Ponti G - Search Results

1

Clinical utility gene card for: Gorlin syndrome--update 2013.

Lo Muzio L, Pastorino L, Levanat S, Musani V, Situm M, Ponti G, Bianchi Scarra G. Lo Muzio L, et al. Among authors: ponti g. Eur J Hum Genet. 2013 Oct;21(10). doi: 10.1038/ejhg.2012.299. Epub 2013 Jan 30. Eur J Hum Genet. 2013. PMID: 23361221 Free PMC article. No abstract available.

2

Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.

Ponti G, Nasti S, Losi L, Pastorino L, Pollio A, Benassi L, Giudice S, Bertazzoni G, Veratti E, Azzoni P, Bianchi Scarrà G, Seidenari S. Ponti G, et al. J Cutan Pathol. 2012 Mar;39(3):366-71. doi: 10.1111/j.1600-0560.2011.01813.x. Epub 2011 Nov 12. J Cutan Pathol. 2012. PMID: 22077640 Clinical Trial.

3

Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome.

Ponti G, Pollio A, Mignogna MD, Pellacani G, Pastorino L, Bianchi-Scarrà G, Di Gregorio C, Magnoni C, Azzoni P, Greco M, Seidenari S. Ponti G, et al. Cancer Genet. 2012 Apr;205(4):177-81. doi: 10.1016/j.cancergen.2012.01.012. Cancer Genet. 2012. PMID: 22559979

4

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. Ponti G, et al. Fam Cancer. 2012 Sep;11(3):411-8. doi: 10.1007/s10689-012-9529-3. Fam Cancer. 2012. PMID: 22565648

5

Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome.

Pastorino L, Pollio A, Pellacani G, Guarneri C, Ghiorzo P, Longo C, Bruno W, Giusti F, Bassoli S, Bianchi-Scarrà G, Ruini C, Seidenari S, Tomasi A, Ponti G. Pastorino L, et al. Among authors: ponti g. PLoS One. 2012;7(8):e43827. doi: 10.1371/journal.pone.0043827. Epub 2012 Aug 27. PLoS One. 2012. PMID: 22952776 Free PMC article.

6

Hereditary trichilemmal cysts: a proposal for the assessment of diagnostic clinical criteria.

Seidenari S, Pellacani G, Nasti S, Tomasi A, Pastorino L, Ghiorzo P, Ruini C, Bianchi-Scarrà G, Pollio A, Mandel VD, Ponti G. Seidenari S, et al. Among authors: ponti g. Clin Genet. 2013 Jul;84(1):65-9. doi: 10.1111/cge.12040. Epub 2012 Nov 8. Clin Genet. 2013. PMID: 23061468 Free article.

7

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome.

Ponti G, Tomasi A, Pastorino L, Ruini C, Guarneri C, Mandel VD, Seidenari S, Pellacani G. Ponti G, et al. Hered Cancer Clin Pract. 2012 Oct 29;10(1):15. doi: 10.1186/1897-4287-10-15. Hered Cancer Clin Pract. 2012. PMID: 23107377 Free PMC article.

8

Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.

Ponti G, Bertazzoni G, Pastorino L, Monari E, Cuoghi A, Bergamini S, Bellei E, Benassi L, Azzoni P, Petrachi T, Magnoni C, Pellacani G, Loschi P, Pollio A, Witkowski AM, Tomasi A. Ponti G, et al. Biomed Res Int. 2013;2013:794028. doi: 10.1155/2013/794028. Epub 2013 Dec 4. Biomed Res Int. 2013. PMID: 24369017 Free PMC article.

9

Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLD mutation in Brenner tumor.

Ponti G, Ruini C, Girolomoni G, Pellacani G, Farnetani F, Pastorino L, Ghiorzo P, Witkowski AM, Bianchi-Scarrà G, Tomasi A, Loschi P, Nasti S. Ponti G, et al. Future Oncol. 2014 Feb;10(3):345-50. doi: 10.2217/fon.13.198. Future Oncol. 2014. PMID: 24559443

10

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. Ponti G, et al. Future Oncol. 2014 May;10(6):917-25. doi: 10.2217/fon.14.2. Future Oncol. 2014. PMID: 24941978 Free article.

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