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Items: 1 to 20 of 147

1.

Conjunctival ganglioglioma as a feature of basal cell nevus syndrome.

Sauer A, Blavin J, Lhermitte B, Speeg-Schatz C.

J AAPOS. 2011 Aug;15(4):387-8. doi: 10.1016/j.jaapos.2011.05.010.

PMID:
21907124
2.

Gorlin syndrome or basal cell nevus syndrome (BCNS): A case report.

Shivaswamy KN, Sumathy TK, Shyamprasad AL, Ranganathan C.

Dermatol Online J. 2010 Sep 15;16(9):6.

3.

Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Lo Muzio L.

Orphanet J Rare Dis. 2008 Nov 25;3:32. doi: 10.1186/1750-1172-3-32. Review.

4.

Gorlin syndrome associated with basal cell carcinoma of the vulva: A case report.

Giuliani M, Di Stefano L, Zoccali G, Angelone E, Leocata P, Mascaretti G.

Eur J Gynaecol Oncol. 2006;27(5):519-22.

PMID:
17139991
5.

Odontogenic keratocyst and uterus bicornis in nevoid basal cell carcinoma syndrome: case report and literature review.

Ramaglia L, Morgese F, Pighetti M, Saviano R.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Aug;102(2):217-9. Epub 2006 Jan 19. Review.

PMID:
16876065
6.

[Gorlin-Goltz syndrome: review of the neuroradiological and maxillofacial features illustrated with two clinical cases].

Safronova MM, Arantes M, Lima I, Domingues S, Almeida M, Moniz P.

Acta Med Port. 2010 Nov-Dec;23(6):1119-26. Epub 2010 Dec 28. Portuguese.

7.

Nevoid basal cell carcinoma syndrome: a review of the literature.

Manfredi M, Vescovi P, Bonanini M, Porter S.

Int J Oral Maxillofac Surg. 2004 Mar;33(2):117-24. Review.

PMID:
15050066
8.

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S, Goldstein A, Dean M, Bale AE.

Am J Hum Genet. 1996 Aug;59(2):417-22.

9.

Ameloblastoma associated with the nevoid basal cell carcinoma (Gorlin) syndrome.

Eslami B, Lorente C, Kieff D, Caruso PA, Faquin WC.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008 Jun;105(6):e10-3. doi: 10.1016/j.tripleo.2008.01.034. Epub 2008 Apr 16.

PMID:
18417377
10.

[The Gorlin syndrome. A review of 11 cases].

Alegre M, Puig L, de Moragas JM.

Rev Clin Esp. 1995 Oct;195(10):684-7. Review. Spanish.

PMID:
8532924
11.

Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome.

Ponti G, Pollio A, Mignogna MD, Pellacani G, Pastorino L, Bianchi-Scarrà G, Di Gregorio C, Magnoni C, Azzoni P, Greco M, Seidenari S.

Cancer Genet. 2012 Apr;205(4):177-81. doi: 10.1016/j.cancergen.2012.01.012.

PMID:
22559979
12.

Gorlin syndrome: a case report.

Patil K, Mahima VG, Gupta B.

J Indian Soc Pedod Prev Dent. 2005 Oct-Dec;23(4):198-203. Review.

13.

Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report.

Sasaki R, Miyashita T, Matsumoto N, Fujii K, Saito K, Ando T.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2010 Aug;110(2):e41-6. doi: 10.1016/j.tripleo.2010.04.006.

PMID:
20659694
14.

Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis.

Pan S, Dong Q, Sun LS, Li TJ.

Clin Cancer Res. 2010 Jan 15;16(2):442-50. doi: 10.1158/1078-0432.CCR-09-2574. Epub 2010 Jan 12.

15.

Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.

Rodrigues AL, Carvalho A, Cabral R, Carneiro V, Gilardi P, Duarte CP, Puente-Prieto J, Santos P, Mota-Vieira L.

Genet Mol Res. 2014 Jul 25;13(3):5654-63. doi: 10.4238/2014.July.25.21.

16.

[From gene to disease: basal cell naevus syndrome].

de Meij TG, Baars MJ, Gille JJ, Hack WW, Haasnoot K, van Hagen JM.

Ned Tijdschr Geneeskd. 2005 Jan 8;149(2):78-81. Review. Dutch.

PMID:
15688838
17.

Nevoid basal cell carcinoma syndrome.

Karthiga KS, Sivapatha Sundharam B, Manikandan R.

Indian J Dent Res. 2006 Jan-Mar;17(1):50-3.

18.

[Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years].

Rupprecht M, Mensing CH, Barvencik F, Ittrich H, Heiland M, Rueger JM, Amling M, Pogoda P.

Rofo. 2007 Jun;179(6):618-26. Epub 2007 May 9. Review. German.

PMID:
17492539
19.

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.

Boonen SE, Stahl D, Kreiborg S, Rosenberg T, Kalscheuer V, Larsen LA, Tommerup N, Brøndum-Nielsen K, Tümer Z.

Am J Med Genet A. 2005 Jan 30;132A(3):324-8. Review.

PMID:
15690381
20.

Familial multiple odontogenic keratocysts.

Wang XX, Zhang J, Wei FC.

J Dent Child (Chic). 2007 May-Aug;74(2):140-2. Review.

PMID:
18477436
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