195 related articles for article (PubMed ID: 33063358)
1. Retrospective analysis of the histopathologic features of basal cell carcinomas in pediatric patients with basal cell nevus syndrome.
Nguyen CV; Rubin AI; Smith A; Castelo-Soccio L
J Cutan Pathol; 2021 Mar; 48(3):390-395. PubMed ID: 33063358
[TBL] [Abstract][Full Text] [Related]
2. Features of basal cell carcinomas in basal cell nevus syndrome.
Tom WL; Hurley MY; Oliver DS; Shah MR; Bree AF
Am J Med Genet A; 2011 Sep; 155A(9):2098-104. PubMed ID: 21834051
[TBL] [Abstract][Full Text] [Related]
3. Genetic profiling of basal cell carcinomas detects postzygotic mosaicism in basal cell naevus syndrome.
Reinders MGHC; Cosgun B; Gijezen LMC; van Oosterhoud CN; Kelleners-Smeets NWJ; Vermander E; Vreeburg M; Steijlen PM; Mosterd K; van Geel M
Br J Dermatol; 2019 Sep; 181(3):587-591. PubMed ID: 30520020
[TBL] [Abstract][Full Text] [Related]
4. SUFU-associated Gorlin syndrome: Expanding the spectrum between classic nevoid basal cell carcinoma syndrome and multiple hereditary infundibulocystic basal cell carcinoma.
Álvarez-Salafranca M; García-García M; Montes-Torres A; Rivera-Fuertes I; López-Giménez MT; Ara M
Australas J Dermatol; 2023 May; 64(2):249-254. PubMed ID: 36825822
[TBL] [Abstract][Full Text] [Related]
5. Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome.
Kaibuchi-Ando K; Takeichi T; Ito Y; Takeuchi S; Yamashita Y; Yamada M; Muro Y; Ogi T; Akiyama M
Nagoya J Med Sci; 2021 May; 83(2):393-396. PubMed ID: 34239189
[TBL] [Abstract][Full Text] [Related]
6. Basal cell nevus syndrome: clinical and molecular review and case report.
Pino LC; Balassiano LK; Sessim M; de Almeida AP; Empinotti VD; Semenovitch I; Treu C; Lupi O
Int J Dermatol; 2016 Apr; 55(4):367-75. PubMed ID: 26356331
[TBL] [Abstract][Full Text] [Related]
7. Basaloid follicular hamartomas in pediatric Basal Cell Nevus Syndrome: A diagnostic challenge.
Besagni F; Dika E; Ricci C; Misciali C; Veronesi G; Corti B; Gurioli C; Neri I
J Dermatol; 2021 Jul; 48(7):1101-1105. PubMed ID: 34021633
[TBL] [Abstract][Full Text] [Related]
8. Genomic Stability in Syndromic Basal Cell Carcinoma.
Chiang A; Jaju PD; Batra P; Rezaee M; Epstein EH; Tang JY; Sarin KY
J Invest Dermatol; 2018 May; 138(5):1044-1051. PubMed ID: 29111235
[TBL] [Abstract][Full Text] [Related]
9. PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome.
Gielen RCAM; Reinders MGHC; Koillinen HK; Paulussen ADC; Mosterd K; van Geel M
J Hum Genet; 2018 Sep; 63(9):965-969. PubMed ID: 29930296
[TBL] [Abstract][Full Text] [Related]
10. Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
Huq AJ; Walsh M; Rajagopalan B; Finlay M; Trainer AH; Bonnet F; Sevenet N; Winship IM
Fam Cancer; 2018 Oct; 17(4):601-606. PubMed ID: 29356994
[TBL] [Abstract][Full Text] [Related]
11. Expression of the Sonic Hedgehog receptor "PATCHED" in basal cell carcinomas and odontogenic keratocysts.
Zedan W; Robinson PA; Markham AF; High AS
J Pathol; 2001 Aug; 194(4):473-7. PubMed ID: 11523056
[TBL] [Abstract][Full Text] [Related]
12. A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome.
Ozcan G; Balta B; Sekerci AE; Etoz OA; Martinuzzi C; Kara O; Pastorino L; Kocoglu F; Ulker O; Erdogan M
Indian J Pathol Microbiol; 2016; 59(3):335-8. PubMed ID: 27510672
[TBL] [Abstract][Full Text] [Related]
13. New mutations and an updated database for the patched-1 (PTCH1) gene.
Reinders MG; van Hout AF; Cosgun B; Paulussen AD; Leter EM; Steijlen PM; Mosterd K; van Geel M; Gille JJ
Mol Genet Genomic Med; 2018 May; 6(3):409-415. PubMed ID: 29575684
[TBL] [Abstract][Full Text] [Related]
14. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.
Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L
J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428
[TBL] [Abstract][Full Text] [Related]
15. Gorlin syndrome or basal cell nevus syndrome (BCNS): A case report.
Shivaswamy KN; Sumathy TK; Shyamprasad AL; Ranganathan C
Dermatol Online J; 2010 Sep; 16(9):6. PubMed ID: 20875327
[TBL] [Abstract][Full Text] [Related]
16. Infundibulocystic basal cell carcinoma of the eyelid in basal cell nevus syndrome.
Belliveau MJ; Coupal DJ; Brownstein S; Jordan DR; Prokopetz R
Ophthalmic Plast Reconstr Surg; 2010; 26(3):147-52. PubMed ID: 20489535
[TBL] [Abstract][Full Text] [Related]
17. Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome.
Requena L; Fariña MC; Robledo M; Sangueza OP; Sanchez E; Villanueva A; Marquina A; Tamarit R
Arch Dermatol; 1999 Oct; 135(10):1227-35. PubMed ID: 10522671
[TBL] [Abstract][Full Text] [Related]
18. "PTCH"-ing it together: a basal cell nevus syndrome review.
Lam C; Ou JC; Billingsley EM
Dermatol Surg; 2013 Nov; 39(11):1557-72. PubMed ID: 23725561
[TBL] [Abstract][Full Text] [Related]
19. Unexpected phenotype in a frameshift mutation of PTCH1.
Beltrami B; Prada E; Tolva G; Scuvera G; Silipigni R; Graziani D; Bulfamante G; Gervasini C; Marchisio P; Milani D
Mol Genet Genomic Med; 2020 Jan; 8(1):e987. PubMed ID: 31578813
[TBL] [Abstract][Full Text] [Related]
20. PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.
Santos DC; Zaphiropoulos PG; Neto CF; Pimentel ER; Sanches JA; Ruiz IR
Int J Dermatol; 2011 Jul; 50(7):838-43. PubMed ID: 21699520
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
