130 related articles for article (PubMed ID: 29757857)
1. BRCA1-Associated Protein-1 Tumor Predisposition Syndrome in a Patient With Numerous Basal Cell Carcinomas.
Ren V; Bloomquist L; Orengo I; Rosen T
Dermatol Surg; 2019 Feb; 45(2):316-318. PubMed ID: 29757857
[No Abstract] [Full Text] [Related]
2. Skin Cancer Associated Genodermatoses: A Literature Review.
Schierbeck J; Vestergaard T; Bygum A
Acta Derm Venereol; 2019 Apr; 99(4):360-369. PubMed ID: 30653245
[TBL] [Abstract][Full Text] [Related]
3. A novel CYLD gene mutation and multiple basal cell carcinomas in a patient with Brooke-Spiegler syndrome.
Shiver M; Hughes M; Naylor M; McLarney B; Stolle C; Shalin S; Gao L
Clin Exp Dermatol; 2016 Jan; 41(1):98-100. PubMed ID: 25976026
[No Abstract] [Full Text] [Related]
4. Hereditary melanoma.
Bonadies DC; Bale AE
Curr Probl Cancer; 2011; 35(4):162-72. PubMed ID: 21911180
[No Abstract] [Full Text] [Related]
5. Basal cell carcinoma arising in association with trichoepithelioma in a case of Brooke-Spiegler syndrome with a novel genetic mutation in CYLD.
Melly L; Lawton G; Rajan N
J Cutan Pathol; 2012 Oct; 39(10):977-8. PubMed ID: 22882113
[No Abstract] [Full Text] [Related]
6. The genetics of melanoma: the UK experience.
Newton Bishop JA; Harland M; Bishop DT
Clin Exp Dermatol; 1998 Jul; 23(4):158-61. PubMed ID: 9894359
[TBL] [Abstract][Full Text] [Related]
7. Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in Norway.
Levin T; Mæhle L
Fam Cancer; 2017 Apr; 16(2):257-265. PubMed ID: 27804060
[TBL] [Abstract][Full Text] [Related]
8. Severely disfiguring multiple familial trichoepitheliomas with basal cell carcinoma.
Mapar MA; Ranjbari N; Afshar N; Karimzadeh I; Karimzadeh A
Indian J Dermatol Venereol Leprol; 2014; 80(4):349-52. PubMed ID: 25035368
[No Abstract] [Full Text] [Related]
9. Genetic diseases associated with an increased risk of skin cancer development in childhood.
Fogel AL; Sarin KY; Teng JMC
Curr Opin Pediatr; 2017 Aug; 29(4):426-433. PubMed ID: 28525403
[TBL] [Abstract][Full Text] [Related]
10. Hereditary tumour syndromes featuring basal cell carcinomas.
Parren LJ; Frank J
Br J Dermatol; 2011 Jul; 165(1):30-4. PubMed ID: 21428980
[TBL] [Abstract][Full Text] [Related]
11. Diagnosis and Management of Hereditary Basal Cell Skin Cancer.
Shanley S; McCormack C
Recent Results Cancer Res; 2016; 205():191-212. PubMed ID: 27075355
[TBL] [Abstract][Full Text] [Related]
12. Compound lesion of a basal cell carcinoma and a malignant melanoma: is there a common genetic origin?
Sharma SJ; Kreisel M; Holler C; Kroll T; Gamerdinger U; Gattenloehner S; Klussmann JP; Wittekindt C
Eur Arch Otorhinolaryngol; 2015 Feb; 272(2):505-9. PubMed ID: 25297533
[No Abstract] [Full Text] [Related]
13. [MITF: a genetic key to melanoma and renal cell carcinoma?].
Bertolotto C; Lesueur F; Bressac de Paillerets B
Med Sci (Paris); 2012 Mar; 28(3):258-61. PubMed ID: 22480646
[No Abstract] [Full Text] [Related]
14. Update on familial cancer syndromes and the skin.
Tsao H
J Am Acad Dermatol; 2000 Jun; 42(6):939-69; quiz 970-2. PubMed ID: 10827397
[TBL] [Abstract][Full Text] [Related]
15. Management of familial melanoma and nonmelanoma skin cancer syndromes.
Santillan AA; Cherpelis BS; Glass LF; Sondak VK
Surg Oncol Clin N Am; 2009 Jan; 18(1):73-98, viii. PubMed ID: 19056043
[TBL] [Abstract][Full Text] [Related]
16. Nevoid basal cell carcinoma syndrome or multiple hereditary infundibulocystic basal cell carcinoma syndrome?
Crawford KM; Kobayashi T
J Am Acad Dermatol; 2004 Dec; 51(6):989-95. PubMed ID: 15583598
[TBL] [Abstract][Full Text] [Related]
17. Basal cell carcinomas, coarse sparse hair, and milia.
Oley CA; Sharpe H; Chenevix-Trench G
Am J Med Genet; 1992 Jul; 43(5):799-804. PubMed ID: 1642265
[No Abstract] [Full Text] [Related]
18. Germline CDKN2A mutations in childhood melanoma: a case of melanoma-pancreatic cancer syndrome.
Gironi LC; Colombo E; Farinelli P; Giorgione R; Bozzola C; Ogliara P; Pasini B
Int J Dermatol; 2015 Dec; 54(12):e553-5. PubMed ID: 26381259
[No Abstract] [Full Text] [Related]
19. A familial syndromic association between cutaneous malignant melanoma and neural system tumours.
Scope A; Friedman E; Azizi E
Br J Dermatol; 2004 Dec; 151(6):1278-9; author reply 1279. PubMed ID: 15606533
[No Abstract] [Full Text] [Related]
20. Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
Whelan AJ; Bartsch D; Goodfellow PJ
N Engl J Med; 1995 Oct; 333(15):975-7. PubMed ID: 7666917
[No Abstract] [Full Text] [Related]
[Next] [New Search]