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Frequency of RET mutations in long- and short-segment Hirschsprung disease.
Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8.
Hum Mutat. 1997.
PMID: 9090527
A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.
Seri M, Celli I, Betsos N, Claudiani F, Camera G, Romeo G.
Seri M, et al. Among authors: celli i.
Clin Genet. 1997 Feb;51(2):86-90. doi: 10.1111/j.1399-0004.1997.tb02425.x.
Clin Genet. 1997.
PMID: 9111993
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A method for point mutation analysis that links SSCP and dye primer fluorescent sequencing.
Chiarelli I, Porfirio B, Mattiuz PL, Seri M, Caroli F, Celli I, Romeo G, Volorio S, Zollo M.
Chiarelli I, et al. Among authors: celli i.
Mol Cell Probes. 1998 Jun;12(3):125-31. doi: 10.1006/mcpr.1998.0159.
Mol Cell Probes. 1998.
PMID: 9664573
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The Correlation between Morpho-Dynamic Contrast-Enhanced Mammography (CEM) Features and Prognostic Factors in Breast Cancer: A Single-Center Retrospective Analysis.
Piccolo CL, Celli I, Bandini C, Tommasiello M, Sammarra M, Faggioni L, Cioni D, Beomonte Zobel B, Neri E.
Piccolo CL, et al. Among authors: celli i.
Cancers (Basel). 2024 Feb 22;16(5):870. doi: 10.3390/cancers16050870.
Cancers (Basel). 2024.
PMID: 38473232
Free PMC article.
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Isolated rupture of renal pelvis after blunt chest trauma: First description of a case.
Cirimele V, D'Amone G, Celli I, Campana G, Dirawe D, Pillitteri M, Perillo G, Faiella E, Beomonte Zobel B, Augusto Mallio C.
Cirimele V, et al. Among authors: celli i.
Radiol Case Rep. 2023 Aug 9;18(10):3479-3482. doi: 10.1016/j.radcr.2023.07.032. eCollection 2023 Oct.
Radiol Case Rep. 2023.
PMID: 37588238
Free PMC article.
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