral white sponge naevus.

Nishizawa A, Nakajima R, Nakano H, Sawamura D, Takayama K, Satoh T, Yokozeki H.

Br J Dermatol. 2008 Sep;159(4):974-5. doi: 10.1111/j.1365-2133.2008.08716.x. Epub 2008 Jul 4. No abstract available.

PMID:
18616775
2.

Mutational analysis in familial and sporadic patients with white sponge naevus.

Liu X, Li Q, Gao Y, Song S, Hua H.

Br J Dermatol. 2011 Aug;165(2):448-51. doi: 10.1111/j.1365-2133.2011.10404.x. No abstract available.

PMID:
21561439
3.

Two new mutations in the keratin 4 gene causing oral white sponge nevus in Chinese family.

Zhang JM, Yang ZW, Chen RY, Gao P, Zhang YR, Zhang LF.

Oral Dis. 2009 Jan;15(1):100-5. doi: 10.1111/j.1601-0825.2008.01498.x. Epub 2008 Oct 25.

PMID:
18992023
4.

Constitutional mutation of keratin 13 gene in familial white sponge nevus.

Shibuya Y, Zhang J, Yokoo S, Umeda M, Komori T.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003 Nov;96(5):561-5.

PMID:
14600690
5.

White sponge nevus caused by a missense mutation in the keratin 4 gene.

Shimizu A, Yokoyama Y, Shimomura Y, Ishikawa O.

Eur J Dermatol. 2012 Jul-Aug;22(4):571-2. doi: 10.1684/ejd.2012.1765. No abstract available.

PMID:
22645290
6.

A novel mutation in the keratin 4 gene causing white sponge naevus.

Chao SC, Tsai YM, Yang MH, Lee JY.

Br J Dermatol. 2003 Jun;148(6):1125-8.

PMID:
12828738
7.

Orofacial disease: update for the dental clinical team: 3. White lesions.

Scully C, Porter S.

Dent Update. 1999 Apr;26(3):123-9. Review.

PMID:
10528553
8.

White sponge naevus with minimal clinical and histological changes: report of three cases.

Lucchese A, Favia G.

J Oral Pathol Med. 2006 May;35(5):317-9.

PMID:
16630298
9.

A Japanese patient with a mild form of lamellar ichthyosis harbouring two missense mutations in the core domain of the transglutaminase 1 gene.

Muramatsu S, Suga Y, Kon J, Matsuba S, Hashimoto Y, Ogawa H.

Br J Dermatol. 2004 Feb;150(2):390-2. No abstract available.

PMID:
14996130
10.

White patches on the oral mucosa.

Smillie AC.

N Z Dent J. 1965 Oct;61(286):262-70. No abstract available.

PMID:
5231494
11.

Longitudinal study of TP53 mutations in eight patients with potentially malignant oral mucosal disorders.

Ogmundsdóttir HM, Hilmarsdóttir H, Björnsson J, Holbrook WP.

J Oral Pathol Med. 2009 Oct;38(9):716-21. doi: 10.1111/j.1600-0714.2009.00767.x. Epub 2009 Mar 14.

PMID:
19473449
12.

Oral white sponge naevus: case report.

Iamaroon A, Pongsiriwet S.

Dent Update. 2003 Jun;30(5):252-3.

PMID:
12861763
13.

Expression of Mcm7 and Cdc6 in oral squamous cell carcinoma and precancerous lesions.

Feng CJ, Li HJ, Li JN, Lu YJ, Liao GQ.

Anticancer Res. 2008 Nov-Dec;28(6A):3763-9.

14.

A sporadic case of early-onset sarcoidosis resembling Blau syndrome due to the recurrent R334W missense mutation on the NOD2 gene.

Coto-Segura P, Mallo-Garcia S, Costa-Romero M, Arostegui JI, Yague J, Ramos-Polo E, Santos-Juanes J.

Br J Dermatol. 2007 Dec;157(6):1257-9. Epub 2007 Oct 4.

PMID:
17916199
15.

[White sponge nevus (hereditary leukokeratosis of the mucous membranes)].

Yücel O, Günaydin Y, Sengün O, Gürbüzer B, Günhan O.

Ankara Univ Hekim Fak Derg. 1985 Jan-Apr;12(1):207-12. Turkish. No abstract available.

PMID:
3870096
16.

Mutation M157R of keratin 9 in a Chinese family with epidermolytic palmoplantar keratoderma.

Zhao JJ, Zhang ZH, Niu ZM, Xiang LH, Ye XY, Huang W, Zheng ZZ.

Int J Dermatol. 2008 Jun;47(6):634-7. doi: 10.1111/j.1365-4632.2008.03441.x. No abstract available.

PMID:
18477167
17.

Four novel mutations of the coproporphyrinogen III oxidase gene.

Aurizi C, Lupia Palmieri G, Barbieri L, Macrì A, Sorge F, Usai G, Biolcati G.

Cell Mol Biol (Noisy-le-grand). 2009 Feb 16;55(1):15-8.

PMID:
19267996
18.

A novel keratin 9 gene mutation (Met156Arg) in a Japanese patient with epidermolytic palmoplantar keratoderma.

Shimazu K, Tsunemi Y, Hattori N, Saeki H, Komine M, Adachi M, Tamaki K.

Int J Dermatol. 2006 Sep;45(9):1128-30. No abstract available.

PMID:
16961539
19.

[Mutation analysis of the keratin 9 gene in a pedigree with diffuse epidermolytic plamoplantar keratoderma].

Li M, Zhang GL, Zhai JX, Wei L, Zhu XH, Dai XY, Yang LJ.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):387-9. Chinese.

PMID:
18683133
20.

Genetics of Meesmann corneal dystrophy: a novel mutation in the keratin 3 gene in an asymptomatic family suggests genotype-phenotype correlation.

Szaflik JP, Ołdak M, Maksym RB, Kamińska A, Pollak A, Udziela M, Płoski R, Szaflik J.

Mol Vis. 2008 Sep 15;14:1713-8.

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