المؤلفون: Ceravolo I., Mannino F., Irrera N., Minutoli L., Arcoraci V., Altavilla D., Cavallini G. M., Guarini S., Squadrito F., Pallio G.

المساهمون: Ceravolo, I., Mannino, F., Irrera, N., Minutoli, L., Arcoraci, V., Altavilla, D., Cavallini, G. M., Guarini, S., Squadrito, F., Pallio, G.

مصطلحات موضوعية: apoptosi, Fuchs endothelial corneal dystrophy, inflammation, oxidative stre, polydeoxyribonucleotide, ROS

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35455444; info:eu-repo/semantics/altIdentifier/wos/WOS:000785672100001; volume:15; issue:4; firstpage:1; lastpage:12; journal:PHARMACEUTICALS; http://hdl.handle.net/11380/1279846Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85128306472

الإتاحة: https://doi.org/10.3390/ph15040447Test
http://hdl.handle.net/11380/1279846Test

المؤلفون: Ceravolo I., Oliverio G. W., Alibrandi A., Bhatti A., Trombetta L., Rejdak R., Toro M. D., Trombetta C. J.

المساهمون: Ceravolo, I., Oliverio, G. W., Alibrandi, A., Bhatti, A., Trombetta, L., Rejdak, R., Toro, M. D., Trombetta, C. J.

مصطلحات موضوعية: Biomarker, Diabetic macular edema, Inflammation, Optical coherence tomography

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000553476900001; volume:10; issue:6; firstpage:413; journal:DIAGNOSTICS; http://hdl.handle.net/11588/892657Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85086875569

الإتاحة: https://doi.org/10.3390/diagnostics10060413Test
http://hdl.handle.net/11588/892657Test

المؤلفون: Casto, C, Dipasquale, V, Ceravolo, I, Gambadauro, A, Aliberto, E, Galletta, K, Granata, F, Ceravolo, G, Falzia, E, Riva, A, Piccolo, G, Cutrupi, MC, Striano, P, Accogli, A, Zara, F, Di Rosa, G, Gitto, E, Calì, E, Efthymiou, S, Salpietro, V, Houlden, H, Chimenz, R

المصدر: Brain Sciences , 11 (9) , Article 1150. (2021)

مصطلحات موضوعية: genotype, motor impairment, Nance-Horan syndrome, next-generation sequencing, congenital cataracts, dental anomalies, pediatric age

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10134371/1/brainsci-11-01150.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10134371Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10134371/1/brainsci-11-01150.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10134371Test/

المؤلفون: Cuppari, C, Salpietro, A, Chimenz, R, Colavita, L, Ceravolo, MD, Gitto, E, Sallemi, A, Fusco, M, Ceravolo, I, Farello, G, Iapadre, G, Rocca, C, Salazar, A, Mancuso, A

المساهمون: Cuppari, C, Salpietro, A, Chimenz, R, Colavita, L, Ceravolo, Md, Gitto, E, Sallemi, A, Fusco, M, Ceravolo, I, Farello, G, Iapadre, G, Rocca, C, Salazar, A, Mancuso, A

مصطلحات موضوعية: Joubert syndrome, anomalies oral-facial-digital, neurological anomalies

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000894484100007; volume:21; issue:01; firstpage:58; lastpage:61; numberofpages:4; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3271877Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85144846794

الإتاحة: https://doi.org/10.1055/s-0042-1759516Test
https://hdl.handle.net/11570/3271877Test

المؤلفون: Manti, S, Gitto, E, Ceravolo, I, Mancuso, A, Ceravolo, A, Salpietro, A, Farello, G, Chimenz, R, Iapadre, G, Battaglia, F, Cuppari, C

المساهمون: Manti, S, Gitto, E, Ceravolo, I, Mancuso, A, Ceravolo, A, Salpietro, A, Farello, G, Chimenz, R, Iapadre, G, Battaglia, F, Cuppari, C

مصطلحات موضوعية: emergencie, Joubert syndrome, multiorgan involvement

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000908440600001; volume:21; issue:01; firstpage:3; lastpage:7; numberofpages:5; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3271873Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85146703871

الإتاحة: https://doi.org/10.1055/s-0042-1760240Test
https://hdl.handle.net/11570/3271873Test

المؤلفون: La Macchia, T, Mancuso, A, Ceravolo, MD, Cuppari, C, Chimenz, R, Farello, G, Gitto, E, Iapadre, G, Ceravolo, I

المساهمون: La Macchia, T, Mancuso, A, Ceravolo, Md, Cuppari, C, Chimenz, R, Farello, G, Gitto, E, Iapadre, G, Ceravolo, I

مصطلحات موضوعية: Alstrom syndrome, ciliopathie, ALMS1, Bardet-Biedl syndrome, obesity

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000894484100001; volume:21; issue:01; firstpage:15; lastpage:17; numberofpages:3; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3271874Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85144891809

الإتاحة: https://doi.org/10.1055/s-0042-1759535Test
https://hdl.handle.net/11570/3271874Test

المؤلفون: Di Bartolomeo, L, Ceravolo, I, Borgia, F, Vaccaro, F, Guarneri, C, Vaccaro, M

المساهمون: Di Bartolomeo, L, Ceravolo, I, Borgia, F, Vaccaro, F, Guarneri, C, Vaccaro, M

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36808348; info:eu-repo/semantics/altIdentifier/wos/WOS:000942632200024; volume:27; issue:3; firstpage:1023; lastpage:1026; numberofpages:4; journal:EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES; https://hdl.handle.net/11570/3253976Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85148678996

الإتاحة: https://doi.org/10.26355/eurrev_202302_31197Test
https://hdl.handle.net/11570/3253976Test

المؤلفون: Ceravolo, I, Granata, F, Gitto, E, Iapadre, G, Chimenz, R, Giannitto, N, Mancuso, A, Ceravolo, MD, La Macchia, T, Rissotto, F, Farello, G, Cuppari, C

المساهمون: Ceravolo, I, Granata, F, Gitto, E, Iapadre, G, Chimenz, R, Giannitto, N, Mancuso, A, Ceravolo, Md, La Macchia, T, Rissotto, F, Farello, G, Cuppari, C

مصطلحات موضوعية: Joubert syndrome, genetic classification, ophthalmological abnormalities

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000894484100008; volume:21; issue:01; firstpage:68; lastpage:72; numberofpages:5; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3271875Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85144869110

الإتاحة: https://doi.org/10.1055/s-0042-1759536Test
https://hdl.handle.net/11570/3271875Test

المؤلفون: Scuderi A, Prato A, Dicanio D, Spoto G, Salpietro V, Ceravolo G, Granata F, Farello G, Iapadre G, Zagaroli L, Nanni G, Ceravolo I, Pironti E, Amore G, Di Rosa G

المساهمون: Scuderi, A, Prato, A, Dicanio, D, Spoto, G, Salpietro, V, Ceravolo, G, Granata, F, Farello, G, Iapadre, G, Zagaroli, L, Nanni, G, Ceravolo, I, Pironti, E, Amore, G, Di Rosa, G

مصطلحات موضوعية: neurodevelopment age-related onset Joubert syndrome

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000894484100005; volume:21; issue:01; firstpage:8; lastpage:14; numberofpages:7; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3272980Test

الإتاحة: https://doi.org/10.1055/s-0042-1759539Test
https://hdl.handle.net/11570/3272980Test

المؤلفون: Amore, G, Spoto, G, Scuderi, A, Prato, A, Dicanio, D, Nicotera, A, Farello, G, Chimenz, R, Ceravolo, I, Salpietro, V, Gitto, E, Ceravolo, G, Iapadre, G, Rosa, GD, Pironti, E

المساهمون: Amore, G, Spoto, G, Scuderi, A, Prato, A, Dicanio, D, Nicotera, A, Farello, G, Chimenz, R, Ceravolo, I, Salpietro, V, Gitto, E, Ceravolo, G, Iapadre, G, Rosa, Gd, Pironti, E

مصطلحات موضوعية: Bardet-Biedl syndrome, ciliopathie, clinical feature, BBS genes

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000894484100002; volume:21; issue:01; firstpage:33; lastpage:40; numberofpages:8; journal:JOURNAL OF PEDIATRIC NEUROLOGY; https://hdl.handle.net/11570/3271876Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85144851100

الإتاحة: https://doi.org/10.1055/s-0042-1759534Test
https://hdl.handle.net/11570/3271876Test