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Anomalous vascularization in a Wnt medulloblastoma: a case report.
Di Giannatale A, Carai A, Cacchione A, Marrazzo A, Dell'Anna VA, Colafati GS, Diomedi-Camassei F, Miele E, Po A, Ferretti E, Locatelli F, Mastronuzzi A. Di Giannatale A, et al. Among authors: cacchione a. BMC Neurol. 2016 Jul 15;16:103. doi: 10.1186/s12883-016-0632-1. BMC Neurol. 2016. PMID: 27416922 Free PMC article.
Cancer Predisposition Syndromes and Medulloblastoma in the Molecular Era.
Carta R, Del Baldo G, Miele E, Po A, Besharat ZM, Nazio F, Colafati GS, Piccirilli E, Agolini E, Rinelli M, Lodi M, Cacchione A, Carai A, Boccuto L, Ferretti E, Locatelli F, Mastronuzzi A. Carta R, et al. Among authors: cacchione a. Front Oncol. 2020 Oct 29;10:566822. doi: 10.3389/fonc.2020.566822. eCollection 2020. Front Oncol. 2020. PMID: 33194646 Free PMC article. Review.
Medulloblastoma Associated with Down Syndrome: From a Rare Event Leading to a Pathogenic Hypothesis.
Boni A, Ranalli M, Del Baldo G, Carta R, Lodi M, Agolini E, Rinelli M, Valentini D, Rossi S, Alesi V, Cacchione A, Miele E, Alessi I, Caroleo AM, Colafati GS, De Ioris MA, Boccuto L, Balducci M, Carai A, Mastronuzzi A. Boni A, et al. Among authors: cacchione a. Diagnostics (Basel). 2021 Feb 7;11(2):254. doi: 10.3390/diagnostics11020254. Diagnostics (Basel). 2021. PMID: 33562188 Free PMC article.
Expansion of the clinical and molecular spectrum of an XPD-related disorder linked to biallelic mutations in ERCC2 gene.
Agolini E, Botta E, Lodi M, Digilio MC, Rinelli M, Bellacchio E, Alesi V, Nardo T, Zambruno G, Orioli D, Alessi I, Boccuto L, Rossi S, Carai A, Colafati GS, Cacchione A, Dallapiccola B, Novelli A, Mastronuzzi A. Agolini E, et al. Among authors: cacchione a. Clin Genet. 2021 Jun;99(6):842-848. doi: 10.1111/cge.13957. Epub 2021 Apr 5. Clin Genet. 2021. PMID: 33733458
Molecular Characterization of Medulloblastoma in a Patient with Neurofibromatosis Type 1: Case Report and Literature Review.
Ranalli M, Boni A, Caroleo AM, Del Baldo G, Rinelli M, Agolini E, Rossi S, Miele E, Colafati GS, Boccuto L, Alessi I, De Ioris MA, Cacchione A, Capolino R, Carai A, Vennarini S, Mastronuzzi A. Ranalli M, et al. Among authors: cacchione a. Diagnostics (Basel). 2021 Apr 2;11(4):647. doi: 10.3390/diagnostics11040647. Diagnostics (Basel). 2021. PMID: 33918520 Free PMC article.
ALK-rearranged histiocytosis: Report of two cases with involvement of the central nervous system.
Rossi S, Gessi M, Barresi S, Tamburrini G, Giovannoni I, Ruggiero A, Colafati GS, Frassanito P, Carboni A, Alexandre A, Cacchione A, Trombatore P, Diomedi-Camassei F, Gaspari S, Gianno F, Marras CE, Cecinati V, Carai A, Mastronuzzi A, Alaggio R. Rossi S, et al. Among authors: cacchione a. Neuropathol Appl Neurobiol. 2021 Oct;47(6):878-881. doi: 10.1111/nan.12739. Epub 2021 Jun 18. Neuropathol Appl Neurobiol. 2021. PMID: 34048085
Paediatric astroblastoma-like neuroepithelial tumour of the spinal cord with a MAMLD1-BEND2 rearrangement.
Rossi S, Barresi S, Colafati GS, Giovannoni I, Miele E, Alesi V, Cacchione A, Diomedi-Camassei F, Macari G, Antonelli M, Carboni A, Carai A, Mastronuzzi A, Giangaspero F, Gessi M, Alaggio R. Rossi S, et al. Among authors: cacchione a. Neuropathol Appl Neurobiol. 2022 Aug;48(5):e12814. doi: 10.1111/nan.12814. Epub 2022 Apr 10. Neuropathol Appl Neurobiol. 2022. PMID: 35301744
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic POLR2A variant.
Paparella R, Caroleo AM, Agolini E, Chillemi G, Miele E, Pedace L, Rinelli M, Pizzi S, Boccuto L, Colafati GS, Lodi M, Cacchione A, Carai A, Digilio MC, Tomà P, Tartaglia M, Mastronuzzi A. Paparella R, et al. Among authors: cacchione a. Am J Med Genet A. 2022 Sep;188(9):2796-2802. doi: 10.1002/ajmg.a.62869. Epub 2022 Jun 11. Am J Med Genet A. 2022. PMID: 35689525 Free PMC article.
67 results