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Year | Number of Results |
---|---|
2021 | 3 |
2023 | 3 |
2024 | 1 |
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Page 1
Spinal Muscular Atrophy: An Evolving Scenario through New Perspectives in Diagnosis and Advances in Therapies.
Int J Mol Sci. 2023 Oct 3;24(19):14873. doi: 10.3390/ijms241914873.
Int J Mol Sci. 2023.
PMID: 37834320
Free PMC article.
Review.
Clinical usefulness of NGS multi-gene panel testing in hereditary cancer analysis.
Anaclerio F, Pilenzi L, Dell'Elice A, Ferrante R, Grossi S, Ferlito LM, Marinelli C, Gildetti S, Calabrese G, Stuppia L, Antonucci I.
Anaclerio F, et al. Among authors: dell elice a.
Front Genet. 2023 Feb 1;14:1060504. doi: 10.3389/fgene.2023.1060504. eCollection 2023.
Front Genet. 2023.
PMID: 37065479
Free PMC article.
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Perinatal Tissue-Derived Stem Cells: An Emerging Therapeutic Strategy for Challenging Neurodegenerative Diseases.
Bruno A, Milillo C, Anaclerio F, Buccolini C, Dell'Elice A, Angilletta I, Gatta M, Ballerini P, Antonucci I.
Bruno A, et al. Among authors: dell elice a.
Int J Mol Sci. 2024 Jan 12;25(2):976. doi: 10.3390/ijms25020976.
Int J Mol Sci. 2024.
PMID: 38256050
Free PMC article.
Review.
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Lynch syndrome and Muir-Torre phenotype associated with a recurrent variant in the 3'UTR of the MSH6 gene.
Cini G, Carnevali I, Sahnane N, Chiaravalli AM, Dell'Elice A, Maestro R, Pin E, Bestetti I, Radovic S, Armelao F, Viel A, Tibiletti MG.
Cini G, et al. Among authors: dell elice a.
Cancer Genet. 2021 Jun;254-255:1-10. doi: 10.1016/j.cancergen.2021.01.005. Epub 2021 Jan 19.
Cancer Genet. 2021.
PMID: 33516942
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Filling the gap: A thorough investigation for the genetic diagnosis of unsolved polyposis patients with monoallelic MUTYH pathogenic variants.
Dell'Elice A, Cini G, Fornasarig M, Armelao F, Barana D, Bianchi F, Casalis Cavalchini GC, Maffè A, Mammi I, Pedroni M, Percesepe A, Sorrentini I, Tibiletti M, Maestro R, Quaia M, Viel A.
Dell'Elice A, et al.
Mol Genet Genomic Med. 2021 Dec;9(12):e1831. doi: 10.1002/mgg3.1831. Epub 2021 Oct 26.
Mol Genet Genomic Med. 2021.
PMID: 34704405
Free PMC article.
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Detection of Germline Mutations in a Cohort of 250 Relatives of Mutation Carriers in Multigene Panel: Impact of Pathogenic Variants in Other Genes beyond BRCA1/2.
Di Rado S, Giansante R, Cicirelli M, Pilenzi L, Dell'Elice A, Anaclerio F, Rimoldi M, Grassadonia A, Grossi S, Canale N, Ballerini P, Stuppia L, Antonucci I.
Di Rado S, et al. Among authors: dell elice a.
Cancers (Basel). 2023 Dec 6;15(24):5730. doi: 10.3390/cancers15245730.
Cancers (Basel). 2023.
PMID: 38136276
Free PMC article.
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Definition and management of colorectal polyposis not associated with APC/MUTYH germline pathogenic variants: AIFEG consensus statement.
Urso EDL, Ponz de Leon M, Vitellaro M, Piozzi GN, Bao QR, Martayan A, Remo A, Stigliano V, Oliani C, Lucci Cordisco E, Pucciarelli S, Ranzani GN, Viel A; AIFEG group.
Urso EDL, et al.
Dig Liver Dis. 2021 Apr;53(4):409-417. doi: 10.1016/j.dld.2020.11.018. Epub 2021 Jan 25.
Dig Liver Dis. 2021.
PMID: 33504457
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