Zuntini R - Search Results

1

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: zuntini r. 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.

2

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.

Gasparre G, Iommarini L, Porcelli AM, Lang M, Ferri GG, Kurelac I, Zuntini R, Mariani E, Pennisi LF, Pasquini E, Pasquinelli G, Ghelli A, Bonora E, Ceccarelli C, Rugolo M, Salfi N, Romeo G, Carelli V. Gasparre G, et al. Among authors: zuntini r. Hum Mutat. 2009 Mar;30(3):391-6. doi: 10.1002/humu.20870. Hum Mutat. 2009. PMID: 19086058

3

Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma.

Guerra F, Kurelac I, Cormio A, Zuntini R, Amato LB, Ceccarelli C, Santini D, Cormio G, Fracasso F, Selvaggi L, Resta L, Attimonelli M, Gadaleta MN, Gasparre G. Guerra F, et al. Among authors: zuntini r. Hum Mol Genet. 2011 Jun 15;20(12):2394-405. doi: 10.1093/hmg/ddr146. Epub 2011 Apr 5. Hum Mol Genet. 2011. PMID: 21470976

4

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. Among authors: zuntini r. 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

5

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. Among authors: zuntini r. 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.

6

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. Among authors: zuntini r. BMC Cancer. 2014 Feb 6;14:70. doi: 10.1186/1471-2407-14-70. BMC Cancer. 2014. PMID: 24498881 Free PMC article.

7

BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype.

Zuntini R, Cortesi L, Calistri D, Pippucci T, Martelli PL, Casadio R, Capizzi E, Santini D, Miccoli S, Medici V, Danesi R, Marchi I, Zampiga V, Fiorentino M, Ferrari S, Turchetti D. Zuntini R, et al. Oncotarget. 2017 Apr 4;8(14):22640-22648. doi: 10.18632/oncotarget.15151. Oncotarget. 2017. PMID: 28186987 Free PMC article.

8

Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients.

Ciavarella M, Miccoli S, Prossomariti A, Pippucci T, Bonora E, Buscherini F, Palombo F, Zuntini R, Balbi T, Ceccarelli C, Bazzoli F, Ricciardiello L, Turchetti D, Piazzi G. Ciavarella M, et al. Among authors: zuntini r. Eur J Hum Genet. 2018 Mar;26(3):387-395. doi: 10.1038/s41431-017-0086-y. Epub 2018 Jan 24. Eur J Hum Genet. 2018. PMID: 29367705 Free PMC article.

9

Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?

Zuntini R, Ferrari S, Bonora E, Buscherini F, Bertonazzi B, Grippa M, Godino L, Miccoli S, Turchetti D. Zuntini R, et al. Front Genet. 2018 Sep 11;9:378. doi: 10.3389/fgene.2018.00378. eCollection 2018. Front Genet. 2018. PMID: 30254663 Free PMC article.

10

BRCA2 in Ovarian Development and Function.

Turchetti D, Zuntini R, Tricarico R, Bellacosa A. Turchetti D, et al. Among authors: zuntini r. N Engl J Med. 2019 Mar 14;380(11):1086-1087. doi: 10.1056/NEJMc1813800. N Engl J Med. 2019. PMID: 30865813 No abstract available.

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