Franzoni A - Search Results

Year	Number of Results
1949	1
1955	1
1963	1
1965	1
1966	1
1967	1
1968	2
1969	2
1970	4
1980	1
2009	2
2010	3
2011	3
2012	3
2013	4
2014	3
2015	2
2016	2
2017	4
2018	3
2020	6
2021	5
2022	5
2023	5
2024	2
2025	4

1

A CGH array procedure to detect PAX6 gene structural defects.

Franzoni A, Russo PD, Baldan F, D'Elia AV, Puppin C, Penco S, Damante G. Franzoni A, et al. Mol Cell Probes. 2017 Apr;32:65-68. doi: 10.1016/j.mcp.2016.12.001. Epub 2016 Dec 2. Mol Cell Probes. 2017. PMID: 27919838

2

A polymorphic GGC repeat in the NPAS2 gene and its association with melanoma.

Franzoni A, Markova-Car E, Dević-Pavlić S, Jurišić D, Puppin C, Mio C, De Luca M, Petruz G, Damante G, Pavelić SK. Franzoni A, et al. Exp Biol Med (Maywood). 2017 Sep;242(15):1553-1558. doi: 10.1177/1535370217724093. Epub 2017 Aug 11. Exp Biol Med (Maywood). 2017. PMID: 28799406 Free PMC article.

3

A spotlight on analytical prospects in food allergens: From emerging allergens and novel foods to bioplastics and plant-based sustainable food contact materials.

Cavazza A, Mattarozzi M, Franzoni A, Careri M. Cavazza A, et al. Among authors: franzoni a. Food Chem. 2022 Sep 15;388:132951. doi: 10.1016/j.foodchem.2022.132951. Epub 2022 Apr 12. Food Chem. 2022. PMID: 35447585 Review.

4

A Prenatal Diagnosis of Verheij Syndrome in a Fetus Harboring a de novo PUF60 Variant.

Mio C, Orsaria M, Franzoni A, Bregant E, Betto E, Zucco J, Demori E, Damante G, Faletra F. Mio C, et al. Among authors: franzoni a. Clin Case Rep. 2025 Oct 15;13(10):e71230. doi: 10.1002/ccr3.71230. eCollection 2025 Oct. Clin Case Rep. 2025. PMID: 41113311 Free PMC article.

5

A bird's eye view on the use of whole exome sequencing in rare congenital ophthalmic diseases.

Zucco J, Baldan F, Allegri L, Bregant E, Passon N, Franzoni A, D'Elia AV, Faletra F, Damante G, Mio C. Zucco J, et al. Among authors: franzoni a. J Hum Genet. 2024 Jun;69(6):271-282. doi: 10.1038/s10038-024-01237-6. Epub 2024 Mar 8. J Hum Genet. 2024. PMID: 38459225 Free PMC article.

6

Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy.

Gnan C, Franzoni A, Baldan F, Passon N, Damante G, Dello Russo P. Gnan C, et al. Among authors: franzoni a. Mol Syndromol. 2017 Mar;8(2):98-102. doi: 10.1159/000454725. Epub 2017 Jan 17. Mol Syndromol. 2017. PMID: 28611550 Free PMC article.

7

A 16q deletion involving FOXF1 enhancer is associated to pulmonary capillary hemangiomatosis.

Dello Russo P, Franzoni A, Baldan F, Puppin C, De Maglio G, Pittini C, Cattarossi L, Pizzolitto S, Damante G. Dello Russo P, et al. Among authors: franzoni a. BMC Med Genet. 2015 Oct 13;16:94. doi: 10.1186/s12881-015-0241-7. BMC Med Genet. 2015. PMID: 26462560 Free PMC article.

8

Chlamydia trachomatis conjunctivitis in a male teenager: a case report.

Sulis G, Urbinati L, Franzoni A, Gargiulo F, Carvalho AC, Matteelli A. Sulis G, et al. Among authors: franzoni a. Infez Med. 2014 Jun;22(2):140-3. Infez Med. 2014. PMID: 24955802 Free article.

9

Longitudinal profiling of hormone receptor positive, HER2 negative metastatic breast cancer through droplet digital PCR-based circulating tumor DNA fragmentomics.

Foffano L, Franzoni A, Molteni E, Giudici F, Dri A, Basile D, Cucciniello L, Buriolla S, Noto C, Russo S, Nascimbeni E, Bolzonello S, Pastò B, Rossa SD, Allegri L, Bonotto M, Minisini AM, Belletti B, Damante G, Gerratana L, Puglisi F. Foffano L, et al. Among authors: franzoni a. Transl Oncol. 2025 Sep;59:102456. doi: 10.1016/j.tranon.2025.102456. Epub 2025 Jun 26. Transl Oncol. 2025. PMID: 40577963 Free PMC article.

10

A new germline VHL gene mutation in three patients with apparently sporadic pheochromocytoma.

D'Elia AV, Grimaldi F, Pizzolitto S, De Maglio G, Bregant E, Passon N, Franzoni A, Verrienti A, Tamburrano G, Durante C, Filetti S, Fogolari F, Russo D, Damante G. D'Elia AV, et al. Among authors: franzoni a. Clin Endocrinol (Oxf). 2013 Mar;78(3):391-7. doi: 10.1111/cen.12032. Clin Endocrinol (Oxf). 2013. PMID: 22946750

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