Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1995 3
1997 1
1998 1
1999 1
2001 1
2003 2
2004 1
2005 3
2006 1
2007 4
2008 3
2009 2
2010 4
2011 3
2012 4
2013 3
2015 1
2016 2
2017 2
2018 3
2019 1
2020 5
2021 5
2022 5
2023 3
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

61 results

Results by year

Filters applied: . Clear all
Page 1
Optical coherence tomography.
Ripandelli G, Coppé AM, Capaldo A, Stirpe M. Ripandelli G, et al. Among authors: coppe am. Semin Ophthalmol. 1998 Dec;13(4):199-202. doi: 10.3109/08820539809056053. Semin Ophthalmol. 1998. PMID: 9878670 Review.
A guilt-by-association mutation network in LGL leukemia.
Andersson EI, Coppe A, Bortoluzzi S. Andersson EI, et al. Among authors: coppe a. Oncotarget. 2017 Oct 9;8(55):93299-93300. doi: 10.18632/oncotarget.21699. eCollection 2017 Nov 7. Oncotarget. 2017. PMID: 29212142 Free PMC article. No abstract available.
A Novel Autosomal Recessive Variant of the NRL Gene Causing Enhanced S-Cone Syndrome: A Morpho-Functional Analysis of Two Unrelated Pediatric Patients.
Iarossi G, Sinibaldi L, Passarelli C, Coppe' AM, Cappelli A, Petrocelli G, Catena G, Perrone C, Falsini B, Novelli A, Bartuli A, Buzzonetti L. Iarossi G, et al. Among authors: coppe am. Diagnostics (Basel). 2022 Sep 9;12(9):2183. doi: 10.3390/diagnostics12092183. Diagnostics (Basel). 2022. PMID: 36140584 Free PMC article.
A high definition picture of key genes and pathways mutated in pediatric follicular lymphoma.
Lovisa F, Binatti A, Coppe A, Primerano S, Carraro E, Pillon M, Pizzi M, Guzzardo V, Buffardi S, Porta F, Farruggia P, De Santis R, Bulian P, Basso G, Lazzari E, d'Amore ESG, Bortoluzzi S, Mussolin L. Lovisa F, et al. Among authors: coppe a. Haematologica. 2019 Sep;104(9):e406-e409. doi: 10.3324/haematol.2018.211631. Epub 2019 Feb 28. Haematologica. 2019. PMID: 30819919 Free PMC article. No abstract available.
Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals.
Maltese PE, Colombo L, Martella S, Rossetti L, El Shamieh S, Sinibaldi L, Passarelli C, Coppè AM, Buzzonetti L, Falsini B, Chiurazzi P, Placidi G, Tanzi B, Bertelli M, Iarossi G. Maltese PE, et al. Among authors: coppe am. Front Genet. 2022 Jun 28;13:914345. doi: 10.3389/fgene.2022.914345. eCollection 2022. Front Genet. 2022. PMID: 35836572 Free PMC article.
61 results