Últimas publicaciones
Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art
2021 Oct 15;8:750586. doi: 10.3389/fmed.2021.750586. eCollection 2021. PMID: 34722588 Free PMC article. Review.
Amato A, Arrigo A, Aragona E, Manitto MP, Saladino A, Bandello F, Battaglia Parodi M. Front Med (Lausanne).
Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies
Ophthalmol Ther. 2020 Jun;9(2):249-263. doi: 10.1007/s40123-020-00241-1. Epub 2020 Mar 5. PMID: 32141037 Free PMC article. Review.
Cicinelli MV, Marchese A, Bordato A, Manitto MP, Bandello F, Battaglia Parodi M.
Benign foveal depigmentation: a multimodal imaging investigation
2023 Jan 1;17(1):74-79. doi: 10.1097/ICB.0000000000001115. PMID: 33395020
Parodi MB, Arrigo A, Bruschi E, Manitto MP, Martina E, Bandello F. Retin Cases Brief Rep.
Multimodal imaging in Schubert-Bornschein congenital stationary night blindness
2022 Oct 13:1-6. doi: 10.1080/13816810.2022.2135108. Online ahead of print. PMID: 36226416
Parodi MB, Arrigo A, Rajabian F, Mansour A, Mercuri S, Starace V, Bordato A, Manitto MP, Martina E, Bandello F. Ophthalmic Genet.
Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype
J Neuroophthalmol. 2021 Sep 1;41(3):e290-e292. doi: 10.1097/WNO.0000000000001124. PMID: 33136666 No abstract available.
Rajabian F, Manitto MP, Palombo F, Caporali L, Grazioli A, Starace V, Arrigo A, Cascavilla ML, La Morgia C, Barboni P, Bandello F, Carelli V, Battaglia Parodi M.
Morpho-functional correlation of fundus autofluorescence in Stargardt disease
Br J Ophthalmol. 2015 Oct;99(10):1354-9. doi: 10.1136/bjophthalmol-2014-306237. Epub 2015 Apr 2. PMID: 25837607
Parodi MB, Iacono P, Triolo G, La Spina C, Zucchiatti I, Cicinelli MV, Borrelli E, Manitto MP, Martina E, Bandello F.
Vascular alterations revealed with optical coherence tomography angiography in patients with choroideremia
Retina. 2019 Jun;39(6):1200-1205. doi: 10.1097/IAE.0000000000002118. PMID: 29543633 Page 2
Battaglia Parodi M, Arrigo A, MacLaren RE, Aragona E, Toto L, Mastropasqua R, Manitto MP, Bandello F.
Capillary network alterations in x-linked retinoschisis imaged on optical coherence tomography angiography
Retina. 2019 Sep;39(9):1761-1767. doi: 10.1097/IAE.0000000000002222. PMID: 29877903
Romano F, Arrigo A, Chʼng SW, Battaglia Parodi M, Manitto MP, Martina E, Bandello F, Stanga PE.
Posterior polymorphous corneal dystrophy concomitant to large colloid drusen
Eur J Ophthalmol. 2015 Mar-Apr;25(2):177-9. doi: 10.5301/ejo.5000526. Epub 2014 Oct 8. PMID: 25363852
Del Turco C, Pierro L, Querques G, Gagliardi M, Corvi F, Manitto MP, Bandello FM.
Spectral domain optical coherence tomography findings in patients with retinitis pigmentosa
Ophthalmic Res. 2013;50(3):160-4. doi: 10.1159/000351681. Epub 2013 Aug 28. PMID: 23989166
Triolo G, Pierro L, Parodi MB, De Benedetto U, Gagliardi M, Manitto MP, Bandello F.
Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy
Eur J Hum Genet. 2015 Dec;23(12):1749-. doi: 10.1038/ejhg.2015.67. Epub 2015 Apr 15. PMID: 25873014 Free PMC article. No abstract available.
Manitto MP, Roosing S, Boon CJ, Souied EH, Bandello F, Querques G.
Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches
EJIFCC. 2018 Apr 30;29(1):15-25. eCollection 2018 Apr. PMID: 29765283 Free PMC article.
Di Resta C, Spiga I, Presi S, Merella S, Pipitone GB, Manitto MP, Querques G, Parodi MB, Ferrari M, Carrera P.
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients
Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24. PMID: 22162627 Free PMC article.
Sodi A, Menchini F, Manitto MP, Passerini I, Murro V, Torricelli F, Menchini U.
De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy
Clin Chem Lab Med. 2006;44(5):533-7. doi: 10.1515/CCLM.2006.116. PMID: 16681420
Stenirri S, Battistella S, Fermo I, Manitto MP, Martina E, Brancato R, Ferrari M, Cremonesi L.