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Did you mean alessandra stella (90 results)?
BRCA1 and BRCA2 Testing through Next Generation Sequencing in a Small Cohort of Italian Breast/Ovarian Cancer Patients: Novel Pathogenic and Unknown Clinical Significance Variants.
Concolino P, Gelli G, Rizza R, Costella A, Scambia G, Capoluongo E. Concolino P, et al. Among authors: costella a. Int J Mol Sci. 2019 Jul 12;20(14):3442. doi: 10.3390/ijms20143442. Int J Mol Sci. 2019. PMID: 31336956 Free PMC article.
CYP21A2 intronic variants causing 21-hydroxylase deficiency.
Concolino P, Rizza R, Costella A, Carrozza C, Zuppi C, Capoluongo E. Concolino P, et al. Among authors: costella a. Metabolism. 2017 Jun;71:46-51. doi: 10.1016/j.metabol.2017.03.003. Epub 2017 Mar 9. Metabolism. 2017. PMID: 28521877 Review.
Mutational Landscape of Resistance to Thyroid Hormone Beta (RTH╬▓).
Concolino P, Costella A, Paragliola RM. Concolino P, et al. Among authors: costella a. Mol Diagn Ther. 2019 Jun;23(3):353-368. doi: 10.1007/s40291-019-00399-w. Mol Diagn Ther. 2019. PMID: 30976996 Review.
A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis.
Concolino P, Rizza R, Mignone F, Costella A, Guarino D, Carboni I, Capoluongo E, Santonocito C, Urbani A, Minucci A. Concolino P, et al. Among authors: costella a. Clin Chim Acta. 2018 May;480:173-179. doi: 10.1016/j.cca.2018.02.012. Epub 2018 Feb 16. Clin Chim Acta. 2018. PMID: 29458049 No abstract available.
Preliminary molecular evidence associating a novel BRCA1 synonymous variant with hereditary ovarian cancer syndrome.
Minucci A, Concolino P, De Bonis M, Costella A, Paris I, Scambia G, Capoluongo E. Minucci A, et al. Among authors: costella a. Hum Genome Var. 2018 Apr 20;5:2. doi: 10.1038/s41439-018-0003-0. eCollection 2018. Hum Genome Var. 2018. PMID: 29760936 Free PMC article.
Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review.
Minucci A, Scambia G, Santonocito C, Concolino P, Canu G, Mignone F, Saggese I, Guarino D, Costella A, Molinario R, De Bonis M, Ferrandina G, Petrillo M, Scaglione GL, Capoluongo E. Minucci A, et al. Among authors: costella a. Expert Rev Mol Diagn. 2015;15(10):1383-403. doi: 10.1586/14737159.2015.1081059. Epub 2015 Aug 26. Expert Rev Mol Diagn. 2015. PMID: 26306726 Review.
Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years.
Concolino P, Costella A, Capoluongo E. Concolino P, et al. Among authors: costella a. Cancer Genet. 2016 Jan-Feb;209(1-2):36-41. doi: 10.1016/j.cancergen.2015.12.002. Epub 2015 Dec 14. Cancer Genet. 2016. PMID: 26767918 Review.
High-resolution melting analysis coupled with next-generation sequencing as a simple tool for the identification of a novel somatic BRCA2 variant: a case report.
Costella A, De Leo R, Guarino D, D'Indinosante M, Concolino P, Mazzuccato G, Urbani A, Scambia G, Capoluongo E, Fagotti A, Minucci A. Costella A, et al. Hum Genome Var. 2018 Jun 8;5:10. doi: 10.1038/s41439-018-0006-x. eCollection 2018. Hum Genome Var. 2018. PMID: 29899995 Free PMC article.
Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G>A/c.7008-2A>T genotype Response to: Nagy PL, Mansukhani M. The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations. Expert Rev Mol Diagn 2015;15(9):1101-5.
Minucci A, De Bonis M, Costella A, Scambia G, Scandurra G, Capoluongo E. Minucci A, et al. Among authors: costella a. Expert Rev Mol Diagn. 2016 Jul;16(7):715-7. doi: 10.1080/14737159.2016.1184573. Epub 2016 May 17. Expert Rev Mol Diagn. 2016. PMID: 27125725 No abstract available.
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