Pubblicazioni

An update on choroidal abnormalities and retinal microvascular changes in neurofibromatosis type 1

2022 - ORPHANET JOURNAL OF RARE DISEASES
Mallone, Fabiana; Lucchino, Luca; Giustini, Sandra; Lambiase, Alessandro; Moramarco, Antonietta

Expert opinion of an Italian working group on the assessment of cognitive, psychological, and neurological outcomes in pediatric, adolescent, and adult patients with phenylketonuria

2022 - ORPHANET JOURNAL OF RARE DISEASES
Manti, Filippo; Caviglia, Stefania; Cazzorla, Chiara; Dicintio, Annamaria; Pilotto, Andrea; Burlina, Alessandro P

Long-term clinical efficacy of topical treatment with recombinant human nerve growth factor in neurotrophic keratopathy: a novel cure for a rare degenerative corneal disease?

2022 - ORPHANET JOURNAL OF RARE DISEASES
Bruscolini, A.; Marenco, M.; Albanese, G. M.; Lambiase, A.; Sacchetti, M.

Autophagy-lysosome pathway alteration in ocular surface manifestations in Fabry disease patients

2022 - ORPHANET JOURNAL OF RARE DISEASES
Marenco, M.; Segatto, M.; Sacchetti, M.; Mangiantini, P.; Giovannetti, F.; Plateroti, R.

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