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Journal Abstract Search

162 related items for PubMed ID: 37564720

  • 1. Gorlin-Goltz Syndrome: A Case Report and Literature Review with PTCH1 Gene Sequencing.
    Kim HS, Heo S, Kim KS, Choi J, Yang JY.
    Arch Plast Surg; 2023 Jul; 50(4):384-388. PubMed ID: 37564720
    [Abstract] [Full Text] [Related]

  • 2. Gorlin-Goltz syndrome.
    Şereflican B, Tuman B, Şereflican M, Halıcıoğlu S, Özyalvaçlı G, Bayrak S.
    Turk Pediatri Ars; 2017 Sep; 52(3):173-177. PubMed ID: 29062253
    [Abstract] [Full Text] [Related]

  • 3. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
    Barraud S, Delemer B, Poirsier-Violle C, Bouligand J, Mérol JC, Grange F, Higel-Chaufour B, Decoudier B, Zalzali M, Dwyer AA, Acierno JS, Pitteloud N, Millar RP, Young J.
    Neuroendocrinology; 2021 Sep; 111(1-2):99-114. PubMed ID: 32074614
    [Abstract] [Full Text] [Related]

  • 4. Gorlin-Goltz syndrome.
    Joshi PS, Deshmukh V, Golgire S.
    Dent Res J (Isfahan); 2012 Jan; 9(1):100-6. PubMed ID: 22363371
    [Abstract] [Full Text] [Related]

  • 5. Concurrent medulloblastoma and cardiac fibroma: a rare presentation of Gorlin-Goltz syndrome.
    Alanazi R, Alkhaibary A, Alfaqawwy W, AlSufiani F, Ahmad N, Aljared T.
    Childs Nerv Syst; 2023 Sep; 39(9):2499-2504. PubMed ID: 37160435
    [Abstract] [Full Text] [Related]

  • 6. Ocular manifestations in Gorlin-Goltz syndrome.
    Moramarco A, Himmelblau E, Miraglia E, Mallone F, Roberti V, Franzone F, Iacovino C, Giustini S, Lambiase A.
    Orphanet J Rare Dis; 2019 Sep 18; 14(1):218. PubMed ID: 31533758
    [Abstract] [Full Text] [Related]

  • 7. Genetic mutations in Gorlin-Goltz syndrome.
    Daneswari M, Reddy MS.
    Indian J Hum Genet; 2013 Jul 18; 19(3):369-72. PubMed ID: 24339558
    [Abstract] [Full Text] [Related]

  • 8. Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome.
    Yue HT, Cao HY, He M.
    Chin J Dent Res; 2024 Mar 28; 27(1):83-88. PubMed ID: 38546523
    [Abstract] [Full Text] [Related]

  • 9. Gorlin syndrome (nevoid basal cell carcinoma syndrome): update and literature review.
    Fujii K, Miyashita T.
    Pediatr Int; 2014 Oct 28; 56(5):667-74. PubMed ID: 25131638
    [Abstract] [Full Text] [Related]

  • 10. Successful Radiotherapy for Metastatic Basal Cell Carcinoma to the Parotid Gland in a Patient With Gorlin-Goltz Syndrome.
    Neaga S, Beiu C, Popa LG, Orlov Slavu CM, Anghel AW.
    Cureus; 2024 Aug 28; 16(8):e67152. PubMed ID: 39295706
    [Abstract] [Full Text] [Related]

  • 11. Gorlin-Goltz Syndrome: A Case Report and Literature Review.
    Al-Jarboua MN, Al-Husayni AH, Al-Mgran M, Al-Omar AF.
    Cureus; 2019 Jan 08; 11(1):e3849. PubMed ID: 30891389
    [Abstract] [Full Text] [Related]

  • 12. [Gorlin-Goltz syndrome: review of the neuroradiological and maxillofacial features illustrated with two clinical cases].
    Safronova MM, Arantes M, Lima I, Domingues S, Almeida M, Moniz P.
    Acta Med Port; 2010 Jan 08; 23(6):1119-26. PubMed ID: 21627888
    [Abstract] [Full Text] [Related]

  • 13. Gorlin-Goltz Syndrome: A Rare Case Report of a 11-Year-Old Child.
    Tandon S, Chauhan Y, Sharma M, Jain M.
    Int J Clin Pediatr Dent; 2016 Jan 08; 9(3):264-268. PubMed ID: 27843260
    [Abstract] [Full Text] [Related]

  • 14. Nevoid Basal Cell Carcinoma Syndrome: PTCH1 Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients.
    Martinez MF, Romano MV, Martinez AP, González A, Muchnik C, Stengel FM, Mazzuoccolo LD, Azurmendi PJ.
    Cells; 2019 Feb 11; 8(2):. PubMed ID: 30754660
    [Abstract] [Full Text] [Related]

  • 15. Gorlin-Goltz syndrome with situs oppositus.
    Guruprasad Y, Prabhu PR.
    Natl J Maxillofac Surg; 2010 Jan 11; 1(1):58-62. PubMed ID: 22442553
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Exploration of the causative gene in a case of multiple nevoid basal cell carcinoma: A case report.
    Liu Y, Gao X, Cao L, Ren J, Miao Y, Cai X.
    Rare Tumors; 2024 Jul 25; 16():20363613241290394. PubMed ID: 39399445
    [Abstract] [Full Text] [Related]

  • 18. 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 20; 32(36):4155-61. PubMed ID: 25403219
    [Abstract] [Full Text] [Related]

  • 19. Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families.
    Kolkiran A, Şimşek-Kiper PÖ, Topaloğlu Yasan G, Karaosmanoğlu B, Taşkıran E, Utine GE, Tüz HH, Boduroğlu K.
    Mol Syndromol; 2024 Jun 20; 15(3):175-184. PubMed ID: 38841331
    [Abstract] [Full Text] [Related]

  • 20. Gorlin-Goltz syndrome: incidental finding on routine ct scan following car accident.
    Kalogeropoulou C, Zampakis P, Kazantzi S, Kraniotis P, Mastronikolis NS.
    Cases J; 2009 Nov 25; 2():9087. PubMed ID: 20062724
    [Abstract] [Full Text] [Related]

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