المؤلفون: Moramarco A., Lucchino L., Mallone F., Marcelli M., Alisi L., Roberti V., Giustini S., Lambiase A., Nebbioso M.

المساهمون: Moramarco, A., Lucchino, L., Mallone, F., Marcelli, M., Alisi, L., Roberti, V., Giustini, S., Lambiase, A., Nebbioso, M.

مصطلحات موضوعية: multifocal electroretinography, neurofibromatosis type 1, neurofibromin, neuroretinal function, optic pathway gliomas

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35601162; info:eu-repo/semantics/altIdentifier/wos/WOS:000801201700013; volume:15; issue:5; firstpage:773; lastpage:779; numberofpages:7; journal:INTERNATIONAL JOURNAL OF OPHTHALMOLOGY; http://hdl.handle.net/11573/1636692Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85130026685

الإتاحة: https://doi.org/10.18240/ijo.2022.05.13Test
http://hdl.handle.net/11573/1636692Test

المؤلفون: Moramarco A, Alisi L, Lambiase A, Giustini S, Lucchino L, Miraglia E, Roberti V, Nebbioso M

المصدر: Eye and Brain, Vol Volume 13, Pp 71-78 (2021)

مصطلحات موضوعية: gorlin-goltz syndrome, nevoid basal cell carcinoma syndrome, pattern visual evoked potentials, rare diseases, electrophysiology, visual pathway, genodermatosis, patch1, Ophthalmology, RE1-994, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

العلاقة: https://www.dovepress.com/electrophysiological-study-of-visual-pathways-in-nevoid-basal-cell-car-peer-reviewed-article-EBTest; https://doaj.org/toc/1179-2744Test

الوصول الحر: https://doaj.org/article/3b7eb313311a490095f670a19247d685Test

المؤلفون: Moramarco A., Mallone F., Sacchetti M., Lucchino L., Miraglia E., Roberti V., Lambiase A., Giustini S.

المساهمون: Moramarco, A., Mallone, F., Sacchetti, M., Lucchino, L., Miraglia, E., Roberti, V., Lambiase, A., Giustini, S.

مصطلحات موضوعية: choroidal nodule, enhanced depth imaging OCT (EDI-OCT), hyperpigmented spots (HSs), indirect ophthalmoscopy, near-infrared reflectance (NIR) imaging OCT (NIR-OCT), neurofibromatosis type I (NF1), rare disease, ultra-wide field (UWF)

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33757576; info:eu-repo/semantics/altIdentifier/wos/WOS:000632957400001; volume:16; issue:1; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/11573/1533645Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103174540

الإتاحة: https://doi.org/10.1186/s13023-021-01773-wTest
http://hdl.handle.net/11573/1533645Test