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FACILITATE: A real-world, multicenter, prospective study investigating the utility of a rapid, fully automated real-time PCR assay versus local reference methods for detecting epidermal growth factor receptor variants in NSCLC.
Behnke A, Cayre A, De Maglio G, Giannini G, Habran L, Tarsitano M, Chetta M, Cappellen D, Lespagnol A, Le Naoures C, Massazza G, Destro A, Bonzheim I, Rau A, Battmann A, Kah B, Watkin E, Hummel M. Behnke A, et al. Among authors: chetta m. Pathol Oncol Res. 2023 Jan 31;29:1610707. doi: 10.3389/pore.2023.1610707. eCollection 2023. Pathol Oncol Res. 2023. PMID: 36798672 Free PMC article.
Neutrophil-to-Lymphocyte Ratio Is a Major Prognostic Factor in Non-small Cell Lung Carcinoma Patients Undergoing First Line Immunotherapy With Pembrolizumab.
Romano FJ, Ronga R, Ambrosio F, Arundine D, Longo V, Galetta D, Gridelli C, Maione P, Palma V, Damiano V, Verde A, Giacobbe I, Augurio MR, Iengo G, Chetta M, Tarsitano M, Campione S, Failla G, Raucci A, Riccardi F. Romano FJ, et al. Among authors: chetta m. Cancer Diagn Progn. 2023 Jan 3;3(1):44-52. doi: 10.21873/cdp.10178. eCollection 2023 Jan-Feb. Cancer Diagn Progn. 2023. PMID: 36632583 Free PMC article.
De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature.
Bukvic N, De Rinaldis M, Chetta M, Trabacca A, Bassi MT, Marsano RM, Holoubkova L, Rivieccio M, Oro M, Resta N, Kerkhof J, Sadikovic B, Viggiano L. Bukvic N, et al. Among authors: chetta m. Genes (Basel). 2024 Jun 22;15(7):826. doi: 10.3390/genes15070826. Genes (Basel). 2024. PMID: 39062605 Free PMC article. Review.
Venous Thromboembolism Prophylaxis in Plastic Surgery.
Gupta R, Bisht C, Genova R, Ege E, Chetta M, Shaheen K. Gupta R, et al. Among authors: chetta m. Eplasty. 2023 Dec 11;23:e78. eCollection 2023. Eplasty. 2023. PMID: 38229957 Free PMC article.
What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis.
Bukvic N, Chetta M, Bagnulo R, Leotta V, Pantaleo A, Palumbo O, Palumbo P, Oro M, Rivieccio M, Laforgia N, De Rinaldis M, Rosati A, Kerkhof J, Sadikovic B, Resta N. Bukvic N, et al. Among authors: chetta m. Genes (Basel). 2023 Jan 7;14(1):165. doi: 10.3390/genes14010165. Genes (Basel). 2023. PMID: 36672906 Free PMC article.
67 results