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Prevalence, Type, and Molecular Spectrum of NF1 Mutations in Patients with Neurofibromatosis Type 1 and Congenital Heart Disease.
Genes (Basel). 2019 Sep 4;10(9):675. doi: 10.3390/genes10090675.
Genes (Basel). 2019.
PMID: 31487937
Free PMC article.
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease.
Marongiu R, Ghezzi D, Ialongo T, Soleti F, Elia A, Cavone S, Albanese A, Altavista MC, Barone P, Brusa L, Cortelli P, Petrozzi L, Scaglione C, Stanzione P, Tinazzi M, Zeviani M, Dallapiccola B, Bentivoglio AR, Valente EM, Garavaglia B; Italian PD Study Group.
Marongiu R, et al. Among authors: cavone s.
Mov Disord. 2006 Aug;21(8):1232-5. doi: 10.1002/mds.20890.
Mov Disord. 2006.
PMID: 16622859
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Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer.
Tsongalis GJ, Al Turkmani MR, Suriawinata M, Babcock MJ, Mitchell K, Ding Y, Scicchitano L, Tira A, Buckingham L, Atkinson S, Lax A, Aisner DL, Davies KD, Wood HN, O'Neill SS, Levine EA, Sequeira J, Harada S, DeFrank G, Paluri R, Tan BA, Colabella H, Snead C, Cruz-Correa M, Ramirez V, Rojas A, Huang H, Mackinnon AC, Garcia FU, Cavone SM, Elfahal M, Abel G, Vasef MA, Judd A, Linder MW, Alkhateeb K, Skinner WL, Boccia R, Patel K.
Tsongalis GJ, et al. Among authors: cavone sm.
Am J Clin Pathol. 2020 Jul 7;154(2):266-276. doi: 10.1093/ajcp/aqaa044.
Am J Clin Pathol. 2020.
PMID: 32525522
Free PMC article.
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Diagnostic utility of p75 neurotrophin receptor (p75NTR) as a marker of breast myoepithelial cells.
Popnikolov NK, Cavone SM, Schultz PM, Garcia FU.
Popnikolov NK, et al. Among authors: cavone sm.
Mod Pathol. 2005 Dec;18(12):1535-41. doi: 10.1038/modpathol.3800487.
Mod Pathol. 2005.
PMID: 16258511
Free article.
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