المؤلفون: Costanza J., Camanni M., Ferrari M. M., De Cosmi V., Tabano S., Fontana L., Radaelli T., Privitera G., Alberico D., Colapietro P., Motta S., Sirchia S., Stampalija T., Tabasso C., Roggero P., Parazzini F., Mosca F., Ferrazzi E., Bosari S., Miozzo M., Agostoni C.

المساهمون: Costanza, J., Camanni, M., Ferrari, M. M., De Cosmi, V., Tabano, S., Fontana, L., Radaelli, T., Privitera, G., Alberico, D., Colapietro, P., Motta, S., Sirchia, S., Stampalija, T., Tabasso, C., Roggero, P., Parazzini, F., Mosca, F., Ferrazzi, E., Bosari, S., Miozzo, M., Agostoni, C.

مصطلحات موضوعية: n/a

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34344991; info:eu-repo/semantics/altIdentifier/wos/WOS:000680759200001; volume:91; issue:7; firstpage:1890; lastpage:1896; numberofpages:7; journal:PEDIATRIC RESEARCH; http://hdl.handle.net/11368/2993922Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85111928550; https://www.nature.com/articles/s41390-021-01665-6Test

الإتاحة: https://doi.org/10.1038/s41390-021-01665-6Test
http://hdl.handle.net/11368/2993922Test
https://www.nature.com/articles/s41390-021-01665-6Test

المؤلفون: Nicolì V., Tabano S. M., Colapietro P., Maestri M., Ricciardi R., Stoccoro A., Fontana L., Guida M., Miozzo M., Coppede' F., Migliore L.

المساهمون: Nicolì, V., Tabano, S. M., Colapietro, P., Maestri, M., Ricciardi, R., Stoccoro, A., Fontana, L., Guida, M., Miozzo, M., Coppede', F., Migliore, L.

مصطلحات موضوعية: myasthenia gravi, X chromosome inactivation, skewed XCI, gender bia, gender medicine, autoimmune disease, neuromuscular disease, HUMARA, epigenetics

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000786785400001; volume:13; issue:4; numberofpages:13; journal:GENES; https://hdl.handle.net/11568/1148739Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85129121616; https://www.mdpi.com/2073-4425/13/4/696Test

الإتاحة: https://doi.org/10.3390/genes13040696Test
https://hdl.handle.net/11568/1148739Test
https://www.mdpi.com/2073-4425/13/4/696Test

المؤلفون: Pescia, C, Pini, G, Tabano, S, Berti, E, Alberti Violetti, S, Croci, G A

المساهمون: C. Pescia, G. Pini, S. Tabano, E. Berti, S. Alberti Violetti, G.A. Croci

مصطلحات موضوعية: Settore MED/08 - Anatomia Patologica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38334200; info:eu-repo/semantics/altIdentifier/wos/WOS:001160667400001; firstpage:1; lastpage:4; numberofpages:4; journal:JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY; https://hdl.handle.net/2434/1028730Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85184915080

الإتاحة: https://doi.org/10.1111/jdv.19845Test
https://hdl.handle.net/2434/1028730Test

المؤلفون: Malacrida A., Di Domizio A., Bentivegna A., Cislaghi G., Messuti E., Tabano S. M., Giussani C., Zuliani V., Rivara M., Nicolini G.

المساهمون: A. Malacrida, A. Di Domizio, A. Bentivegna, G. Cislaghi, E. Messuti, S.M. Tabano, C. Giussani, V. Zuliani, M. Rivara, G. Nicolini

مصطلحات موضوعية: ALKBH2, Glioblastoma, Patient-derived GSC, Temozolomide, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35053068; info:eu-repo/semantics/altIdentifier/wos/WOS:000750725800001; volume:11; issue:1; firstpage:1; lastpage:15; numberofpages:15; journal:BIOLOGY; http://hdl.handle.net/2434/904028Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85122205234

الإتاحة: https://doi.org/10.3390/biology11010070Test
http://hdl.handle.net/2434/904028Test

المؤلفون: Tabano S, Tassi L, Cannone MG, Brescia G, Gaudioso G, Ferrara M, Colapietro P, Fontana L, Miozzo MR, Croci GA, Seia M, Piuma C, Solbiati M, Tobaldini E, Ferrero S, Montano N, Costantino G, Buoli M

المساهمون: S. Tabano, L. Tassi, M. Cannone, G. Brescia, G. Gaudioso, M. Ferrara, P. Colapietro, L. Fontana, M. Miozzo, G. Croci, M. Seia, C. Piuma, M. Solbiati, E. Tobaldini, S. Ferrero, N. Montano, G. Costantino, M. Buoli

مصطلحات موضوعية: COVID-19, Epigenetic, Health professional, Mental health, Stress-related genes, Settore MED/25 - Psichiatria, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36001138; info:eu-repo/semantics/altIdentifier/wos/WOS:000844424700003; journal:EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE; https://hdl.handle.net/2434/936880Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85136573518

الإتاحة: https://doi.org/10.1007/s00406-022-01472-yTest
https://hdl.handle.net/2434/936880Test

المؤلفون: Cerrato F., Sparago A., Ariani F., Brugnoletti F., Calzari L., Coppede F., De Luca A., Gervasini C., Giardina E., Gurrieri F., Nigro C. L., Merla G., Miozzo M., Russo S., Sangiorgi E., Sirchia S. M., Squeo G. M., Tabano S., Tabolacci E., Torrente I., Genuardi M., Neri G., Riccio A.

المساهمون: Cerrato, F., Sparago, A., Ariani, F., Brugnoletti, F., Calzari, L., Coppede, F., De Luca, A., Gervasini, C., Giardina, E., Gurrieri, F., Nigro, C. L., Merla, G., Miozzo, M., Russo, S., Sangiorgi, E., Sirchia, S. M., Squeo, G. M., Tabano, S., Tabolacci, E., Torrente, I., Genuardi, M., Neri, G., Riccio, A.

مصطلحات موضوعية: Developmental delay/intellectual disability disorder, DNA methylation, Epi-signature, Genetic testing, Hereditary tumor, High-throughput analysi, Imprinting disorder, Neuromuscular disease, Prenatal diagnosis

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32224912; info:eu-repo/semantics/altIdentifier/wos/WOS:000537224600081; volume:11; issue:4; firstpage:355; numberofpages:30; journal:GENES; https://hdl.handle.net/11568/1041052Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85082574850; https://www.mdpi.com/2073-4425/11/4/355Test

الإتاحة: https://doi.org/10.3390/genes11040355Test
https://hdl.handle.net/11568/1041052Test
https://www.mdpi.com/2073-4425/11/4/355Test

المؤلفون: Pizzi M., Croci G. A., Ruggeri M., Tabano S., Dei Tos A. P., Sabattini E., Gianelli U.

المساهمون: M. Pizzi, G.A. Croci, M. Ruggeri, S. Tabano, A.P. Dei To, E. Sabattini, U. Gianelli

مصطلحات موضوعية: MPN-U, myeloid disorder, myeloproliferative neoplasm, WHO classification, Settore MED/08 - Anatomia Patologica, Settore MED/03 - Genetica Medica, Settore MED/15 - Malattie del Sangue

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34830822; info:eu-repo/semantics/altIdentifier/wos/WOS:000725140700001; volume:13; issue:22; firstpage:1; lastpage:21; numberofpages:21; journal:CANCERS; http://hdl.handle.net/2434/904040Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85118861615

الإتاحة: https://doi.org/10.3390/cancers13225666Test
http://hdl.handle.net/2434/904040Test

المؤلفون: Fontana L., Tabano S., Maitz S., Colapietro P., Garzia E., Gerli A. G., Sirchia S. M., Miozzo M.

المساهمون: L. Fontana, S. Tabano, S. Maitz, P. Colapietro, E. Garzia, A.G. Gerli, S.M. Sirchia, M. Miozzo

مصطلحات موضوعية: Beckwith-Wiedemann syndrome, Clinical diagnosi, Discordant monozygotic twin, Molecular testing, Multilocus imprinting disturbance, X-chromosome inactivation, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33810554; info:eu-repo/semantics/altIdentifier/wos/WOS:000638646600001; volume:22; issue:7; firstpage:1; lastpage:20; numberofpages:20; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2434/851677Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103053768

الإتاحة: https://doi.org/10.3390/ijms22073445Test
http://hdl.handle.net/2434/851677Test

المؤلفون: Rondinone O., Murgia A., Costanza J., Tabano S., Camanni M., Corsaro L., Fontana L., Colapietro P., Calzari L., Motta S., Santaniello C., Radaelli T., Ferrazzi E., Bosari S., Gentilini D., Sirchia S. M., Miozzo M.

المساهمون: O. Rondinone, A. Murgia, J. Costanza, S. Tabano, M. Camanni, L. Corsaro, L. Fontana, P. Colapietro, L. Calzari, S. Motta, C. Santaniello, T. Radaelli, E. Ferrazzi, S. Bosari, D. Gentilini, S.M. Sirchia, M. Miozzo

مصطلحات موضوعية: birth weight, LINE-1, methylome, normal pregnancie, placenta, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33669975; info:eu-repo/semantics/altIdentifier/wos/WOS:000623926500001; volume:22; issue:4; firstpage:1; lastpage:19; numberofpages:19; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/2434/826856Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85100921870

الإتاحة: https://doi.org/10.3390/ijms22042136Test
http://hdl.handle.net/2434/826856Test

المؤلفون: Cattaneo D., Croci G. A., Bucelli C., Tabano S., Cannone M. G., Gaudioso G., Barbanti M. C., Barbullushi K., Bianchi P., Fermo E., Fabris S., Baldini L., Gianelli U., Iurlo A.

المساهمون: D. Cattaneo, G.A. Croci, C. Bucelli, S. Tabano, M.G. Cannone, G. Gaudioso, M.C. Barbanti, K. Barbullushi, P. Bianchi, E. Fermo, S. Fabri, L. Baldini, U. Gianelli, A. Iurlo

مصطلحات موضوعية: bone marrow morphology, essential thrombocytemia, next-generation sequencing, prognosi, triple-negative, Settore MED/15 - Malattie del Sangue

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33791220; info:eu-repo/semantics/altIdentifier/wos/WOS:000632868400001; volume:11; firstpage:1; lastpage:10; numberofpages:10; journal:FRONTIERS IN ONCOLOGY; https://hdl.handle.net/2434/859576Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103322206

الإتاحة: https://doi.org/10.3389/fonc.2021.637116Test
https://hdl.handle.net/2434/859576Test