Falsini B - Search Results

1

A Splicing Variant in RDH8 Is Associated with Autosomal Recessive Stargardt Macular Dystrophy.

Zampatti S, Peconi C, Calvino G, Ferese R, Gambardella S, Cascella R, Sebastiani J, Falsini B, Cusumano A, Giardina E. Zampatti S, et al. Among authors: falsini b. Genes (Basel). 2023 Aug 21;14(8):1659. doi: 10.3390/genes14081659. Genes (Basel). 2023. PMID: 37628710 Free PMC article.

2

Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report.

Cusumano A, Falsini B, Giardina E, Cascella R, Sebastiani J, Marshall J. Cusumano A, et al. Among authors: falsini b. J Med Case Rep. 2019 Jan 10;13(1):5. doi: 10.1186/s13256-018-1935-1. J Med Case Rep. 2019. PMID: 30626431 Free PMC article.

3

WARE: Wet AMD Risk-Evaluation Tool as a Clinical Decision-Support System Integrating Genetic and Non-Genetic Factors.

Fabrizio C, Termine A, Caputo V, Megalizzi D, Zampatti S, Falsini B, Cusumano A, Eandi CM, Ricci F, Giardina E, Strafella C, Cascella R. Fabrizio C, et al. Among authors: falsini b. J Pers Med. 2022 Jun 24;12(7):1034. doi: 10.3390/jpm12071034. J Pers Med. 2022. PMID: 35887531 Free PMC article.

4

Longitudinal Structure-Function Evaluation in a Patient with CDHR1-Associated Retinal Dystrophy: Progressive Visual Function Loss with Retinal Remodeling.

Cusumano A, Falsini B, D'Apolito F, D'Ambrosio M, Sebastiani J, Cascella R, Barati S, Giardina E. Cusumano A, et al. Among authors: falsini b. Diagnostics (Basel). 2023 Jan 20;13(3):392. doi: 10.3390/diagnostics13030392. Diagnostics (Basel). 2023. PMID: 36766497 Free PMC article.

5

Non-Invasive High-Resolution Imaging of In Vivo Human Myelinated Axons.

Lombardo M, Cesareo M, Falsini B, Cusumano A. Lombardo M, et al. Among authors: falsini b. Diagnostics (Basel). 2024 Jan 24;14(3):253. doi: 10.3390/diagnostics14030253. Diagnostics (Basel). 2024. PMID: 38337769 Free PMC article.

6

Longitudinal Structural and Functional Evaluation of Dark-without-Pressure Fundus Lesions in Patients with Autoimmune Diseases.

Lombardo M, Ricci F, Cusumano A, Falsini B, Nucci C, Cesareo M. Lombardo M, et al. Among authors: falsini b. Diagnostics (Basel). 2024 Oct 15;14(20):2289. doi: 10.3390/diagnostics14202289. Diagnostics (Basel). 2024. PMID: 39451612 Free PMC article.

7

Ocular Involvement in Hereditary Transthyretin Amyloidosis: A Case Series Describing Novel Potential Biomarkers.

Minnella AM, Rissotto R, Maceroni M, Romano A, Fasciani R, Luigetti M, Sabatelli M, Rizzo S, Falsini B. Minnella AM, et al. Among authors: falsini b. Genes (Basel). 2021 Jun 18;12(6):927. doi: 10.3390/genes12060927. Genes (Basel). 2021. PMID: 34207092 Free PMC article.

8

Antioxidant Saffron and Central Retinal Function in ABCA4-Related Stargardt Macular Dystrophy.

Piccardi M, Fadda A, Martelli F, Marangoni D, Magli A, Minnella AM, Bertelli M, Di Marco S, Bisti S, Falsini B. Piccardi M, et al. Among authors: falsini b. Nutrients. 2019 Oct 15;11(10):2461. doi: 10.3390/nu11102461. Nutrients. 2019. PMID: 31618812 Free PMC article. Clinical Trial.

9

Ocular Involvement in Hereditary Amyloidosis.

Minnella AM, Rissotto R, Antoniazzi E, Di Girolamo M, Luigetti M, Maceroni M, Bacherini D, Falsini B, Rizzo S, Obici L. Minnella AM, et al. Among authors: falsini b. Genes (Basel). 2021 Jun 22;12(7):955. doi: 10.3390/genes12070955. Genes (Basel). 2021. PMID: 34206500 Free PMC article. Review.

10

Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.

Abed E, Placidi G, Campagna F, Federici M, Minnella A, Guerri G, Bertelli M, Piccardi M, Galli-Resta L, Falsini B. Abed E, et al. Among authors: falsini b. Clin Exp Ophthalmol. 2018 Jul;46(5):519-530. doi: 10.1111/ceo.13115. Epub 2017 Dec 28. Clin Exp Ophthalmol. 2018. PMID: 29178665

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