Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 114

1.

Genetic skin diseases predisposing to basal cell carcinoma.

Castori M, Morrone A, Kanitakis J, Grammatico P.

Eur J Dermatol. 2012 May-Jun;22(3):299-309. doi: 10.1684/ejd.2011.1633. Review.

PMID:
22391625
2.

Clinical and dermatoscopic findings in Bazex-Dupré-Christol and Gorlin-Goltz syndromes.

Tiodorovic-Zivkovic D, Zalaudek I, Ferrara G, Giorgio CM, Di Nola K, Procaccini EM, Argenziano G.

J Am Acad Dermatol. 2010 Oct;63(4):722-4. doi: 10.1016/j.jaad.2009.06.026. No abstract available.

PMID:
20846576
3.

Linkage refinement of Bazex-Dupré-Christol syndrome to an 11·4-Mb interval on chromosome Xq25-27.1.

Parren LJ, Abuzahra F, Wagenvoort T, Koene F, Van Steensel MA, Steijlen PM, Van Geel M, Frank J.

Br J Dermatol. 2011 Jul;165(1):201-3. doi: 10.1111/j.1365-2133.2011.10219.x. No abstract available.

PMID:
21219295
4.

Hereditary tumour syndromes featuring basal cell carcinomas.

Parren LJ, Frank J.

Br J Dermatol. 2011 Jul;165(1):30-4. doi: 10.1111/j.1365-2133.2011.10334.x. Epub 2011 Jun 3. Review.

PMID:
21428980
5.

Familial syndromes with skin tumor markers.

Hauck RM, Manders EK.

Ann Plast Surg. 1994 Jul;33(1):102-11. Review.

PMID:
7944188
6.

Bazex-Dupré-Christol syndrome: an ectodermal dysplasia with skin appendage neoplasms.

Castori M, Castiglia D, Passarelli F, Paradisi M.

Eur J Med Genet. 2009 Jul-Aug;52(4):250-5. doi: 10.1016/j.ejmg.2008.12.003. Epub 2008 Dec 25.

PMID:
19138767
7.

Bazex-Dupré-Christol syndrome in a 1-year-old boy and his mother.

Barcelos AC, Nico MM.

Pediatr Dermatol. 2008 Jan-Feb;25(1):112-3. doi: 10.1111/j.1525-1470.2007.00596.x.

PMID:
18304168
8.

Familial skin cancer syndromes: Increased risk of nonmelanotic skin cancers and extracutaneous tumors.

Jaju PD, Ransohoff KJ, Tang JY, Sarin KY.

J Am Acad Dermatol. 2016 Mar;74(3):437-51; quiz 452-4. doi: 10.1016/j.jaad.2015.08.073. Review.

PMID:
26892653
9.

[Diffuse milia in an infant indicative of Bazex-Dupré-Christol syndrome].

Gréco M, Bessaguet-Küpfer I, Bourrigan M, Plantin P.

Ann Dermatol Venereol. 2006 Aug-Sep;133(8-9 Pt 1):697-9. French.

PMID:
17053742
10.

Genetics of skin appendage neoplasms and related syndromes.

Lee DA, Grossman ME, Schneiderman P, Celebi JT.

J Med Genet. 2005 Nov;42(11):811-9. Review.

12.

[Bazex-Dupré-Christol syndrome. Follicular atrophoderma, multiple basal cell carcinomas and hypotrichosis].

Herges A, Stieler W, Stadler R.

Hautarzt. 1993 Jun;44(6):385-91. Review. German.

PMID:
8335462
13.

Sporadic Bazex-Dupré-Christol-like syndrome: early onset basal cell carcinoma, hypohidrosis, hypotrichosis, and prominent milia.

Glaessl A, Hohenlautner U, Landthaler M, Vogt T.

Dermatol Surg. 2000 Feb;26(2):152-4. Review.

PMID:
10691946
14.

Developmental genes and cancer: role of patched in basal cell carcinoma of the skin.

Gailani MR, Bale AE.

J Natl Cancer Inst. 1997 Aug 6;89(15):1103-9. Review.

PMID:
9262247
15.

The gene for Bazex-Dupré-Christol syndrome maps to chromosome Xq.

Vabres P, Lacombe D, Rabinowitz LG, Aubert G, Anderson CE, Taieb A, Bonafé JL, Hors-Cayla MC.

J Invest Dermatol. 1995 Jul;105(1):87-91.

16.

Dermoscopy for the pediatric dermatologist, part ii: dermoscopy of genetic syndromes with cutaneous manifestations and pediatric vascular lesions.

Haliasos EC, Kerner M, Jaimes N, Zalaudek I, Malvehy J, Lanschuetzer CM, Hinter H, Hofmann-Wellenhof R, Braun RP, Marghoob AA.

Pediatr Dermatol. 2013 Mar-Apr;30(2):172-81. doi: 10.1111/j.1525-1470.2012.01874.x. Epub 2012 Sep 20. Review.

PMID:
22994304
17.

Cancer-associated genodermatoses: a personal history.

Burgdorf WH.

Exp Dermatol. 2006 Sep;15(9):653-66. Review.

PMID:
16881962
18.

Brooke-Spiegler syndrome: report of a case with a novel mutation in the CYLD gene and different types of somatic mutations in benign and malignant tumors.

Kazakov DV, Schaller J, Vanecek T, Kacerovska D, Michal M.

J Cutan Pathol. 2010 Aug;37(8):886-90. doi: 10.1111/j.1600-0560.2010.01511.x. Epub 2010 Feb 4.

PMID:
20132422
19.

Understanding photodermatoses associated with defective DNA repair: Syndromes with cancer predisposition.

Giordano CN, Yew YW, Spivak G, Lim HW.

J Am Acad Dermatol. 2016 Nov;75(5):855-870. doi: 10.1016/j.jaad.2016.03.045. Review.

PMID:
27745641
20.

Specific UV-induced mutation spectrum in the p53 gene of skin tumors from DNA-repair-deficient xeroderma pigmentosum patients.

Dumaz N, Drougard C, Sarasin A, Daya-Grosjean L.

Proc Natl Acad Sci U S A. 1993 Nov 15;90(22):10529-33.

Supplemental Content

Support Center