Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 96

1.

[Hereditary head and neck tumors].

Schwarz-Furlan S, Brase C, Stockmann P, Furlan I, Hartmann A.

Pathologe. 2010 Oct;31(6):477-84. doi: 10.1007/s00292-010-1359-1. German.

PMID:
20844882
2.

Generation and molecular characterization of head and neck squamous cell lines of fanconi anemia patients.

van Zeeburg HJ, Snijders PJ, Pals G, Hermsen MA, Rooimans MA, Bagby G, Soulier J, Gluckman E, Wennerberg J, Leemans CR, Joenje H, Brakenhoff RH.

Cancer Res. 2005 Feb 15;65(4):1271-6.

3.

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.

Bayley JP, van Minderhout I, Weiss MM, Jansen JC, Oomen PH, Menko FH, Pasini B, Ferrando B, Wong N, Alpert LC, Williams R, Blair E, Devilee P, Taschner PE.

BMC Med Genet. 2006 Jan 11;7:1.

4.

Genomic instability in head and neck cancer patients.

Friedlander PL.

Head Neck. 2001 Aug;23(8):683-91. Review.

PMID:
11443752
5.

Defects in the Fanconi Anemia Pathway and Chromatid Cohesion in Head and Neck Cancer.

Stoepker C, Ameziane N, van der Lelij P, Kooi IE, Oostra AB, Rooimans MA, van Mil SE, Brink A, Dietrich R, Balk JA, Ylstra B, Joenje H, Feller SM, Brakenhoff RH.

Cancer Res. 2015 Sep 1;75(17):3543-53. doi: 10.1158/0008-5472.CAN-15-0528. Epub 2015 Jun 29.

PMID:
26122845
6.

Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome.

Honavar SG, Shields JA, Shields CL, Eagle RC Jr, Demirci H, Mahmood EZ.

Ophthalmology. 2001 Jun;108(6):1115-23.

PMID:
11382639
7.

Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.

Aszterbaum M, Rothman A, Johnson RL, Fisher M, Xie J, Bonifas JM, Zhang X, Scott MP, Epstein EH Jr.

J Invest Dermatol. 1998 Jun;110(6):885-8.

PMID:
9620294
8.

Molecular pathology of skin neoplasms of the head and neck.

Kraft S, Granter SR.

Arch Pathol Lab Med. 2014 Jun;138(6):759-87. doi: 10.5858/arpa.2013-0157-RA. Review.

PMID:
24878016
9.

The nevoid basal cell carcinoma syndrome. Histopathology of the basal cell tumors.

Lindeberg H, Jepsen FL.

J Cutan Pathol. 1983 Feb;10(1):68-72.

PMID:
6841732
10.

Squamous cell carcinomas of the head and neck in Fanconi anemia: risk, prevention, therapy, and the need for guidelines.

Scheckenbach K, Wagenmann M, Freund M, Schipper J, Hanenberg H.

Klin Padiatr. 2012 Apr;224(3):132-8. doi: 10.1055/s-0032-1308989. Epub 2012 Apr 13. Review.

11.

On the association of succinate dehydrogenase mutations with hereditary paraganglioma.

Baysal BE.

Trends Endocrinol Metab. 2003 Dec;14(10):453-9. Review.

PMID:
14643060
12.

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.

Benn DE, Croxson MS, Tucker K, Bambach CP, Richardson AL, Delbridge L, Pullan PT, Hammond J, Marsh DJ, Robinson BG.

Oncogene. 2003 Mar 6;22(9):1358-64.

PMID:
12618761
13.
14.

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P.

Genes Chromosomes Cancer. 2001 Jul;31(3):274-81.

PMID:
11391798
15.

Microsatellite instability in squamous cell carcinomas of the head and neck related to field cancerization phenomena.

Piccinin S, Gasparotto D, Vukosavljevic T, Barzan L, Sulfaro S, Maestro R, Boiocchi M.

Br J Cancer. 1998 Nov;78(9):1147-51.

16.

Detection of EGFR- and HER2-activating mutations in squamous cell carcinoma involving the head and neck.

Willmore-Payne C, Holden JA, Layfield LJ.

Mod Pathol. 2006 May;19(5):634-40.

17.

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas.

Baysal BE, Willett-Brozick JE, Lawrence EC, Drovdlic CM, Savul SA, McLeod DR, Yee HA, Brackmann DE, Slattery WH 3rd, Myers EN, Ferrell RE, Rubinstein WS.

J Med Genet. 2002 Mar;39(3):178-83.

18.

Downregulation of Fanconi anemia genes in sporadic head and neck squamous cell carcinoma.

Wreesmann VB, Estilo C, Eisele DW, Singh B, Wang SJ.

ORL J Otorhinolaryngol Relat Spec. 2007;69(4):218-25. Epub 2007 Apr 4.

PMID:
17409780
19.

Genetic and clinicopathologic aspects of Gorlin-Goltz syndrome (NBCCS): presentation of two case reports and literature review.

Acocella A, Sacco R, Bertolai R, Sacco N.

Minerva Stomatol. 2009 Jan-Feb;58(1-2):43-53. Review. English, Italian.

PMID:
19234436
20.

Genomic instabilities in squamous cell carcinoma of head and neck from the Indian population.

Chakrabarti S, Sengupta S, Sengupta A, Basak SN, Roy A, Panda C, Roychoudhury S.

Mol Carcinog. 2006 Apr;45(4):270-7.

PMID:
16402388
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk