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Items: 1 to 20 of 97

1.

KID syndrome: histopathological, immunohistochemical and molecular analysis of precancerous and cancerous skin lesions.

Bergman R, Mercer A, Indelman M, Sprecher E, Haim N, Zoller L, Ben-Izhak O, Hershkovitz D.

Br J Dermatol. 2012 Feb;166(2):455-7. doi: 10.1111/j.1365-2133.2011.10577.x. Epub 2011 Nov 17. No abstract available.

PMID:
21848689
2.

Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas.

Grob JJ, Breton A, Bonafe JL, Sauvan-Ferdani M, Bonerandi JJ.

Arch Dermatol. 1987 Jun;123(6):777-82.

PMID:
3579358
3.

A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation.

Arndt S, Aschendorff A, Schild C, Beck R, Maier W, Laszig R, Birkenhäger R.

Otol Neurotol. 2010 Feb;31(2):210-5. doi: 10.1097/MAO.0b013e3181cc09cd.

PMID:
20101161
4.

Extending the phenotypic spectrum of keratitis-ichthyosis-deafness syndrome: report of a patient with GJB2 (G12R) Connexin 26 mutation and unusual clinical findings.

Lazic T, Li Q, Frank M, Uitto J, Zhou LH.

Pediatr Dermatol. 2012 May-Jun;29(3):349-57. doi: 10.1111/j.1525-1470.2011.01425.x. Epub 2011 Oct 20.

PMID:
22011219
5.

Connexin 26 (GJB2) mutations in keratitis-ichthyosis-deafness syndrome presenting with squamous cell carcinoma.

Sakabe J, Yoshiki R, Sugita K, Haruyama S, Sawada Y, Kabashima R, Bito T, Nakamura M, Tokura Y.

J Dermatol. 2012 Sep;39(9):814-5. doi: 10.1111/j.1346-8138.2011.01414.x. Epub 2011 Nov 21. Review. No abstract available.

PMID:
22098592
6.

p53 immunohistochemical expression in early posttransplant-associated malignant and premalignant cutaneous lesions.

Ferrándiz C, Fuente MJ, Fernández-Figueras MT, Bielsa I, Just M.

Dermatol Surg. 1999 Feb;25(2):97-101.

PMID:
10037511
7.

HID and KID syndromes are associated with the same connexin 26 mutation.

van Geel M, van Steensel MA, Küster W, Hennies HC, Happle R, Steijlen PM, König A.

Br J Dermatol. 2002 Jun;146(6):938-42.

PMID:
12072059
8.

Squamous cell carcinoma arising from Keratitis-ichthyosis-deafness syndrome.

Mayama H, Fujimura T, Asano M, Kambayashi Y, Numata Y, Aiba S.

Acta Derm Venereol. 2013 Sep 4;93(5):583-4. doi: 10.2340/00015555-1535. No abstract available.

9.

KID versus KED: What's in a name.

Williams ML, McCalmont TH.

Pediatr Dermatol. 1996 Mar-Apr;13(2):154-7. No abstract available.

PMID:
9122077
10.

Squamous cell carcinoma in congenital ichthyosis with deafness and keratitis. A case report and review of the literature.

Madariaga J, Fromowitz F, Phillips M, Hoover HC Jr.

Cancer. 1986 May 15;57(10):2026-9.

11.

Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications.

Haruna K, Suga Y, Oizumi A, Mizuno Y, Endo H, Shimizu T, Hasegawa T, Ikeda S.

J Dermatol. 2010 Jul;37(7):680-2. doi: 10.1111/j.1346-8138.2010.00839.x. No abstract available.

PMID:
20629838
12.

Keratitis, ichthyosis, and deafness syndrome with development of multiple cutaneous neoplasms.

Hazen PG, Carney P, Lynch WS.

Int J Dermatol. 1989 Apr;28(3):190-1. No abstract available.

PMID:
2707945
13.

A trichilemmal carcinoma arising from a proliferating trichilemmal cyst: a response.

Monteagudo C.

Hum Pathol. 1999 Feb;30(2):247-8. No abstract available.

PMID:
10029459
15.

A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?

Lazic T, Horii KA, Richard G, Wasserman DI, Antaya RJ.

Pediatr Dermatol. 2008 Sep-Oct;25(5):535-40. doi: 10.1111/j.1525-1470.2008.00767.x.

PMID:
18950394
16.

p53 immunostaining and image cytometry DNA analysis in precancerous and cancerous squamous epithelial lesions of the larynx.

Munck-Wikland E, Kuylenstierna R, Lindholm J, Auer G.

Head Neck. 1997 Mar;19(2):107-15.

PMID:
9059867
17.

Mutations of connexin 26 (GJB2) gene in a Chinese keratitis-ichthyosis-deafness syndrome patient with squamous cell carcinoma.

Liu J, Fang S, Ding Q, Wang Y, Ye T, Zhu H, Zhang X, Li B, Xu Y, Li Z.

J Dermatol. 2016 Jan;43(1):104-6. doi: 10.1111/1346-8138.13145. Epub 2015 Oct 7. No abstract available.

PMID:
26444850
18.

A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.

van Steensel MA, van Geel M, Nahuys M, Smitt JH, Steijlen PM.

J Invest Dermatol. 2002 Apr;118(4):724-7.

19.

Keratitis, ichthyosis and deafness (KID)-syndrome: report of three cases and a review of the literature.

Langer K, Konrad K, Wolff K.

Br J Dermatol. 1990 May;122(5):689-97. Review.

PMID:
2191710
20.

Alterations in gene expression and activity during squamous cell carcinoma development.

Serewko MM, Popa C, Dahler AL, Smith L, Strutton GM, Coman W, Dicker AJ, Saunders NA.

Cancer Res. 2002 Jul 1;62(13):3759-65.

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