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Journal Abstract Search

329 related items for PubMed ID: 25131638

  • 21. [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; 23(6):1119-26. PubMed ID: 21627888
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  • 22. 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
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  • 27. Spontaneous recovery from a medulloblastoma by a female with Gorlin-Goltz syndrome.
    Su CW, Lin KL, Hou JW, Jung SM, Zen EC.
    Pediatr Neurol; 2003 Mar; 28(3):231-4. PubMed ID: 12770681
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  • 29. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome.
    Alonso N, Cañueto J, Ciria S, Bueno E, Palacios-Alvarez I, Alegre M, Badenas C, Barreiro A, Pena L, Maldonado C, Nespeira-Jato MV, Peña-Penabad C, Azon A, Gavrilova M, Ferrer I, Sanmartin O, Robles L, Hernandez-Martin A, Urioste M, Puig S, Puig L, Gonzalez-Sarmiento R.
    Br J Dermatol; 2018 Jan; 178(1):198-206. PubMed ID: 28733979
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  • 31. Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.
    Casano K, Meddaugh H, Zambrano RM, Marble M, Torres JI, Lacassie Y.
    Eur J Med Genet; 2020 Apr; 63(4):103842. PubMed ID: 31945512
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  • 32. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
    Musani V, Ozretić P, Trnski D, Sabol M, Poduje S, Tošić M, Šitum M, Levanat S.
    Croat Med J; 2018 Feb 28; 59(1):20-24. PubMed ID: 29498494
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  • 34. 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 28; 56(1):63-7. PubMed ID: 25727044
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  • 35. 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 28; 10(6):917-25. PubMed ID: 24941978
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  • 37. Gorlin syndrome or basal cell nevus syndrome (BCNS): A case report.
    Shivaswamy KN, Sumathy TK, Shyamprasad AL, Ranganathan C.
    Dermatol Online J; 2010 Sep 15; 16(9):6. PubMed ID: 20875327
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  • 38. Exploring the Changing Diagnostic Criteria of Gorlin-Goltz Syndrome: A Case Report.
    Shetty SK, Doddawad VG, Sundar S, S S.
    Oncology (Williston Park); 2023 Nov 08; 37(11):449-554. PubMed ID: 38032303
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  • 39. Nevoid basal cell carcinoma syndrome: our experience in a pediatric hospital.
    Samela PC, Tosi V, Cervini AB, Bocian M, Buján MM, Pierini AM.
    Actas Dermosifiliogr; 2013 Jun 08; 104(5):426-33. PubMed ID: 23669591
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