163 related articles for article (PubMed ID: 17328283)
1. 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]
2. Nevoid basal cell carcinoma syndrome: relation with desmoplastic medulloblastoma in infancy. A population-based study and review of the literature.
Amlashi SF; Riffaud L; Brassier G; Morandi X
Cancer; 2003 Aug; 98(3):618-24. PubMed ID: 12879481
[TBL] [Abstract][Full Text] [Related]
3. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
Vortmeyer AO; Stavrou T; Selby D; Li G; Weil RJ; Park WS; Moon YW; Chandra R; Goldstein AM; Zhuang Z
Cancer; 1999 Jun; 85(12):2662-7. PubMed ID: 10375116
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients.
Chidambaram A; Goldstein AM; Gailani MR; Gerrard B; Bale SJ; DiGiovanna JJ; Bale AE; Dean M
Cancer Res; 1996 Oct; 56(20):4599-601. PubMed ID: 8840969
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
Unden AB; Holmberg E; Lundh-Rozell B; Stähle-Bäckdahl M; Zaphiropoulos PG; Toftgård R; Vorechovsky I
Cancer Res; 1996 Oct; 56(20):4562-5. PubMed ID: 8840960
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction.
Korczak JF; Brahim JS; DiGiovanna JJ; Kase RG; Wexler LH; Goldstein AM
Am J Med Genet; 1997 Mar; 69(3):309-14. PubMed ID: 9096762
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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; 13(3):5654-63. PubMed ID: 25117323
[TBL] [Abstract][Full Text] [Related]
10. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.
Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A
Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115
[TBL] [Abstract][Full Text] [Related]
11. Novel PTCH1 mutations in Japanese Nevoid basal cell carcinoma syndrome patients: two familial and three sporadic cases including the first Japanese patient with medulloblastoma.
Fujii M; Noguchi K; Urade M; Muraki Y; Moridera K; Kishimoto H; Hashimoto-Tamaoki T; Nakano Y
J Hum Genet; 2011 Apr; 56(4):277-83. PubMed ID: 21368767
[TBL] [Abstract][Full Text] [Related]
12. [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].
Mazzuoccolo LD; Martínez MF; Muchnik C; Azurmendi PJ; Stengel F
Medicina (B Aires); 2014; 74(4):307-10. PubMed ID: 25188659
[TBL] [Abstract][Full Text] [Related]
13. Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome.
Song YL; Zhang WF; Peng B; Wang CN; Wang Q; Bian Z
Tumour Biol; 2006; 27(4):175-80. PubMed ID: 16675912
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Nevoid basal cell carcinoma syndrome - clinical manifestations and mutation analysis of a Taiwanese family.
Chung CH; Wong TY; Shieh TY; Shieh DB; Chao SC
J Formos Med Assoc; 2003 Nov; 102(11):793-7. PubMed ID: 14724726
[TBL] [Abstract][Full Text] [Related]
16. Nevoid basal cell carcinoma syndrome (Gorlin syndrome).
Lo Muzio L
Orphanet J Rare Dis; 2008 Nov; 3():32. PubMed ID: 19032739
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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. PubMed ID: 22559979
[TBL] [Abstract][Full Text] [Related]
19. A new mutation of PTCH gene in a Chinese family with nevoid basal cell carcinoma syndrome.
Lü Y; Zhu HG; Ye WM; Zhang MB; He D; Chen WT
Chin Med J (Engl); 2008 Jan; 121(2):118-21. PubMed ID: 18272036
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]