Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Valerio Di Martino"'
Autor:
Valerio Di Martino, Fabiana Mallone, Alessandro Lambiase, Mauro Celli, Alice Mannocci, Luca Celli, Pietro Mangiantini, Pasquale Fino, Antonietta Moramarco
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract 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 individuals with OI. To address this
Externí odkaz:
https://doaj.org/article/6d2ef98797d14cce894ed3b6d9ce848d
Autor:
Fabiana Mallone, Ludovico Alisi, Luca Lucchino, Valerio Di Martino, Marcella Nebbioso, Marta Armentano, Alessandro Lambiase, Antonietta Moramarco
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 17, p 13481 (2023)
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 Lisch nodules, ocular and eyelid neurofibromas, eyelid c
Externí odkaz:
https://doaj.org/article/a5948e8f0d9e4faf915845d4ce26d0f4
Autor:
Marta Armentano, Luca Lucchino, Ludovico Alisi, Antonio Valerio Chicca, Valerio Di Martino, Emanuele Miraglia, Ludovico Iannetti, Anna Maria Comberiati, Sandra Giustini, Alessandro Lambiase, Antonietta Moramarco
Publikováno v:
Applied Sciences, Vol 13, Iss 10, p 6304 (2023)
Neurofibromatosis type 2 (NF2) is a genetically determined tumor-predisposing syndrome. Ocular manifestations include cataracts, epiretinal membranes, retinal hamartomas, optic disk gliomas, and optic nerve sheath meningiomas. Moreover, optic disk ed
Externí odkaz:
https://doaj.org/article/cd6703b80b1e4ad28f5fd05701290829