المؤلفون: Unger, S, Gorna, MW, Le Bechec, A, Do Vale-Pereira, S, Bedeschi, MF, Geiberger, S, Grigelioniene, G, Horemuzova, E, Lalatta, F, Lausch, E, Magnan, C, Nampoothiri, S, Nishimura, G, Petrella, D, Rojas-Ringeling, F, Utsunomiya, A, Zabel, B, Pradervand, S, Harshman, K, Campos-Xavier, B, Bonafe, L, Superti-Furga, G, Stevenson, B, Superti-Furga, A

المصدر: American journal of human genetics. 92(6):990-995

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:126853150Test

المؤلفون: Iannicelli, M, Brancati, F, Mougou-Zerelli, S, Mazzotta, A, Thomas, S, Elkhartoufi, N, Travaglini, L, Gomes, C, Ardissino, GL, Bertini, E, Boltshauser, E, Castorina, P, D'Arrigo, S, Fischetto, R, Leroy, B, Loget, P, Bonniere, M, Starck, L, Tantau, J, Gentilin, B, Majore, S, Swistun, D, Flori, E, Lalatta, F, Pantaleoni, C, Penzien, J, Grammatico, P, Dallapiccola, B, Gleeson, JG, Attie-Bitach, T, Valente, EM

المصدر: Human mutation. 31(5):E1319-E1331

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:120988936Test

المؤلفون: Provera A., Zanchi P., Silibello G., Dall'Ara F., Rigamonti C., Monti F., Ajmone P. F., Lalatta F., Costantino M. A., Vizziello P. G., Zampini L.

المساهمون: Provera, A, Zanchi, P, Silibello, G, Dall'Ara, F, Rigamonti, C, Monti, F, Ajmone, P, Lalatta, F, Costantino, M, Vizziello, P, Zampini, L

مصطلحات موضوعية: Child-directed speech, genetic syndrome, language delay, prosodic feature, sex chromosome trisomie

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000808349600001; volume:42; issue:5; firstpage:613; lastpage:627; numberofpages:15; journal:FIRST LANGUAGE; https://hdl.handle.net/10281/408057Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85131514678

الإتاحة: https://doi.org/10.1177/01427237221098553Test
https://hdl.handle.net/10281/408057Test

المؤلفون: Zampini L., Lorini A., Silibello G., Zanchi P., Dall'ara F., Ajmone P. F., Monti F., Lalatta F., Costantino M. A., Vizziello P. G.

المساهمون: Zampini, L, Lorini, A, Silibello, G, Zanchi, P, Dall'Ara, F, Ajmone, P, Monti, F, Lalatta, F, Costantino, M, Vizziello, P

مصطلحات موضوعية: Language outcome, Late-talking, Longitudinal, Predictive indice, Sex chromosome trisomie

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35162853; info:eu-repo/semantics/altIdentifier/wos/WOS:000754664500001; volume:19; issue:3; journal:INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH; http://hdl.handle.net/10281/352493Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85123932366

الإتاحة: https://doi.org/10.3390/ijerph19031831Test
http://hdl.handle.net/10281/352493Test

المؤلفون: Capelli, E, Silibello, G, Ajmone, PF, Altamore, E, Lalatta, F, Vizziello, PG, Costantino, MA, Zampini, L

المساهمون: Capelli, E, Silibello, G, Ajmone, P, Altamore, E, Lalatta, F, Vizziello, P, Costantino, M, Zampini, L

مصطلحات موضوعية: language development, longitudinal study, predictive measure, Sex chromosome trisomie

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34983283; info:eu-repo/semantics/altIdentifier/wos/WOS:000739120200001; volume:25; issue:5; firstpage:337; lastpage:348; numberofpages:12; journal:DEVELOPMENTAL NEUROREHABILITATION; http://hdl.handle.net/10281/345847Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85122313716

الإتاحة: https://doi.org/10.1080/17518423.2021.2020925Test
http://hdl.handle.net/10281/345847Test

المؤلفون: Palmieri, S., Bedeschi, M. F., Cairoli, E., Morelli, V., Lunati, M. E., Scillitani, A., Carnevale, V., Lalatta, F., Barbieri, A. M., Orsi, E., Spada, A., Chiodini, I., Eller-Vainicher, C.

المساهمون: S. Palmieri, M.F. Bedeschi, E. Cairoli, V. Morelli, M.E. Lunati, A. Scillitani, V. Carnevale, F. Lalatta, A.M. Barbieri, E. Orsi, A. Spada, I. Chiodini, C. Eller-Vainicher

مصطلحات موضوعية: bone, FGF23, phosphoru, Williams’ syndrome, endocrinology, diabetes and metabolism, Settore MED/13 - Endocrinologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30030744; info:eu-repo/semantics/altIdentifier/wos/WOS:000459901200010; journal:JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION; http://hdl.handle.net/2434/585094Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85050338588

الإتاحة: https://doi.org/10.1007/s40618-018-0924-yTest
http://hdl.handle.net/2434/585094Test

المؤلفون: Fontana, L., Bedeschi, M. F., Maitz, S., Cereda, A., Faré, C., Motta, S., Seresini, A., D’Ursi, P., Orro, A., Pecile, V., Calvello, M., Selicorni, A., Lalatta, F., Milani, D., Sirchia, S. M., Miozzo, M., Tabano, S.

المساهمون: Ministero della Salute and Regione Lombardia, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Flagship ‘InterOmics’, Fondazione Regionale per la Ricerca Biomedica

المصدر: Epigenetics ; volume 13, issue 9, page 897-909 ; ISSN 1559-2294 1559-2308

الإتاحة: https://doi.org/10.1080/15592294.2018.1514230Test

المؤلفون: Silibello G., Vizziello P., Gallucci M., Selicorni A., Milani D., Ajmone P. F., Rigamonti C., De Stefano S., Bedeschi M. F., Lalatta F.

المساهمون: Silibello, G, Vizziello, P, Gallucci, M, Selicorni, A, Milani, D, Ajmone, P, Rigamonti, C, De Stefano, S, Bedeschi, M, Lalatta, F

مصطلحات موضوعية: Child disability, Diagnosi, Lifestyle change, Parental adaptation, Public health system, Rare disease, Activities of Daily Living, Child, Female, Health Services Needs and Demand, Human, Italy, Life Style, Male, Parent, Quality of Life, Social Support, Surveys and Questionnaire, Adaptation, Psychological, Developmental Disabilitie, Disabled Children, Family Health, Rare Diseases

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27576488; info:eu-repo/semantics/altIdentifier/wos/WOS:000383540300001; volume:42; issue:1; journal:THE ITALIAN JOURNAL OF PEDIATRICS; http://hdl.handle.net/10281/285414Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84984796595

الإتاحة: https://doi.org/10.1186/s13052-016-0285-0Test
http://hdl.handle.net/10281/285414Test

المؤلفون: Zampini L., Dall'Ara F., Silibello G., Ajmone P. F., Monti F., Rigamonti C., Lalatta F., Costantino M. A., Vizziello P. G.

المساهمون: Zampini, L, Dall'Ara, F, Silibello, G, Ajmone, P, Monti, F, Rigamonti, C, Lalatta, F, Costantino, M, Vizziello, P

مصطلحات موضوعية: Diagnosis disclosure, Klinefelter syndrome, parent, prenatal diagnosi, XXY

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000635050700001; volume:50; issue:3; firstpage:324; lastpage:337; numberofpages:14; journal:CHILDREN'S HEALTH CARE; http://hdl.handle.net/10281/315505Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103415605

الإتاحة: https://doi.org/10.1080/02739615.2021.1903325Test
http://hdl.handle.net/10281/315505Test

المؤلفون: Zampini L., Burla T., Silibello G., Capelli E., Dall'Ara F., Rigamonti C., Ajmone P. F., Monti F., Zanchi P., Lalatta F., Costantino M. A., Vizziello P. G.

المساهمون: Zampini, L, Burla, T, Silibello, G, Capelli, E, Dall'Ara, F, Rigamonti, C, Ajmone, P, Monti, F, Zanchi, P, Lalatta, F, Costantino, M, Vizziello, P

مصطلحات موضوعية: babbling, Klinefelter syndrome, predictor, Preverbal, triple X syndrome, XYY syndrome

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000577500100001; volume:41; issue:2 (April 1, 2021); firstpage:200; lastpage:217; numberofpages:18; journal:FIRST LANGUAGE; http://hdl.handle.net/10281/293821Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85092317436

الإتاحة: https://doi.org/10.1177/0142723720962944Test
http://hdl.handle.net/10281/293821Test