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
1991 1
1992 2
1994 2
1998 1
2001 2
2003 2
2004 1
2005 1
2006 2
2008 1
2011 1
2013 1
2014 1
2015 3
2016 1
2018 2
2019 3
2020 3
2021 3
2022 1
2023 4
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

35 results

Results by year

Filters applied: . Clear all
Page 1
Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies.
Cicinelli MV, Marchese A, Bordato A, Manitto MP, Bandello F, Battaglia Parodi M. Cicinelli MV, et al. Among authors: manitto mp. Ophthalmol Ther. 2020 Jun;9(2):249-263. doi: 10.1007/s40123-020-00241-1. Epub 2020 Mar 5. Ophthalmol Ther. 2020. PMID: 32141037 Free PMC article. Review.
BENIGN FOVEAL DEPIGMENTATION: A MULTIMODAL IMAGING INVESTIGATION.
Parodi MB, Arrigo A, Bruschi E, Manitto MP, Martina E, Bandello F. Parodi MB, et al. Among authors: manitto mp. Retin Cases Brief Rep. 2023 Jan 1;17(1):74-79. doi: 10.1097/ICB.0000000000001115. Retin Cases Brief Rep. 2023. PMID: 33395020
Nummular Macular Depigmentation in Dandy-Walker Syndrome.
Parodi MB, Arrigo A, Manitto MP, Bandello F. Parodi MB, et al. Among authors: manitto mp. Retina. 2020 Sep;40(9):e46-e47. doi: 10.1097/IAE.0000000000002887. Retina. 2020. PMID: 32658163 No abstract available.
Multimodal imaging in Schubert-Bornschein congenital stationary night blindness.
Parodi MB, Arrigo A, Rajabian F, Mansour A, Mercuri S, Starace V, Bordato A, Manitto MP, Martina E, Bandello F. Parodi MB, et al. Among authors: manitto mp. Ophthalmic Genet. 2023 Aug;44(4):408-413. doi: 10.1080/13816810.2022.2135108. Epub 2022 Oct 13. Ophthalmic Genet. 2023. PMID: 36226416
Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy.
Manitto MP, Roosing S, Boon CJ, Souied EH, Bandello F, Querques G. Manitto MP, et al. Eur J Hum Genet. 2015 Dec;23(12):1749-. doi: 10.1038/ejhg.2015.67. Epub 2015 Apr 15. Eur J Hum Genet. 2015. PMID: 25873014 Free PMC article. No abstract available.
35 results