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Journal Abstract Search

188 related items for 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
    [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
    [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
    [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 Feb; 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
    [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
    [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 25; 13(3):5654-63. PubMed ID: 25117323
    [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 25; 76(1):57-61. PubMed ID: 12175781
    [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 May 25; 58(1-2):43-53. PubMed ID: 19234436
    [Abstract] [Full Text] [Related]

  • 10. Manifestations of Gorlin-Goltz syndrome.
    Larsen AK, Mikkelsen DB, Hertz JM, Bygum A.
    Dan Med J; 2014 May 25; 61(5):A4829. PubMed ID: 24814739
    [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 25; 47(5):366-9. PubMed ID: 19008023
    [Abstract] [Full Text] [Related]

  • 12. Nevoid basal cell carcinoma (Gorlin) syndrome.
    Gorlin RJ.
    Genet Med; 2004 Jul 25; 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 22; 9():357. PubMed ID: 27448602
    [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 08; 149(2):78-81. PubMed ID: 15688838
    [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 08; 10(6):917-25. PubMed ID: 24941978
    [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 08; 25(3):322-3. PubMed ID: 15712338
    [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 08; 11(3):411-8. PubMed ID: 22565648
    [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 08; 87(6):575-9. PubMed ID: 18502968
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 56(20):4599-601. PubMed ID: 8840969
    [Abstract] [Full Text] [Related]

  • 20. 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 Oct 15; 59(3):335-8. PubMed ID: 27510672
    [Abstract] [Full Text] [Related]

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