Retinal vascular density in multiple sclerosis: a one year follow up

Autor: Lanzillo, R, Cennamo, G, Moccia, M, Criscuolo, C, Carotenuto, A, Frattaruolo, N, Sparnelli, F, MELENZANE, ANTONIETTA, Lamberti, A, Servillo, G, Tranfa, F, De Crecchio, G, Brescia Morra, V

Vascular pathology is increasingly acknowledged as a risk factor of multiple sclerosis (MS). Vascular density (VD) is reduced in MS patients' eyes on optical coherence tomography (OCT) angiography (A).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::4c9abea368a24d2b592377c63fadbf11
http://hdl.handle.net/11588/720288

Retinal degeneration associated with ectopia lentis.

Autor: Simonelli, F.¹, De Crecchio, G.², Testa, F.¹, Nunziata, G.¹, Mazzeo, S.¹, Romano, N.¹, Cavaliere, L.³, Rinaldi, M.M.³, Rinaldi, E.¹

Publikováno v: Ophthalmic Genetics. Jun99, Vol. 20 Issue 2, p121-126. 6p. 2 Black and White Photographs, 2 Diagrams, 1 Chart.

Superficial Annular Corneal Dystrophy, Ichthyosis nigrans, Microcephaly and Mild Mental Subnormality.

Autor: Sammartino, A.¹, De Crecchio, G.¹, Federico, A.², Loffredo, A.

Publikováno v: Ophthalmologica. 1982, Vol. 185 Issue 4, p226-230. 5p.

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

Autor: de Crecchio G, Simonelli F, Nunziata G, Mazzeo S, Greco GM, Rinaldi E, Ventruto V, Ciccodicola A, Miano MG, Testa F, Curci A, D'Urso M, Rinaldi MM, Cavaliere ML, Castelluccio P, Cennamo G, Cesarano I, Vecchio EC, Reibaldi M, DE CRECCHIO, GIUSEPPE

Publikováno v: Clinical genetics (Online) 54 (1998): 315–320.
info:cnr-pdr/source/autori:de Crecchio G, Simonelli F, Nunziata G, Mazzeo S, Greco GM, Rinaldi E, Ventruto V, Ciccodicola A, Miano MG, Testa F, Curci A, D'Urso M, Rinaldi MM, Cavaliere ML, Castelluccio P./titolo:Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity./doi:/rivista:Clinical genetics (Online)/anno:1998/pagina_da:315/pagina_a:320/intervallo_pagine:315–320/volume:54

Two unrelated families with familial exudative vitreoretinopathy (FEVR) show apparent autosomal recessive inheritance rather than the previously reported autosomal dominant or X-linked recessive mode of inheritance. Compared with the other modes of i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0a43ddebd92c9fdb9c18884dfa0e3f5
http://hdl.handle.net/11588/490632

Aberrant congenital macular vessel crossing the fovea: evaluation with optical coherence tomography.

Autor: de Crecchio, G.¹ crecchio@unina.it, Pappalardo, G.¹, Pascotto, F.², Forte, R.¹

Publikováno v: Eye. Dec2006, Vol. 20 Issue 12, p1464-1466. 3p. 1 Color Photograph.