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MSH2 Overexpression Due to an Unclassified Variant in 3'-Untranslated Region in a Patient with Colon Cancer.
Biomedicines. 2020 Jun 19;8(6):167. doi: 10.3390/biomedicines8060167.
Biomedicines. 2020.
PMID: 32575404
Free PMC article.
Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.
Liccardo R, Lambiase M, Nolano A, De Rosa M, Izzo P, Duraturo F.
Liccardo R, et al. Among authors: nolano a.
Int J Mol Med. 2022 Jun;49(6):81. doi: 10.3892/ijmm.2022.5137. Epub 2022 Apr 27.
Int J Mol Med. 2022.
PMID: 35475445
Free PMC article.
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Hypermethioninemia in Campania: Results from 10 years of newborn screening.
Villani GRD, Albano L, Caterino M, Crisci D, Di Tommaso S, Fecarotta S, Fisco MG, Frisso G, Gallo G, Mazzaccara C, Marchese E, Nolano A, Parenti G, Pecce R, Redi A, Salvatore F, Strisciuglio P, Turturo MG, Vallone F, Ruoppolo M.
Villani GRD, et al. Among authors: nolano a.
Mol Genet Metab Rep. 2019 Oct 11;21:100520. doi: 10.1016/j.ymgmr.2019.100520. eCollection 2019 Dec.
Mol Genet Metab Rep. 2019.
PMID: 31641591
Free PMC article.
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Germline Variants in MLH1 and ATM Genes in a Young Patient with MSI-H in a Precancerous Colonic Lesion.
Nolano A, Rossi GB, D'Angelo V, Liccardo R, Rosa M, Izzo P, Duraturo F.
Nolano A, et al.
Int J Mol Sci. 2023 Mar 22;24(6):5970. doi: 10.3390/ijms24065970.
Int J Mol Sci. 2023.
PMID: 36983044
Free PMC article.
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Hereditary Colorectal Cancer: State of the Art in Lynch Syndrome.
Nolano A, Medugno A, Trombetti S, Liccardo R, De Rosa M, Izzo P, Duraturo F.
Nolano A, et al.
Cancers (Basel). 2022 Dec 23;15(1):75. doi: 10.3390/cancers15010075.
Cancers (Basel). 2022.
PMID: 36612072
Free PMC article.
Review.
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