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Fabiana Mallone

Explore the profile of Fabiana Mallone including associated specialties, affiliations and a list of published articles. Areas
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Articles 28
Citations 207
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Recent Articles
1.
Mangiantini P, Mallone F, DAndrea M, Albanesi L, Lucchino L, Celli L, et al.
Clin Ophthalmol . 2025 Jan; 18:3977-3988. PMID: 39741796
Purpose: Osteogenesis imperfecta (OI) is a rare hereditary disorder of the connective tissue. Despite recent attention to corneal abnormalities in OI, understanding remains limited. This study aimed to comprehensively evaluate...
2.
Olcucu O, de Leeuw A, Lamazales L, Mallone F, Hamrah P
Cornea . 2024 Dec; PMID: 39729637
Purpose: Neuropathic corneal pain (NCP) has been recognized as a distinct disease, yet treatment options remain limited. The aim of this pilot study was to explore the effectiveness of extranasal...
3.
Nebbioso M, Mastrogiuseppe E, Gnolfo E, Artico M, Moramarco A, Mallone F, et al.
Diagnostics (Basel) . 2024 Nov; 14(21). PMID: 39518376
Objectives: Our objective was to investigate the prevalence of macular complications detected by spectral-domain optical coherence tomography (SD-OCT) in a large Caucasian cohort of RP patients, highlight the major alterations...
4.
Tirassa P, Rosso P, Fico E, Marenco M, Mallone F, Gharbiya M, et al.
Neurosci Biobehav Rev . 2024 Oct; 167:105914. PMID: 39374680
The neuropeptide Substance P (SP) and its preferred Neurokinin1 Receptor (NK1R) are known to participate in the physiopathology of neurodegenerative diseases and mainly exert a neuroprotective role. In the present...
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Di Martino V, Mallone F, Lambiase A, Celli M, Mannocci A, Celli L, et al.
Orphanet J Rare Dis . 2024 Apr; 19(1):176. PMID: 38678283
Purpose: Blue sclera is a characteristic and common clinical sign of Osteogenesis Imperfecta (OI). However, there is currently no widely accepted, objective method for assessing and grading blue sclera in...
7.
Lambiase A, Mallone F, Sacchetti M, Segatto M, Colardo M, Di Martino V, et al.
Ocul Surf . 2023 Nov; 30:295-297. PMID: 37939847
No abstract available.
8.
Mallone F, Alisi L, Lucchino L, Di Martino V, Nebbioso M, Armentano M, et al.
Int J Mol Sci . 2023 Sep; 24(17). PMID: 37686284
Neurofibromatosis type 1 (NF1) is a rare inherited neurocutaneous disorder with a major impact on the skin, nervous system and eyes. The ocular diagnostic hallmarks of this disease include iris...
9.
Lambiase A, Sacchetti M, Mallone F, Tirassa P, Greco A, Angeloni A, et al.
Biomedicines . 2022 Oct; 10(10). PMID: 36289692
The waning effectiveness of the primary vaccination for SARS-CoV-2 led to administration of an additional booster dose (BD). The efficacy of the BD in stimulating humoral systemic immune response is...
10.
Lucchino L, Mallone F, Moramarco A
Retina . 2022 Jul; 42(8):e35-e36. PMID: 35877969
No abstract available.