المؤلفون: Panza E, Knowles CH, Graziano C, Thapar N, Burns AJ, Seri M, Stanghellini V, DE GIORGIO, Roberto

المساهمون: Panza, E, Knowles, Ch, Graziano, C, Thapar, N, Burns, Aj, Seri, M, Stanghellini, V, DE GIORGIO, Roberto

مصطلحات موضوعية: enteric nervous system, Enteric neuropathie, Reparative therapy, Hirschsprung’s disease, Gene mutation, GENETIC COUNSELING

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22266104; info:eu-repo/semantics/altIdentifier/wos/WOS:000301624400002; volume:96; firstpage:176; lastpage:189; numberofpages:14; journal:PROGRESS IN NEUROBIOLOGY; http://hdl.handle.net/11392/2374988Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84856998426

الإتاحة: https://doi.org/10.1016/j.pneurobio.2012.01.001Test
http://hdl.handle.net/11392/2374988Test

المؤلفون: Graziano, C, Wischmeijer, A, Pippucci, T, Fusco, C, Diquigiovanni, Chiara, Nõukas, M, Sauk, M, Kurg, A, Rivieri, F, Blau, N, Hoffmann, Gf, Chaubey, A, Schwartz, Ce, Romeo, G, Bonora, E, Garavelli, L, Seri, M.

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od_______970::2b068a5e42a65127d80126933dca828bTest
http://hdl.handle.net/2318/157229Test

المؤلفون: GARONE, CATERINA, Pippucci T, Cordelli DM, Zuntini R, Castegnaro G, Marconi C, Graziano C, Marchiani V, Verrotti A, Seri M, Franzoni E.

المساهمون: Garone C, Pippucci T, Cordelli DM, Zuntini R, Castegnaro G, Marconi C, Graziano C, Marchiani V, Verrotti A, Seri M, Franzoni E

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21592092; info:eu-repo/semantics/altIdentifier/wos/WOS:000294705000021; volume:53; firstpage:958; lastpage:961; numberofpages:3; journal:DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; http://hdl.handle.net/2318/142805Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052516570

الإتاحة: https://doi.org/10.1111/j.1469-8749.2011.03993.xTest
http://hdl.handle.net/2318/142805Test

المؤلفون: Garone C, Pippucci T, Cordelli DM, Zuntini R, Castegnaro G, Marconi C, Graziano C, Marchiani V, Seri M, Franzoni E., VERROTTI DI PIANELLA, ALBERTO

المساهمون: Garone, C, Pippucci, T, Cordelli, Dm, Zuntini, R, Castegnaro, G, Marconi, C, Graziano, C, Marchiani, V, VERROTTI DI PIANELLA, Alberto, Seri, M, Franzoni, E.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000294705000021; volume:53; firstpage:958; lastpage:961; numberofpages:4; journal:DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; http://hdl.handle.net/11391/1229962Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-80052516570

الإتاحة: http://hdl.handle.net/11391/1229962Test

المؤلفون: BRUSSINO, Alessandro, FERRONE, Marina Maria Teresa, MIGONE, Nicola, BRUSCO, Alfredo, Graziano C, Giobbe D, Dragone E, Arduino C, Lodi R, Tonon C, Gabellino AS, Rinaldi R, Miccoli S, Grosso E, Bellati MC, Orsi L

المساهمون: Brussino A, Graziano C, Giobbe D, Ferrone M.M.T., Dragone E, Arduino C, Lodi R, Tonon C, Gabellino AS, Rinaldi R, Miccoli S, Grosso E, Bellati MC, Orsi L, Migone N, Brusco A

مصطلحات موضوعية: spinocerebellar ataxia, SCA12, CAG repeat, PPP2R2B gene

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20629122; info:eu-repo/semantics/altIdentifier/wos/WOS:000280781500023; volume:25; issue:9; firstpage:1269; lastpage:1273; numberofpages:5; journal:MOVEMENT DISORDERS; http://hdl.handle.net/2318/77625Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77955075484

الإتاحة: https://doi.org/10.1002/mds.22835Test
http://hdl.handle.net/2318/77625Test

المؤلفون: Aparisi MJ, García García G, Jaijo T, Rodrigo R, Graziano C, Simsek T, Simsek E, Bernal S, Baiget M, Pérez Garrigues H, Aller E, Millán J.M., SERI, MARCO

المساهمون: Aparisi MJ, García-García G, Jaijo T, Rodrigo R, Graziano C, Seri M, Simsek T, Simsek E, Bernal S, Baiget M, Pérez-Garrigues H, Aller E, Millán JM.

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21203349; info:eu-repo/semantics/altIdentifier/wos/WOS:000286314500005; volume:16; firstpage:2948; lastpage:2954; numberofpages:7; journal:MOLECULAR VISION; http://hdl.handle.net/11585/98651Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79551708550

الإتاحة: http://hdl.handle.net/11585/98651Test

المؤلفون: Kashevarova, A., Skryabin, N., Nazarenko, L., Chechetkina, N., Salyukova, O., Tolmacheva, E., Sazhenova, E., Magini, P., Graziano, C., Romeo, G., Lebedev, I.

المصدر: European Psychiatry ; volume 29, page 1 ; ISSN 0924-9338

مصطلحات موضوعية: Psychiatry and Mental health

الإتاحة: https://doi.org/10.1016/s0924-9338Test(14)78018-6
https://api.elsevier.com/content/article/PII:S0924933814780186?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0924933814780186?httpAccept=text/plainTest

المؤلفون: Graziano C, D'Elia AV, Mazzanti L, Moscano F, Guidelli Guidi S, Scarano E, Turchetti D, Franzoni E, Romeo G, Seri M., DAMANTE, Giuseppe

المساهمون: Graziano, C, D'Elia, Av, Mazzanti, L, Moscano, F, Guidelli Guidi, S, Scarano, E, Turchetti, D, Franzoni, E, Romeo, G, Damante, Giuseppe, Seri, M.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000249144900023; volume:143A; firstpage:1802; lastpage:1805; numberofpages:4; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/11390/881479Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34547693314

الإتاحة: http://hdl.handle.net/11390/881479Test

المؤلفون: Graziano C., D'Elia A.V., Moscano F., Guidelli Guidi S., Scarano E., Damante G., MAZZANTI, LAURA, TURCHETTI, DANIELA, FRANZONI, EMILIO, ROMEO, GIOVANNI, SERI, MARCO

المساهمون: Graziano C., D'Elia AV., Mazzanti L., Moscano F., Guidelli Guidi S., Scarano E., Turchetti D., Franzoni E., Romeo G., Damante G., Seri M.

مصطلحات موضوعية: PAX6, aniridia, ataxia, mental retardation

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000249144900023; volume:143; issue:15; firstpage:1802; lastpage:1805; numberofpages:4; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/11585/48609Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34547693314

الإتاحة: https://doi.org/10.1002/ajmg.a.31808Test
http://hdl.handle.net/11585/48609Test

المؤلفون: TURCHETTI, DANIELA, ROMEO, GIOVANNI, SERI, MARCO, Razzaboni E., Zomer H., Rossi C., Ferrari S., Greco D., Graziano C.

المساهمون: Turchetti D., Razzaboni E., Zomer H., Rossi C., Ferrari S., Greco D., Graziano C., Romeo G., Seri M.

مصطلحات موضوعية: ANGELMAN SYNDROME, PRENATAL DIAGNOSIS, TERMINATION OF PREGNANCY, PSYCHOLOGICAL OUTCOME, UBE3A GENE

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000242885300010; volume:26; firstpage:1156; lastpage:1159; numberofpages:4; journal:PRENATAL DIAGNOSIS; http://hdl.handle.net/11585/36966Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33845581897

الإتاحة: https://doi.org/10.1002/pd.1577Test
http://hdl.handle.net/11585/36966Test