BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 19795138)

  • 1. Basal cell nevus syndrome: clinical and genetic diagnosis.
    García de Marcos JA; Dean-Ferrer A; Arroyo Rodríguez S; Calderón-Polanco J; Alamillos Granados FJ; Poblet E
    Oral Maxillofac Surg; 2009 Dec; 13(4):225-30. PubMed ID: 19795138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Clinical and genetic study in 22 patients with basal cell nevus syndrome].
    Pruvost-Balland C; Gorry P; Boutet N; Magnaldo T; Mamelle G; Margulis A; Kolb F; Duvillard P; Spatz A; Brugières L; Chompret A; Avril MF
    Ann Dermatol Venereol; 2006 Feb; 133(2):117-23. PubMed ID: 16508594
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Basal Cell Nevus (Gorlin) Syndrome with a Novel Heterozygous Deletion Frameshift Mutation (C.959delc, P.val322 Phe Fsx2) in the Ptch1 Gene Associated with Epiretinal Membrane, Odontogenic Keratocysts and without Skin Lesions and Falx Cerebri Calcification.
    Akaltun A; Eroz R; Dogan M; Bolu S; Onder HI; Onbas O; Kocabay K
    Genet Couns; 2016; 27(2):259-62. PubMed ID: 29485834
    [No Abstract]   [Full Text] [Related]  

  • 5. PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients.
    Li TJ; Yuan JW; Gu XM; Sun LS; Zhao HS
    Oral Dis; 2008 Mar; 14(2):174-9. PubMed ID: 18302678
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Novel mutations in the PATCHED gene in basal cell nevus syndrome.
    Lam CW; Leung CY; Lee KC; Xie J; Lo FM; Au TS; Tong SF; Poon MK; Chan LY; Luk NM
    Mol Genet Metab; 2002 May; 76(1):57-61. PubMed ID: 12175781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 58(1-2):43-53. PubMed ID: 19234436
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Manifestations of Gorlin-Goltz syndrome.
    Larsen AK; Mikkelsen DB; Hertz JM; Bygum A
    Dan Med J; 2014 May; 61(5):A4829. PubMed ID: 24814739
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome.
    Wang W; Wang J; Li J; Mao L; Guo F; Zhang B
    Br J Oral Maxillofac Surg; 2009 Jul; 47(5):366-9. PubMed ID: 19008023
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Nevoid basal cell carcinoma (Gorlin) syndrome.
    Gorlin RJ
    Genet Med; 2004; 6(6):530-9. PubMed ID: 15545751
    [No Abstract]   [Full Text] [Related]  

  • 13. Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations.
    Hashmi AA; Edhi MM; Faridi N; Hosein M; Khan M
    BMC Res Notes; 2016 Jul; 9():357. PubMed ID: 27448602
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [From gene to disease: basal cell naevus syndrome].
    de Meij TG; Baars MJ; Gille JJ; Hack WW; Haasnoot K; van Hagen JM
    Ned Tijdschr Geneeskd; 2005 Jan; 149(2):78-81. PubMed ID: 15688838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation.
    Ponti G; Ruini C; Pastorino L; Loschi P; Pecchi A; Malagoli M; Mandel VD; Boano R; Conti A; Pellacani G; Tomasi A
    Future Oncol; 2014 May; 10(6):917-25. PubMed ID: 24941978
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
    Pastorino L; Cusano R; Nasti S; Faravelli F; Forzano F; Baldo C; Barile M; Gliori S; Muggianu M; Ghigliotti G; Lacaita MG; Lo Muzio L; Bianchi-Scarra G
    Hum Mutat; 2005 Mar; 25(3):322-3. PubMed ID: 15712338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome.
    Ponti G; Pastorino L; Pollio A; Nasti S; Pellacani G; Mignogna MD; Tomasi A; Del Forno C; Longo C; Bianchi-Scarrà G; Ficarra G; Seidenari S
    Fam Cancer; 2012 Sep; 11(3):411-8. PubMed ID: 22565648
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors.
    Sun LS; Li XF; Li TJ
    J Dent Res; 2008 Jun; 87(6):575-9. PubMed ID: 18502968
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.