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Orphanet Journal of Rare Diseases|March 24, 2021
Hyperpigmented spots at fundus examination: a new ocular sign in Neurofibromatosis Type IAntonietta Moramarco, Fabiana Mallone, Marta Sacchetti, et al.
The British Journal of Ophthalmology|December 10, 2014
Morphologic and vasculature features of the choroid and associated choroid-retinal thickness alterations in neurofibromatosis type 1Solmaz Abdolrahimzadeh, Lorenzo Felli, Rocco Plateroti, et al.
The British Journal of Ophthalmology|February 2, 2019
Retinal microvascular abnormalities in neurofibromatosis type 1Antonietta Moramarco, Emanuele Miraglia, Fabiana Mallone, et al.
Eye and Brain|April 7, 2021
Electrophysiological Study of Visual Pathways in Nevoid Basal Cell Carcinoma Syndrome PatientsAntonietta Moramarco, Ludovico Alisi, Alessandro Lambiase, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletionIrene Bottillo, Isabella Torrente, Valentina Lanari, et al.
Orphanet Journal of Rare Diseases|September 20, 2019
Ocular manifestations in Gorlin-Goltz syndromeAntonietta Moramarco, Ehud Himmelblau, Emanuele Miraglia, et al.
International Journal of Ophthalmology|May 23, 2022
Neuroretinal dysfunction in patients affected by neurofibromatosis type 1Antonietta Moramarco, Luca Lucchino, Fabiana Mallone, et al.
Eye and Brain|October 29, 2020
Neurofibromatosis Type 1: Ocular Electrophysiological and Perimetric AnomaliesMarcella Nebbioso, Antonietta Moramarco, Alessandro Lambiase, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromasAlessandro De Luca, Laura Bernardini, Caterina Ceccarini, et al.
Italian Journal of Dermatology and Venereology|July 29, 2024
Comprehensive analysis of pseudoxanthoma elasticum: epidemiological, genetic, and clinical findings from the leading Italian centerAlessandro Laghi, Victor D Mandel, Ilaria Zubba, et al.
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