Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Beatrice, Felloni"'
Autor:
Filippo Muratori, Olivia Curzio, Angela Petrozzi, Giuseppe Rossi, Beatrice Felloni, Sandra Maestro, Claudia Intorcia, Helen Salsedo, Cinzia Grassi
Publikováno v:
Infant Mental Health Journal. 35:33-41
A group of 291 preschoolers consecutively enrolled at the Early Childhood Mental Health Service of IRCSS Stella Maris (Italy) were assessed using the Diagnostic Classification Zero to Three (DC:0-3; ZERO TO THREE, 1994). All active variables were ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb7988fc5d57e299b4000591eb4bcf32
https://doi.org/10.1002/imhj.21419
https://doi.org/10.1002/imhj.21419
Autor:
Sandra, Maestro, Giuseppe, Rossi, Olivia, Curzio, Beatrice, Felloni, Cinzia, Grassi, Claudia, Intorcia, Angela, Petrozzi, Helen, Salsedo, Filippo, Muratori
A group of 291 preschoolers consecutively enrolled at the Early Childhood Mental Health Service of IRCSS Stella Maris (Italy) were assessed using the Diagnostic Classification Zero to Three (DC:0-3; ZERO TO THREE, 1994). All active variables were ext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5e355d92a9f15132ff149b4be0ac1e8b
http://hdl.handle.net/11568/856780
http://hdl.handle.net/11568/856780
Autor:
Giorgio, Pini, Stefania, Bigoni, Ingegerd Witt, Engerström, Olga, Calabrese, Beatrice, Felloni, Maria Flora, Scusa, Pietro, Di Marco, Paolo, Borelli, Ubaldo, Bonuccelli, Peter O O, Julu, Jytte Bieber, Nielsen, Bodil, Morin, Stig, Hansen, Giuseppe, Gobbi, Paola, Visconti, Maria, Pintaudi, Veneselli, Edvige, Anna, Romanelli, Fabrizio, Bianchi, Manuela, Casarano, Roberta, Battini, Giovanni, Cioni, Francesca, Ariani, Alessandra, Renieri, Alberto, Benincasa, Robert S, Delamont, Michele, Zappella, Eric E J, Smeets
Publikováno v:
Neuropediatrics, 43(1), 37-43. Georg Thieme Verlag
Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively females. The Hanefeld variant, or early-onset seizure variant, has been associated with mutations in CDKL5 gene.In recent years more than 60 patients with mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0409f97ebac9c4fbd6e76388ad1f213
http://hdl.handle.net/11568/202217
http://hdl.handle.net/11568/202217