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Items: 1 to 20 of 131

1.

[The Clark-Howel-Evans-McConnell syndrome. Observations in one family over 5 generations].

Simon M, Hagedorn M.

Hautarzt. 1997 Nov;48(11):800-5. Review. German.

PMID:
9518240
2.

Tylosis associated with carcinoma of the oesophagus and oral leukoplakia in a large Liverpool family--a review of six generations.

Ellis A, Field JK, Field EA, Friedmann PS, Fryer A, Howard P, Leigh IM, Risk J, Shaw JM, Whittaker J.

Eur J Cancer B Oral Oncol. 1994;30B(2):102-12. No abstract available.

PMID:
8032299
3.

Howel-Evans syndrome: a variant of ectodermal dysplasia.

Sroa N, Witman P.

Cutis. 2010 Apr;85(4):183-5.

PMID:
20486456
4.

[Focal palmoplantar and oral mucosa hyperkeratosis syndrome].

Bethke G, Kolde G, Bethke G, Reichart PA.

Mund Kiefer Gesichtschir. 2001 May;5(3):202-5. German.

PMID:
11432338
5.

Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.

Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Spurr NK, Weissenbach J, Marger D, Marger RS, Leigh IM.

Arch Dermatol. 1996 Jun;132(6):640-51. Review.

PMID:
8651714
6.

Genetic tylosis with malignancy: a study of a South Indian pedigree.

Yesudian P, Premalatha S, Thambiah AS.

Br J Dermatol. 1980 May;102(5):597-600.

PMID:
6446315
7.
8.

Oral leukoplakia associated with tylosis and esophageal carcinoma.

Tyldesley WR.

J Oral Pathol. 1974;3(2):62-70. No abstract available.

PMID:
4213563
9.

[Hereditary tylosis syndrome and esophagus cancer].

de Souza CA, Santos Ada C, Santos Lda C, Carneiro AL.

An Bras Dermatol. 2009 Sep-Oct;84(5):527-9. Portuguese.

10.

The gene for diffuse palmoplantar keratoderma of the type found in northern Sweden is localized to chromosome 12q11-q13.

Lind L, Lundström A, Hofer PA, Holmgren G.

Hum Mol Genet. 1994 Oct;3(10):1789-93.

PMID:
7531539
11.

Tylosis A with squamous cell carcinoma of the oesophagus in a Spanish family.

Varela AB, Blanco Rodríguez MM, Boullosa PE, Silva JG.

Eur J Gastroenterol Hepatol. 2011 Mar;23(3):286-8. doi: 10.1097/MEG.0b013e328344042d.

PMID:
21285883
12.

Acantholytic ectodermal dysplasia: clinicopathological study of a new desmosomal disorder.

Winik BC, Asial RA, McGrath JA, South AP, Boente MC.

Br J Dermatol. 2009 Apr;160(4):868-74. doi: 10.1111/j.1365-2133.2008.08946.x. Epub 2008 Nov 25.

PMID:
19067702
13.

Oral findings of Clouston's syndrome (hidrotic ectodermal dysplasia).

George DI Jr, Escobar VH.

Oral Surg Oral Med Oral Pathol. 1984 Mar;57(3):258-62. No abstract available.

PMID:
6584816
14.

[Clarke-Howel Evans' syndrome].

De Dulanto F, Camacho Martínez F, Armijo Moreno M, Naranjo Sintes R, Roldán González RM, Dulanto MC, Montero García M, Fernández Lloret S.

Actas Dermosifiliogr. 1977 Mar-Apr;68(3-4):127-38. Spanish. No abstract available.

PMID:
141196
15.

[Pachyonychia congenita. Keratin gene mutations with pleiotropic effect].

Swensson O.

Hautarzt. 1999 Jul;50(7):483-90. Review. German.

PMID:
10464680
16.

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).

Kelsell DP, Risk JM, Leigh IM, Stevens HP, Ellis A, Hennies HC, Reis A, Weissenbach J, Bishop DT, Spurr NK, Field JK.

Hum Mol Genet. 1996 Jun;5(6):857-60.

PMID:
8776604
17.

RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome.

Blaydon DC, Etheridge SL, Risk JM, Hennies HC, Gay LJ, Carroll R, Plagnol V, McRonald FE, Stevens HP, Spurr NK, Bishop DT, Ellis A, Jankowski J, Field JK, Leigh IM, South AP, Kelsell DP.

Am J Hum Genet. 2012 Feb 10;90(2):340-6. doi: 10.1016/j.ajhg.2011.12.008. Epub 2012 Jan 19.

18.

Connexin disorders of the skin.

Richard G.

Adv Dermatol. 2001;17:243-77. Review. No abstract available.

PMID:
11758118
19.

[The p16 methylation in oral leukoplakia and oral squamous cell carcinoma].

Liu HW, Hu BQ, Cao CF.

Zhonghua Kou Qiang Yi Xue Za Zhi. 2005 Mar;40(2):94-7. Chinese.

PMID:
15842853
20.

Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer.

Iwaya T, Maesawa C, Ogasawara S, Tamura G.

Gastroenterology. 1998 Jun;114(6):1206-10.

PMID:
9609757

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