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235 related items for PubMed ID: 27510672
1. 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 [Abstract] [Full Text] [Related]
2. Expression of calretinin in odontogenic keratocysts and basal cell carcinomas: A study of sporadic and Gorlin-Goltz syndrome-related cases. Cesinaro AM, Burtini G, Maiorana A, Rossi G, Migaldi M. Ann Diagn Pathol; 2020 Apr; 45():151472. PubMed ID: 31982676 [Abstract] [Full Text] [Related]
3. Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosis. Hubacek M, Kripnerova T, Nemcikova M, Krepelová A, Puchmajerova A, Malikova M, Havlovicová M, Cadova J, Kodet R, Macek M, Dostalova T. Neuro Endocrinol Lett; 2016 Sep; 37(4):269-276. PubMed ID: 27857042 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
12. Delayed Diagnosis of Gorlin-Goltz Syndrome: The Importance of the Multidisciplinary Approach. Figueira JA, Batista FRS, Rosso K, Veltrini VC, Pavan AJ. J Craniofac Surg; 2018 Sep; 29(6):e530-e531. PubMed ID: 29521748 [Abstract] [Full Text] [Related]
13. Gorlin-Goltz Syndrome - A Rare Case Entity in Young Child. Mondal S, Jain NK, Dutta A, Nishant, Dutta A, Shil M, Sen S. Prague Med Rep; 2024 Sep; 125(1):69-78. PubMed ID: 38470440 [Abstract] [Full Text] [Related]
14. Retrospective analysis of the histopathologic features of basal cell carcinomas in pediatric patients with basal cell nevus syndrome. Nguyen CV, Rubin AI, Smith A, Castelo-Soccio L. J Cutan Pathol; 2021 Mar; 48(3):390-395. PubMed ID: 33063358 [Abstract] [Full Text] [Related]
15. 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]
16. 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]
18. Simultaneous adenomatoid odontogenic and keratocystic odontogenic tumours in a patient with Gorlin-Goltz syndrome. Shephard M, Coleman H. Aust Dent J; 2014 Mar 22; 59(1):121-4. PubMed ID: 24588311 [Abstract] [Full Text] [Related]
19. [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 Mar 22; 74(4):307-10. PubMed ID: 25188659 [Abstract] [Full Text] [Related]
20. Basal cell nevus syndrome: clinical and molecular review and case report. Pino LC, Balassiano LK, Sessim M, de Almeida AP, Empinotti VD, Semenovitch I, Treu C, Lupi O. Int J Dermatol; 2016 Apr 22; 55(4):367-75. PubMed ID: 26356331 [Abstract] [Full Text] [Related] Page: [Next] [New Search]