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Items: 1 to 20 of 89

1.

Focal palmoplantar keratoderma with epidermolytic degeneration.

Oiso N, Kawara S, Kawada A.

J Eur Acad Dermatol Venereol. 2009 May;23(5):570-1. doi: 10.1111/j.1468-3083.2008.02857.x. Epub 2008 Jun 28. No abstract available.

PMID:
18554216
2.

A family of Unna-Thost disease with one of them showing findings of epidermolytic keratoderma.

Karadag AS, Simsek GG.

Indian J Dermatol Venereol Leprol. 2010 Jan-Feb;76(1):85. doi: 10.4103/0378-6323.58699. No abstract available.

3.

Epidermolytic palmoplantar keratoderma with constriction bands on bilateral fifth toes.

Funakushi N, Mayuzumi N, Sugimura R, Ikeda S.

Arch Dermatol. 2009 May;145(5):609-10. doi: 10.1001/archdermatol.2009.83. No abstract available.

PMID:
19451521
4.

[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma].

Zhang XN, Mao W, He XH, Lai Z.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Aug;21(4):372-5. Review. Chinese.

PMID:
15300637
5.

Case of epidermolytic palmoplantar keratoderma with knuckle pads.

Hayashi M, Nakano H, Sawamura D, Suzuki T.

J Dermatol. 2012 Jan;39(1):84-7. doi: 10.1111/j.1346-8138.2011.01226.x. Epub 2011 Apr 5. No abstract available.

PMID:
21463360
6.

Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred.

Chen XL, Xu CM, Cai SR, Chen CY, Zhang XN.

Prenat Diagn. 2009 Sep;29(9):911-3. doi: 10.1002/pd.2315. No abstract available.

PMID:
19548225
7.

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
8.

A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma.

Bergman R, Khamaysi Z, Sprecher E.

Am J Dermatopathol. 2008 Apr;30(2):101-5. doi: 10.1097/DAD.0b013e3181614898.

PMID:
18360110
9.
10.

A missense mutation in exon 1 of the keratin 9 gene in a Japanese patient with "Vörner type" hereditary palmoplantar keratoderma.

Sakabe J, Nakamura M, Tokura Y.

Eur J Dermatol. 2009 May-Jun;19(3):286-7. doi: 10.1684/ejd.2009.0657. Epub 2009 Mar 3. No abstract available.

PMID:
19258236
11.

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad-like lesions and recurrent mutation causing digital mutilation.

Umegaki N, Nakano H, Tamai K, Mitsuhashi Y, Akasaka E, Sawamura D, Katayama I.

Br J Dermatol. 2011 Jul;165(1):199-201. doi: 10.1111/j.1365-2133.2011.10317.x. No abstract available.

PMID:
21410681
12.

Novel mutation of the KRT 10 gene in a Japanese patient with epidermolytic hyperkeratosis.

Makino T, Furuichi M, Asano Y, Shimizu T.

J Dermatol. 2012 Jan;39(1):87-9. doi: 10.1111/j.1346-8138.2011.01234.x. Epub 2011 Apr 5. No abstract available.

PMID:
21463361
13.

Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads.

Chiu HC, Jee SH, Sheen YS, Chu CY, Lin PJ, Liaw SH.

J Dermatol Sci. 2007 Jan;45(1):63-5. Epub 2006 Oct 30. No abstract available.

PMID:
17074468
14.

Asymptomatic leucoplakia of the prepuce.

Velázquez D, Casado I, de la Cueva P, Hernanz JM.

Clin Exp Dermatol. 2013 Jul;38(5):562-3. doi: 10.1111/j.1365-2230.2012.04429.x. No abstract available.

PMID:
23777501
15.

Duplication mutation of keratin 9 gene in a large Chinese family with epidermolytic palmoplantar keratoderma.

Zeng YP, Chai WX, Fang K, Wang BX, Zuo YG.

Eur J Dermatol. 2011 Mar-Apr;21(2):268-9. doi: 10.1684/ejd.2010.1244. No abstract available.

PMID:
21489919
16.

Missense mutation of keratin 9 (c.487C>T (p.R163W) in southern Chinese patients with epidermolytic palmoplantar keratoderma.

Xu CM, Chen XL, Chen CY, Zhang XN.

Eur J Dermatol. 2009 May-Jun;19(3):265-6. doi: 10.1684/ejd.2009.0631. Epub 2009 Feb 17. No abstract available.

PMID:
19223272
17.

Identification of the keratin 9 (KRT9) N161S mutation in a Chinese kindred with epidermolytic palmoplantar keratoderma.

Feng W, Han W, Man X, Jiang M, Bian C, Wang G, Li X, Yi D, Li J.

Eur J Dermatol. 2008 Jul-Aug;18(4):387-90. doi: 10.1684/ejd.2008.0432. Epub 2008 Jun 23.

PMID:
18573708
18.

A recurrent p.M157R mutation of keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma and literature review.

Liang YH, Liu QX, Huang L, Zeng K.

Int J Dermatol. 2014 Aug;53(8):e375-9. doi: 10.1111/ijd.12352. Epub 2014 Jun 5. Review. No abstract available.

PMID:
24899405
19.

Ichthyosis cribriformis: A new entity?

Larangeira de Almeida H Jr, Happle R, Blume-Peytavi U, de Castro LA.

J Am Acad Dermatol. 2008 Mar;58(3):505-7. doi: 10.1016/j.jaad.2007.03.034.

PMID:
18280353
20.

Epidermolytic hyperkeratosis with palmoplantar keratoderma in a patient with KRT10 mutation.

Morais P, Mota A, Baudrier T, Lopes JM, Cerqueira R, Tavares P, Azevedo F.

Eur J Dermatol. 2009 Jul-Aug;19(4):333-6. doi: 10.1684/ejd.2009.0684. Epub 2009 May 14.

PMID:
19443303

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