186 related articles for article (PubMed ID: 22031649)
1. Nevoid basal cell carcinoma syndrome.
Leger M; Quintana A; Tzu J; Yee H; Kamino H; Sanchez M
Dermatol Online J; 2011 Oct; 17(10):23. PubMed ID: 22031649
[TBL] [Abstract][Full Text] [Related]
2. Unusual cystic scalp lesions in Gorlin syndrome: a brief report.
Findley AB; Pride H
Pediatr Dermatol; 2010; 27(2):204-7. PubMed ID: 20537080
[TBL] [Abstract][Full Text] [Related]
3. Complications of the nevoid basal cell carcinoma syndrome: a case report.
Walter AW; Pivnick EK; Bale AE; Kun LE
J Pediatr Hematol Oncol; 1997; 19(3):258-62. PubMed ID: 9201152
[TBL] [Abstract][Full Text] [Related]
4. Medulloblastoma in the nevoid basal-cell carcinoma syndrome: case reports and review of the literature.
Lacombe D; Chateil JF; Fontan D; Battin J
Genet Couns; 1990; 1(3-4):273-7. PubMed ID: 2098052
[TBL] [Abstract][Full Text] [Related]
5. Two male patients with nevoid basal cell carcinoma syndrome from Turkey.
Tümer C; Er N; Balci S; Ataç A
Turk J Pediatr; 2001; 43(4):351-5. PubMed ID: 11765170
[TBL] [Abstract][Full Text] [Related]
6. [Basal cell nevus syndrome. Presentation of 2 cases. 1 associated with medulloblastoma].
Balsa RE; Ingratta SM; Galeano FA; Raffaeli CA; Drut R; Vestfrid M
Med Cutan Ibero Lat Am; 1985; 13(1):5-11. PubMed ID: 3887060
[TBL] [Abstract][Full Text] [Related]
7. Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.
Gloude NJ; Yoon JM; Crawford JR
Pediatr Blood Cancer; 2016 Jun; 63(6):1128-9. PubMed ID: 26840755
[No Abstract] [Full Text] [Related]
8. Nevoid basal cell carcinoma syndrome and non-Hodgkin's lymphoma.
Schulz-Butulis BA; Gilson R; Farley M; Keeling JH
Cutis; 2000 Jul; 66(1):35-8. PubMed ID: 10916689
[TBL] [Abstract][Full Text] [Related]
9. Gorlin-Goltz syndrome.
Ljubenović M; Ljubenović D; Binić I; Jovanović D; Stanojević M
Acta Dermatovenerol Alp Pannonica Adriat; 2007 Dec; 16(4):166-9. PubMed ID: 18204747
[TBL] [Abstract][Full Text] [Related]
10. Naevoid basal cell carcinoma syndrome in a 22-month-old child presenting with multiple basal cell carcinomas and a fetal rhabdomyoma.
Diociaiuti A; Inserra A; De Vega IF; Rota C; Surrenti T; Giraldi L; Piemontese MR; Giovannoni I; Callea F; El Hachem M
Acta Derm Venereol; 2015 Feb; 95(2):243-4. PubMed ID: 24816767
[No Abstract] [Full Text] [Related]
11. Basal cell nevus syndrome and medulloblastoma: a case report.
Romero Pérez JA; Lleras Santana I
Bol Asoc Med P R; 1993; 85(1-3):24-6. PubMed ID: 8060441
[TBL] [Abstract][Full Text] [Related]
12. Multifocal desmoplastic medulloblastoma in an african-american child with nevoid basal cell carcinoma (gorlin) syndrome. Case report.
Smucker PS; Smith JL
J Neurosurg; 2006 Oct; 105(4 Suppl):315-20. PubMed ID: 17328283
[TBL] [Abstract][Full Text] [Related]
13. Palmar pits associated with the nevoid basal cell carcinoma syndrome.
North JP; McCalmont TH; LeBoit P
J Cutan Pathol; 2012 Aug; 39(8):735-8. PubMed ID: 22845656
[No Abstract] [Full Text] [Related]
14. 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. PubMed ID: 18417377
[TBL] [Abstract][Full Text] [Related]
15. A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.
Durmaz CD; Evans G; Smith MJ; Ertop P; Akay BN; Tuncalı T
Cytogenet Genome Res; 2018; 154(2):57-61. PubMed ID: 29544218
[TBL] [Abstract][Full Text] [Related]
16. Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation.
Ragge NK; Salt A; Collin JR; Michalski A; Farndon PA
Br J Ophthalmol; 2005 Aug; 89(8):988-91. PubMed ID: 16024850
[TBL] [Abstract][Full Text] [Related]
17. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome.
Nakamura M; Tokura Y
Eur J Dermatol; 2009; 19(3):262-3. PubMed ID: 19213655
[No Abstract] [Full Text] [Related]
18. Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.
Škodrić-Trifunović V; Stjepanović M; Savić Ž; Ilić M; Kavečan I; Jovanović Privrodski J; Spasovski V; Stojiljković M; Pavlović S
Croat Med J; 2015 Feb; 56(1):63-7. PubMed ID: 25727044
[TBL] [Abstract][Full Text] [Related]
19. 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. PubMed ID: 20659694
[TBL] [Abstract][Full Text] [Related]
20. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]