Lo Muzio L - Search Results

1

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. Pastorino L, et al. Among authors: lo muzio l. Hum Mutat. 2005 Mar;25(3):322-3. doi: 10.1002/humu.9317. Hum Mutat. 2005. PMID: 15712338

2

Nevoid basal cell carcinoma syndrome. Clinical findings in 37 Italian affected individuals.

Lo Muzio L, Nocini PF, Savoia A, Consolo U, Procaccini M, Zelante L, Pannone G, Bucci P, Dolci M, Bambini F, Solda P, Favia G. Lo Muzio L, et al. Clin Genet. 1999 Jan;55(1):34-40. doi: 10.1034/j.1399-0004.1999.550106.x. Clin Genet. 1999. PMID: 10066029

3

Early diagnosis of nevoid basal cell carcinoma syndrome.

Lo Muzio L, Nocini P, Bucci P, Pannone G, Consolo U, Procaccini M. Lo Muzio L, et al. J Am Dent Assoc. 1999 May;130(5):669-74. doi: 10.14219/jada.archive.1999.0276. J Am Dent Assoc. 1999. PMID: 10332131

4

Multiple parotid lymphoepithelial cysts in patients with HIV-infection: report of two cases.

Favia G, Capodiferro S, Scivetti M, Lacaita MG, Filosa A, Lo Muzio L. Favia G, et al. Among authors: lo muzio l. Oral Dis. 2004 May;10(3):151-4. doi: 10.1046/j.1601-0825.2003.01006.x. Oral Dis. 2004. PMID: 15089924

5

Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.

Savino M, d'Apolito M, Formica V, Baorda F, Mari F, Renieri A, Carabba E, Tarantino E, Andreucci E, Belli S, Lo Muzio L, Dallapiccola B, Zelante L, Savoia A. Savino M, et al. Among authors: lo muzio l. Hum Mutat. 2004 Nov;24(5):441. doi: 10.1002/humu.9289. Hum Mutat. 2004. PMID: 15459969

6

Infected paradental cysts in children: a clinicopathological study of 15 cases.

Lacaita MG, Capodiferro S, Favia G, Santarelli A, Lo Muzio L. Lacaita MG, et al. Among authors: lo muzio l. Br J Oral Maxillofac Surg. 2006 Apr;44(2):112-5. doi: 10.1016/j.bjoms.2005.03.011. Epub 2005 Oct 3. Br J Oral Maxillofac Surg. 2006. PMID: 16203063

7

A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia.

Lo Muzio L, Tetè S, Mastrangelo F, Cazzolla AP, Lacaita MG, Margaglione M, Campisi G. Lo Muzio L, et al. Ann Clin Lab Sci. 2007 Spring;37(2):115-20. Ann Clin Lab Sci. 2007. PMID: 17522365

8

Nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Lo Muzio L. Lo Muzio L. Orphanet J Rare Dis. 2008 Nov 25;3:32. doi: 10.1186/1750-1172-3-32. Orphanet J Rare Dis. 2008. PMID: 19032739 Free PMC article. Review.

9

Clinical utility gene card for: Gorlin syndrome.

Lo Muzio L, Pastorino L, Levanat S, Musani V, Situm M, Scarra GB. Lo Muzio L, et al. Eur J Hum Genet. 2011 Aug;19(8). doi: 10.1038/ejhg.2011.9. Epub 2011 Feb 9. Eur J Hum Genet. 2011. PMID: 21304560 Free PMC article. No abstract available.

10

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. 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.

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