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Year | Number of Results |
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2011 | 1 |
2012 | 1 |
2013 | 1 |
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2021 | 3 |
2024 | 0 |
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Page 1
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
Int J Mol Sci. 2021 May 29;22(11):5832. doi: 10.3390/ijms22115832.
Int J Mol Sci. 2021.
PMID: 34072463
Free PMC article.
Review.
Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review.
Innella G, Miccoli S, Colussi D, Pradella LM, Amato LB, Zuntini R, Salfi NCM, Collina G, Ferrara F, Ricciardiello L, Turchetti D.
Innella G, et al. Among authors: pradella lm.
Pathol Res Pract. 2021 Feb;218:153339. doi: 10.1016/j.prp.2020.153339. Epub 2021 Jan 8.
Pathol Res Pract. 2021.
PMID: 33482532
Review.
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PTEN Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis.
Innella G, Bonora E, Neri I, Virdi A, Guglielmo A, Pradella LM, Ceccarelli C, Amato LB, Lanzoni A, Miccoli S, Gasparre G, Zuntini R, Turchetti D.
Innella G, et al. Among authors: pradella lm.
Front Med (Lausanne). 2021 Jul 27;8:688105. doi: 10.3389/fmed.2021.688105. eCollection 2021.
Front Med (Lausanne). 2021.
PMID: 34386506
Free PMC article.
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Where Birt-Hogg-Dubé meets Cowden syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours.
Pradella LM, Lang M, Kurelac I, Mariani E, Guerra F, Zuntini R, Tallini G, MacKay A, Reis-Filho JS, Seri M, Turchetti D, Gasparre G.
Pradella LM, et al.
Eur J Hum Genet. 2013 Oct;21(10):1169-72. doi: 10.1038/ejhg.2013.8. Epub 2013 Feb 6.
Eur J Hum Genet. 2013.
PMID: 23386036
Free PMC article.
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A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer.
Pradella LM, Evangelisti C, Ligorio C, Ceccarelli C, Neri I, Zuntini R, Amato LB, Ferrari S, Martelli AM, Gasparre G, Turchetti D.
Pradella LM, et al.
BMC Cancer. 2014 Feb 6;14:70. doi: 10.1186/1471-2407-14-70.
BMC Cancer. 2014.
PMID: 24498881
Free PMC article.
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Collective evidence supports neutrality of BRCA1 V1687I, a novel sequence variant in the conserved THV motif of the first BRCT repeat.
Cortesi L, De Nicolo A, Medici V, Marino M, Turchetti D, Pradella LM, Rossi G, Parisini E, Federico M.
Cortesi L, et al. Among authors: pradella lm.
Breast Cancer Res Treat. 2012 Jul;134(1):435-41. doi: 10.1007/s10549-012-2052-2. Epub 2012 Apr 22.
Breast Cancer Res Treat. 2012.
PMID: 22527099
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Two distinct thyroid tumours in a patient with Cowden syndrome carrying both a 10q23 and a mitochondrial DNA germline deletion.
Pradella LM, Zuntini R, Magini P, Ceccarelli C, Neri I, Cerasoli S, Graziano C, Gasparre G, Turchetti D.
Pradella LM, et al.
J Med Genet. 2011 Nov;48(11):779-82. doi: 10.1136/jmedgenet-2011-100152. Epub 2011 Sep 16.
J Med Genet. 2011.
PMID: 21926107
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